Single Crystal Diamond Dies Packaged with Ultrathin Pocketed Semiconductor Wafer

Abstract

A reconstituted wafer product includes diamond dies sandwiched between a first wafer and a second wafer in a manner that provides a thermally conductive connection between the first wafer and second wafer through the diamond dies. At least one of the first wafer and second wafer includes pockets containing one or more diamond dies. An alternative reconstituted wafer product may include diamond dies attached to a silicon wafer in a manner that provides a thermally conductive connection between the wafer and the diamond dies, wherein the silicon wafer is bonded to the dies in areas that include one or more areas of recrystallized silicon.

Claims

1. A reconstituted wafer product, comprising: a plurality of dies containing diamond sandwiched between a first wafer and a second wafer in a manner that provides a thermally conductive connection between the first wafer and second wafer through the dies containing diamond, where at least one of the first wafer and second wafer includes pockets containing one or more dies containing diamond.

2. The product of claim 1 where the pockets are created in a top layer of the first wafer, or the second wafer or both the first wafer and the second wafer.

3. The product of claim 2 wherein the top layer contains at least one of the following materials: silicon, germanium, aluminum, tin, copper, silver, gold, zinc, silicon oxide, a sol-gel, polymer, thermoplastic, curable adhesive, molding compound, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, spin-on glass, polymer-derived ceramics, silicones, and polyimides.

4. The product of claim 1 where at least one of the first wafer and the second wafer is a silicon wafer and the pockets are created in the silicon wafer.

5. The product of claim 1 where the pockets are created by additive manufacturing.

6. The product of claim 1 wherein the pockets each envelope at least 90 percent of each of the plurality of dies containing diamond.

7. The product of claim 1 wherein the pockets extend 100 micrometers or deeper into at least one of the first wafer and second wafer.

8. The product of claim 1 wherein the pockets extend less than 100 micrometers but greater than 10 micrometers into at least one of the first wafer and second wafer.

9. The product of claim 1, wherein the thermal resistance of the reconstituted wafer product is less than 2 mm.sup.2-K/W when integrated into a final chip package.

10. The product of claim 1, wherein the thermal resistance of the reconstituted wafer product is less than 1 mm.sup.2-K/W when integrated into a final chip package.

11. The product of claim 1, wherein the thermal resistance of the reconstituted wafer product is less than 0.5 mm.sup.2-K/W when integrated into a final chip package.

12. The product of claim 1, wherein the dies containing diamond include one or more single crystal diamond (SCD) dies.

13. The product of claim 12, wherein the dies containing diamond are all SCD dies.

14. The product of claim 12, wherein the one or more SCD dies are characterized by a lateral dimension of 1 centimeter or greater.

15. The product of claim 1, wherein the dies containing diamond include at least one polycrystalline diamond die.

16. The product of claim 1, wherein the dies containing diamond include at least one composite diamond die comprised of diamond and a metal, wherein the metal includes one or more of the following: copper, silver, gold, aluminum, and zinc.

17. The product of claim 1, wherein at least one of the dies containing diamond has a roughness on at least one side of at least 2 nanometers.

18. The product of claim 1, wherein first and second wafers are characterized by lateral dimensions corresponding to those of a standard-sized semiconductor wafer.

19. The product of claim 1, wherein the first and second wafers are silicon wafers.

20. The product of claim 1, wherein at least one of the first and second wafers is characterized by a thickness of less than 100 micrometers.

21. The product of claim 1, wherein at least one of the first and second wafers is characterized by a thickness of less than 10 micrometers.

22. The product of claim 1, wherein a layer of copper, aluminum, or silicon carbide is sandwiched between the dies containing diamond and a first wafer, wherein the copper, aluminum, or silicon carbide, is at least 100 micrometers thick.

23. The product of claim 1 wherein the dies containing diamond are attached to either: the first wafer, the second wafer, or both wafers by either: thermocompression bonding (TCB), soldering, eutectic bonding, transient liquid phase bonding (TLPB), sintering, surface activated bonding (SAB), atomic diffusion bonding (ADB), plasma assisted bonding (PAB), ultrasonic bonding (UB), brazing, or adhesive bonding.

24. The product of claim 1 wherein the at least one side of each of the dies containing diamond is coated with a smoothening material.

25. The product of claim 24 wherein the smoothening material is a metal and the dies containing diamond are attached to either: the first wafer, the second wafer or both wafers, by thermocompression bonding (TCB), soldering, eutectic bonding, transient liquid phase bonding (TLPB), sintering, surface activated bonding (SAB), atomic diffusion bonding (ADB), plasma assisted bonding (PAB), laser assisted bonding (LAB), Flash Lamp assisted bonding (FLAB), ultrasonic bonding (UB), brazing, or adhesive bonding.

26. The product of claim 1 wherein either the first wafer, the second wafer, or both the first wafer and the second wafer are silicon wafers bonded to the dies containing diamond by surface melting the first wafer, the second wafer or both the first wafer and the second wafer.

27. The product of claim 26 wherein the dies containing diamond each have a mean surface roughness on at least one side of at least 2 nanometers.

28. The product of claim 1 wherein either the first wafer, the second wafer, or both wafers are bonded to the dies containing diamond with a multi-layer material made out of nickel and aluminum, aluminum and titanium, titanium and silicon, boron and titanium, or aluminum and palladium.

29. The product of claim 1 further comprising a smoothening material coupled to each of the plurality of dies containing diamond, wherein the smoothening material is a semiconductor smoothening layer and the dies containing diamond are attached to either: the first wafer, the second wafer, or both wafers by either: surface activated bonding (SAB), atomic diffusion bonding (ADB), plasma assisted bonding (PAB), laser assisted bonding (LAB), Flash Lamp assisted bonding (FLAB), or adhesive bonding.

30. The product of claim 29 wherein the smoothening material is a dielectric and the dies containing diamond are attached to either: the first wafer, the second wafer, or both wafers by either: surface activated bonding (SAB), atomic diffusion bonding (ADB), plasma assisted bonding (PAB), or adhesive bonding.

31. The product of claim 1, wherein the dies containing diamond are attached to either: the first wafer, the second wafer, or both wafers using a bond material.

32. The product of claim 31, wherein the bond material includes copper, silicon, or a dielectric.

33. The product of claim 1, wherein gaps between adjacent dies containing diamond of the plurality of dies containing diamond are partially or completely filled with a gap-filling material.

34. The product of claim 33, wherein the gap-filling material includes spin-on-glass.

35. The product of claim 33, wherein the gap-filling material includes a through-hole wafer.

36. The product of claim 33, wherein the gaps are filled by a powder, and the powder is either sintered or partially or completely molten.

37. The product of claim 33, wherein the gaps are filled by a composite of a powder and either a curable adhesive or thermoplastic.

38. The product of claim 33, wherein the gap-filling material includes one or more of the following: a sol-gel, oxide powder, silicon powder, silicon carbide powder, copper powder, silver powder, carbon powder, solder, eutectic, brazing material, transient liquid phase precursors mixture, polymer, thermoplastic, curable adhesive, molding compound, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, polymer-derived ceramics, silicones, polybenzimidazole, and polyimides.

39. The product of claim 1 wherein at least one of the plurality of dies containing diamond are located in an area of the reconstituted wafer product corresponding to a hot spot in one or more logic elements when the reconstituted wafer product is bonded with the one or more logic elements.

40. The product of claim 1, wherein at least one of the plurality of dies containing diamond is located in an area of the reconstituted wafer product corresponding to the location of one or more logic elements that are known good dies when the reconstituted wafer product is bonded with the one or more logic elements.

41. The product of claim 1 further comprising one or more dummy dies sandwiched between the first and second wafer wherein the dummy dies are placed on locations corresponding to one or more logic elements that are not known good dies when the reconstituted wafer product is bonded with the one or more logic elements.

42. The product of claim 1 wherein either the first wafer, the second wafer, or both the first wafer and the second wafer are silicon wafers bonded to the dies containing diamond by either laser assisted heating, flash lamp heating, or both.

43. The product of claim 42 wherein the product further comprises a heat source absorption layer located at the bond interface wherein the heat source absorption layer contains at least one of the following elements: silicon, germanium, aluminum, tin, copper, silver, or gold.

44. The product of claim 1 wherein either the first wafer, the second wafer, or both the first wafer and the second wafer are silicon wafers bonded to the dies containing diamond by excimer laser heating.

45. The product of claim 1 wherein either the first wafer, the second wafer, or both the first wafer and the second wafer are silicon wafers bonded to the dies containing diamond by QCW or CW laser heating.

46. The product of claim 1, wherein one or both wafers are silicon wafers, and where the crystal orientation of one or both silicon wafers is either (100), (111), or (110), and the silicon originates from either the Czochralski (CZ) method or the Float Zone (FZ) method.

47. A reconstituted wafer product, comprising: a plurality of dies containing diamond attached to a first wafer in a manner that provides a thermally conductive connection between the first wafer and the dies containing diamond, and wherein the first wafer is a silicon wafer bonded to the plurality of dies containing diamond in areas that include one or more areas of recrystallized silicon.

48. The product of claim 47, wherein the one or more areas of recrystallized silicon are formed by excimer lasers.

49. The product of claim 47, wherein the one or more areas of recrystallized silicon are formed by QCW or CW lasers.

50. The product of claim 48, wherein the one or more areas of recrystallized silicon are formed by one or more heat sources and the one or more heat sources are heat sources on a die containing diamond level.

51. The product of claim 47, wherein the one or more areas of recrystallized silicon are formed by one or more heat sources and the one or more heat sources are heat sources on a wafer level.

52. The product of claim 47, wherein one or both silicon wafers further comprise a heat source absorption layer at the bond interface with the dies containing diamond.

53. The product of claim 52, further comprising a thermally resistive layer between the wafer and the heat source absorption layer prior to bonding.

54. The product of claim 52, wherein the heat source absorption layer located at the bond interface contains at least one of the following elements: silicon, germanium, aluminum, tin, copper, silver, or gold.

55. The product of claim 47 further comprising a second wafer wherein the second wafer is attached to the plurality of dies containing diamond in a manner that provides a thermally conductive connection between the first wafer, the dies containing diamond and the second wafer.

56. The product of claim 55 wherein the second wafer is a silicon wafer bonded to the plurality of dies containing diamond in areas that include one or more areas of recrystallized silicon.

57. The product of claim 1 wherein either the first wafer, the second wafer, or both the first wafer and the second wafer are silicon wafers bonded to the dies containing diamond by surface melting at the interface of the first wafer, the second wafer or both the first wafer and the second wafer with the dies containing diamond.

58. The product of claim 57 wherein the dies containing diamond each have a mean surface roughness on at least one side of at least 2 nanometers.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0006] FIG. 1 is a side cut-away view of diamond dies sandwiched between a first and second wafer with a gap filler material according to an aspect of the present disclosure.

[0007] FIG. 2 is a side cut-away view of diamond dies sandwiched between a first and second wafer with smoothening layers on the diamond dies according to an aspect of the present disclosure.

[0008] FIG. 3 is a side cut-away view of diamond dies coupled to a first wafer according to an aspect of the present disclosure.

[0009] FIG. 4 is a top-down cut-away view of a reconstituted wafer according to an aspect of the present disclosure.

[0010] FIG. 5 is a top-down cut-away view of a reconstituted wafer with a through-hole wafer gap filler according to an aspect of the present disclosure.

[0011] FIG. 6 is a side cut-away view showing a method for making a reconstituted wafer product with a through hole gap filler wafer according to an aspect of the present disclosure.

[0012] FIG. 7 depicts a side cut-away view of a reconstituted wafer with polished diamond dies on a carrier such as a tape in frame according to an aspect of the present disclosure.

[0013] FIG. 8 depicts a tape on reel delivery of diamond dies with cover tape according to aspects of the present disclosure.

[0014] FIG. 9 depicts another implementation of a reconstituted wafer without gap filler according to aspects of the present disclosure.

[0015] FIG. 10 shows a reconstituted wafer heat spreader product incorporated into a Chip on Wafer on Substrate (CoWoS) system stack according to an aspect of the present disclosure.

[0016] FIG. 11 shows a graph of absorption coefficient and penetration depth as a function of photon energy.

[0017] FIG. 12A is a side cut-away view of diamond dies sandwiched between a first and second wafer wherein each of the diamond dies are bonded in a deep pocket of the first wafer (logic side wafer).

[0018] FIG. 12B is a side cut-away view of diamond dies sandwiched between a first and second wafer wherein each of the diamond dies are bonded in a deep pocket of the second wafer (heatsink side wafer).

[0019] FIG. 12C is a side cut-away view of diamond dies sandwiched between a first and second wafer wherein the diamond dies are bonded in a shared shallow pocket of the second wafer (heatsink side wafer).

[0020] FIG. 12D is a side cut-away view of diamond dies sandwiched between a first and second wafer wherein each of the diamond dies are bonded in individual pockets in both the first wafer and the second wafer.

[0021] FIG. 12E is a side cut-away view of diamond dies sandwiched between a first and second wafer wherein each of the diamond dies are bonded in a shared pocket in both the first wafer and the second wafer.

DETAILED DESCRIPTION

Introduction

[0022] It is often prohibitively expensive or impractical to fabricate an SCD wafer or polycrystalline diamond (PCD) wafer of certain standard semiconductor wafer diameters, such as 300 mm or 450 mm, with semiconductor surface specifications. According to aspects of the present disclosure, it would be desirable to produce a reconstituted wafer having an array of diamond (e.g. SCD or PCD) dies or diamond die stacks that can be shipped to a semiconductor device fabrication plant (sometimes called a fab or foundry) in a configuration that is compatible with semiconductor processing done by the plant. As used herein, a reconstituted wafer refers to a wafer where multiple diamond (e.g. SCD or PCD) dies are placed on a temporary or permanent carrier wafer. There are a number of technical challenges to configuring and fabricating such a reconstituted wafer.

[0023] One challenge is to make the diamond die surface smooth enough for bonding and to make the diamond die thickness tolerance tight enough for bonding. In some implementations a smoothening layer or compliant layer may be used between the diamond die and the layers above and/or below it to ensure the desired smoothness and/or thickness tolerance.

[0024] Another challenge is that the surface of the diamond die or smoothening material may be incompatible with typical semiconductor fabrication processes. To address such challenges, in some implementations a wafer, e.g., a silicon wafer, may be bonded to the logic-facing surface of the diamond dies or die stacks and thinned, e.g., to <100 m or <10 m. The resulting stack may be easily bonded to a semiconductor wafer on which logic elements are formed. Making the wafer that is bonded to the diamond very thin adds little thermal resistance to the overall diamond die stack.

[0025] Yet another challenge is that the diamond dies or die stacks are typically placed on an underlying wafer (sometimes called a carrier wafer) with gaps between adjacent dies. Such gaps may present challenges during subsequent processing steps. For example, the gaps may lead to structural support issues if the diamond dies or die stacks are covered by a layer of material that is thinner than the width of the gaps. Furthermore, the gaps may present problems of edge rounding during subsequent surface finishing steps, e.g. during chemical mechanical polishing (CMP). Additionally, the gaps may trap contaminants that are hard to remove. To address such challenges, the gaps may be filled with appropriate gap-filling materials.

[0026] It has further been realized that there is a need for a fabrication method for reconstituted diamond wafers with low thermal resistance, while simultaneously minimizing reconstituted wafer warpage, damage, and thermomechanical stress due to excessive thermal budgets during fabrication. As such, there is a need for a low-temperature reconstituted wafer fabrication method while ensuring low thermal resistance. Extremely high-force copper-to-copper thermocompression bonding (TCB) is typically not considered with IC logic wafers, yet suitable for passive stacks like the reconstituted wafer. The compressibility (malleability) of metals (especially after annealing to soften the metals) make metals the perfect low thermal resistance bond material for extremely high force, yet low temperature, bonding, but IC logic is susceptible to stress induced breakage and damage and therefore extremely high force bonding is not typically used in fabrication of fragile parts in IC related products, e.g. ultrathin IC wafers The benefits of extremely high force metal bonding are minimizing voids around particles, ensuring improved bonding to diamond die edges despite CMP roll-off of metal films (e.g. copper) on diamond dies, reduced need of CMP due to improved compatibility with rougher surfaces, reduced sensitivity to metal oxides impeding metal interdiffusion, and bonding at lower temperatures avoiding excessive thermal stress due to CTE mismatch between high CTE metals and low CTE silicon and diamond. As a rule of thumb, high-force thermocompression bonding (TCB) allows for high thermal conductivity (low thermal resistance) bonds when using high purity single-element metals (e.g. copper, silver, gold, aluminum), whereas low-force bonding often results in deterioration of thermal conductivity of the bond, due to the use of multinary metals or compounds, e.g. multinary metals like solder, eutectics, transient liquid phase bond materials, or bonding with amorphous or polycrystalline materials. As an example, porous, low-k dielectrics in BEOL of IC wafers may be more vulnerable to damage due to bond force (pressure), and the gaps (pores) may reduce its mechanical properties by 50%, thereby reducing the damage threshold to e.g. below 50 MPa limit. Furthermore, strain engineering to enhance performance of transistors in CMOS is sensitive to externally applied stress. This lower damage threshold for IC wafers may not exist when bonding diamond by high-force metal bonding to silicon wafers into a reconstituted wafer thus aspects of the present disclosure may implement high force bonding techniques with the diamond dies and silicon wafers which were previously considered too damaging to use on IC related devices.

[0027] According to aspects of the present disclosure, a large diameter (e.g., 300 mm diameter) product may be shipped to a fab as a reconstituted wafer, having diamond dies in various forms (e.g., with or without filler, with or without a smoothening layer, with or without a compliant layer) temporarily or permanently bonded to one or two wafers, e.g., single crystal silicon (sc-Si). One or both wafers may be thinned prior to shipping the reconstituted wafer to the foundry (fab), and/or thinned at the foundry (fab). Additionally, having an ultrathin silicon wafer (e.g. 10 m or thinner) sandwiched between the diamond dies and the logic elements adds very minimal thermal resistance to the overall device stack. Similarly, the roughness of the diamond die does not negatively impact the performance of the reconstituted wafer heat spreader product. Shipping a 300 mm product helps with integration in a semiconductor 300 mm foundry (e.g. cleaning, thin film deposition, CMP, bonding), since these fabs typically have the infrastructure and experience to deal with 300 mm wafers but might not have infrastructure and experience to deal with diamond dies.

[0028] As shown in FIG. 1 one or more dies containing diamond 101, hereinafter diamond dies, may be sandwiched between a first wafer 102 and second wafer 104 to form a reconstituted wafer 100. In the implementation shown an array of diamond dies having rough top and bottom surfaces may be coated with an adhesion layer. Adhesion layer materials include, for example and without limitation, Titanium, Titanium-carbide, Chromium, and Chromium-Carbide. In some alternative implementations the adhesion layer may be omitted. For example, and without limitation, a smoothening layer such as silicon (e.g., polycrystalline or amorphous) may not require the adhesion layer to be deposited on and may form strong bonds with the diamond dies. The diamond dies 101 are arranged close together and their rough logic-side surfaces are coated with a continuous smoothening layer 108A. Here the smoothening layer partially fills gaps between each of the diamond dies creating a smoothened diamond die assembly. The resulting smoothened diamond die assembly is bonded to the first wafer 102 by a logic-side diamond bond material 110A; here the first wafer is the logic side wafer, which means that this wafer may be attached to another semiconductor wafer (not shown) on which integrated circuits are formed or will be formed. The second wafer 104 is referred to herein as the heat sink side wafer, which means that this wafer may be attached to a heatsink, or a wafer on which a heat sink is or will be formed, or a temporary wafer that will be removed prior to introducing the heat sink.

[0029] The diamond dies 101, or dies containing diamond, may be single-crystal diamond (SCD), polycrystalline diamond (PCD), or composites of diamond with metals, e.g. a mixture of diamond and copper, or a mixture of diamond and silver, or a mixture of diamond and silicon carbide, or a mixture of diamond and silicon. A mixture might mean a random 3-dimensional distribution of one material in the other material. A mixture might mean an organized 3-dimensional structure of one material in the other material. A mixture might mean a combination of a random and organized distribution of one material in the other material. Similarly, diamond dies may be stacks of diamond with copper, or diamond with silicon carbide, or diamond with silicon, or diamond with aluminum. The diamond dies 101 may be stacks that incorporate adhesion layers, diffusion barriers, smoothening layers, bond layers 110, 110A, 110B, filler materials for height matching in advanced chip packages, or precursors to bond line materials. As used herein the terms diamond die and dies containing diamond may be used interchangeably. In addition to the diamond dies, dummy dies may be placed in the reconstituted wafer product 100 at locations corresponding to the location of logic elements that are not known good dies. This results in a reconstituted wafer product with diamond dies located at the position of known good dies, and dummy dies at the location of logic elements that are not known good dies. Dummy dies may be made out of any suitable thermally conductive material for example and without limitation, silicon. Additionally in some implementations, for stability, dummy dies may be placed in locations in the reconstituted wafer corresponding to empty spaces between the attached logic elements and/or locations that promote structural stability of the reconstituted wafer product. Composites of diamonds may be with copper, silver, gold, aluminum, or zinc.

[0030] The thermal resistance of the reconstituted wafer product 100 from the logic side to the heatsink side when integrated into the final chip package may be less than 2000 m.sup.2-K/GW (2 mm.sup.2-K/W), more preferably less than 1000 m.sup.2-K/GW (1 mm.sup.2-K/W), even more preferred less than 500 m.sup.2-K/GW (0.5 mm.sup.2-K/W). It should be noted that the thermal resistance for the shipped product may be higher, since the wafer on the logic side and/or the wafer on the heat sink side may be thinned at the customer (foundry) site prior to or after bonding to the logic elements. Alternatively, the shipped product may contain a temporary carrier with a temporary adhesive that may be removed at the foundry.

[0031] The thermal resistance of the wafers, adhesion layers, diffusion barrier layers, bond layers, smoothening layers, compliant layers, metal foils, filler materials, diamond dies, or other materials that may be used in the reconstituted wafer product and that may be in the path of heat transport may be designed and/or treated to reduce the thermal resistance. Thermal resistance may be reduced by reducing the thickness of the layer. Thermal resistance may be reduced by increasing the thermal conductivity of the layer, e.g., by selecting higher thermal conductivity materials. Thermal conductivity may be enhanced in each layer by selecting higher purity materials. Thermal conductivity may be enhanced by reducing crystal defects, e.g., vacancies, or interstitials, e.g., by annealing. Thermal conductivity may be enhanced by reducing the number of grain boundaries, e.g., by optimized deposition conditions, or by post-deposition treatments, e.g. laser annealing. Thermal conductivity may be enhanced by making the material more isotopically pure, e.g. by using isotopically enriched deposition materials. The directionality of the thermal conductivity of the layer may be controlled by controlling the layer's crystal orientation, e.g. by selecting an optimized wafer crystal orientation, or by optimized deposition conditions. Thermal resistance may be reduced by optimizing the structure of the interface, e.g., the roughness. Thermal resistance may be reduced by optimizing both the thickness and the interface structures of the various layers in the product. Additionally, the thermal resistance may be reduced by increasing the overlap in the vibrational Density of States (DOS) of adjacent layers, or the vibrational spectra, e.g., by taking into account the sound velocity, Debye temperature, and elastic modulus of the layers.

[0032] The logic-side wafer 102 may contain silicon (e.g., single crystal silicon) and may be permanently bonded to diamond dies 101. The logic-side wafer may contain silicon (e.g. single crystal silicon) and may be temporarily bonded to the diamond dies. The logic-side wafer 102 may contain glass or sapphire or silicon carbide or polycrystalline diamond and may be temporarily bonded to the diamond dies 101.

[0033] By way of example, and not by way of limitation, the heatsink-side wafer 104 may contain silicon (e.g., single crystal silicon) and may be permanently bonded to diamond dies 101. The heatsink-side wafer 104 may contain silicon (e.g., single crystal silicon) and may be temporarily bonded to the diamond dies 101. The heatsink-side wafer 104 may contain glass or sapphire or silicon carbide or polycrystalline diamond and may be temporarily bonded to the diamond dies 101. The heatsink-side wafer 104 (e.g., single crystal silicon) may be attached to the diamond dies 101 via thick copper foil.

[0034] In other non-limiting example implementations, the reconstituted wafer product 100 may be a permanent stack of a single crystal silicon wafer on the logic side, diamond dies between both wafers, and a single crystal silicon wafer on the heat sink side. The reconstituted wafer product may be a permanent stack of a single crystal silicon wafer on the logic side, diamond dies with copper foil facing the heat sink side, and a single crystal silicon wafer on the heat sink side. The reconstituted wafer may be a stack of a permanently bonded single crystal silicon wafer on the logic side, diamond dies with copper foil facing the heat sink side, and a temporarily bonded wafer (carrier) on the heat sink side.

[0035] The reconstituted wafer product 100 may have alignment marks or fiducials to aid accurate alignment during bonding to the logic elements. The alignment marks may be on one or both of the outer surfaces of the reconstituted wafers. The alignment marks may be on one or both of the inner wafer surfaces of the reconstituted wafers.

[0036] During production the logic-side wafer 102 may act as a carrier having a thickness of greater than 100 micrometers (microns). Later, after assembly, the logic-side wafer may be thinned to less than 100 microns in thickness and in some implementations less than 10 microns in thickness. Before bonding the logic-side wafer 102 may be coated in a bonding layer 110A that is complementary to the smoothening material 108A. For example, and without limitation, if the smoothening material is copper then the bonding layer may also be copper such that the smoothening layer may be used with thermocompression bonding to bond copper on the wafer to copper on the diamond die.

[0037] In some implementations, according to aspects of the present disclosure, the locations of each of the diamond dies 101 may correspond to hot spots in logic elements of the targeted logic wafers. In some implementations, according to aspects of the present disclosure, the locations of each of the diamond dies 101 may correspond to the locations of the IC (e.g., logic) dies of the targeted IC (e.g., logic) wafer. In some implementations, according to aspects of the present disclosure, the locations of each of the diamond dies may correspond to the locations of the known good dies (KGD) of the targeted IC (e.g., logic) wafer. In some implementations, according to aspects of the present disclosure, the size of the diamond dies may correspond to the size of the IC (e.g. logic) die of the targeted IC (e.g., logic) wafer. In some implementations, according to aspects of the present disclosure, the size of the diamond dies may be slightly smaller than the size of the IC (e.g. logic) die of the targeted IC (e.g., logic) wafer. In some implementations, according to aspects of the present disclosure, the size of the diamond dies 101 may be slightly larger than the size of the IC (e.g., logic) die of the targeted IC (e.g., logic) wafer and partially or completely cover the dicing street width.

[0038] The gaps between adjacent diamond dies 101 are fully filled with a gap filling material 112. In some implementations the gap filling material may partially fill the gaps between the diamond dies instead of completely filling them. As a non-limiting example, the gap may only be filled near the logic side wafer, e.g., filling the gap up to a height of 100 micrometers. As discussed below the gap filling material 112 may be a raw or doped silica glass formed by methods such as spin on glass application. Alternatively in some implementations a through-hole wafer may be used as the gap filler, e.g. a single-crystal silicon through-hole wafer. Furthermore, the gap-filling material 112 may contain one or more of the following: a sol-gel, oxide powder, silicon powder, silicon carbide powder, copper paste or powder, silver paste or powder, graphite or carbon powder, solder, eutectic, brazing material, transient liquid phase precursors mixture, polymer, thermoplastic, curable adhesive (e.g., thermal, optical, or moisture curable), molding compound, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, spin-on glass, polymer-derived ceramics, silicones, polybenzimidazole, or polyimides. In some implementations the gaps may be partially or completely filled by a powder, e.g. silicon powder, and subsequently the powder may be sintered or melted to a (porous) solid, e.g. by laser annealing. In some alternative implementations the gaps may be partially or completely filled by sintering, e.g., copper or silver sintering. Alternatively, the gaps may be partially or completely filled by a copper nanopowder followed by a flash lamp anneal, e.g., PulseForge. In yet other implementations the gaps may be partially or completely filled with a composite of silicon powder and sol-gel. In yet other alternative implementations, the gaps may be partially or completely filled with a composite of silicon powder and a curable adhesive. Alternatively, the gaps may be partially or completely filled with a composite of silicon powder and a thermoplastic. In yet other alternatives the gaps may be partially or completely filled with a composite of a curable adhesive and carbon powder. In some implementations the powder is part of a formulation that includes additives to control stability, e.g., surfactants, and application, e.g., rheology modifiers. A non-exhaustive list of additive examples includes binders, anti-settling agents, dispersants, curing agents, anti-foaming agents, and thinners (e.g., solvents). In some preferable implementations, the gap filler is compatible with conventional silicon IC wafer dicing, e.g., the gap filler contains silicon. In some implementations, the gaps may be filled by one method, yet in other embodiments, the gaps may be filled by two or more methods of the above-described alternative methods. The two or more methods may be used sequentially inside the same gaps, or the two or more methods may be used at different locations, e.g., near the wafer center and near the wafer perimeter.

[0039] A second smoothening layer 108B may be disposed on top of diamond dies 101 and the gap filling material 112. The second smoothening layer herein may be referred to as the heatsink side smoothening layer. A second wafer 104 referred to as the heatsink-side wafer may be coated with a heatsink-side diamond bond material 110B that is compatible with the heatsink-side smoothening layer 108B. Thus, a reconstituted wafer product may be created having diamond dies sandwich between two wafers. This implementation creates a packaged diamond die product that is resistant to breakage and provides for ease of integration in other products.

[0040] FIG. 2 depicts an alternative implementation of the diamond die package shown in FIG. 1. In this implementation each of the diamond dies 101 is individually coated with a smoothening material 108A. Subsequently each of the diamond dies may be bonded individually with the logic-side diamond bond layer 110A on the logic side wafer 102. As a result, the gap filler material 112 may be deposited in gaps in the smoothening layer 108A between the diamond dies as well as the gaps between each of the diamond dies 101. Additionally, in implementations that use a through-hole wafer gap filler 112 the height of the wafer may be selected to accommodate the height of the diamond dies with the smoothening layer. This implementation may make it easier to accurately place the diamond dies onto the logic side wafer.

[0041] In some implementations, such as those discussed below with respect to FIG. 6, the diamond dies 101 may be inserted into corresponding openings in a through-hole wafer. The material of the through-hole wafer between the openings acts as a gap filler material 112. The diamond dies and through-hole gap filler assembly may be coated in a smoothening layer after the dies have been inserted into the through-holes.

[0042] In some implementations, without limitation, diamond dies may be first coated on one or both sides with a smoothening material, e.g., copper, followed by an optional smoothening of one or both top and bottom surfaces, e.g., with CMP, followed by bonding to one of the wafers, e.g., the logic-side wafer 102, followed by depositing an optional gap filler 112 and optional planarization of the gap filler, followed by deposition of an optional global smoothening layer 108B (in contrast to a local smoothening layer on each diamond die), followed by an optional smoothening of the global smoothening layer, followed by bonding to an optional second wafer, e.g., the heat sink side wafer 104.

[0043] In some implementations, without limitation, diamond dies may first be temporarily placed on a temporary carrier, followed by deposition of a gap filler and an optional planarization of the gap filler, coated globally with a smoothening material, e.g. copper, followed by an optional smoothening of the global smoothening material, e.g. with CMP, followed by bonding to one of the wafers, e.g. the logic side wafer, followed by removing the temporary carrier, followed by deposition of a global smoothening layer, followed by an optional smoothening of the global smoothening layer, followed by bonding to an optional second wafer, e.g. the heat sink side wafer.

[0044] FIG. 3 depicts another alternative implementation of a reconstituted diamond dies wafer 300 according to aspects of the present disclosure. In this implementation the logic side wafer is omitted as compared to FIG. 1. Instead, a bonding layer 110 is directly deposited on the logic-side smoothening layer 108A. This bond layer bonds the reconstituted wafer directly to logic elements (not shown). The material of the bonding layer 110 is chosen to be compatible for bonding methods to the IC wafer as discussed in the bond sections.

[0045] The diamond dies may be sunk into the logic side wafer into blind holes bonded in silicon wafers as depicted in FIGS. 12A-12E. Blind holes referred to herein as pockets may be manufactured on the side facing the diamond die 1201 in the logic-side wafer 1202 as shown in FIG. 12A, on the side facing the diamond die 1201 in the heatsink side wafer 1204 as shown in FIG. 12B, or in both wafers as shown in FIG. 12D. The pockets may be below 10 micrometers deep, but more preferably over 100 micrometers deep, or even more preferred of similar depth as the diamond die thickness (greater than 90 percent of the thickness of the diamond die within the blind hole is referred to herein as a deep pocket), or roughly half the diamond die thickness in case of two pocketed wafers, or there may be many different pocket depths distributed over the total diamond die thickness in case of two pocketed wafers. In the example implementation shown in FIGS. 12C and 12E the diamond dies 1201 may be sunk into a shared pocket, that is, multiple diamond dies 1201 may be bonded to a wafer (either logic side or heatsink side or both) inside a single blind hole. Additionally, as depicted in FIG. 12C the diamond die may be partially sunk into one of the wafers in what is referred to herein as a shallow pocket which covers less than 90% of the diamond die. The other wafer may be a flat wafer bonded with a smoothening layer and bond layer similar to as discussed above or may be another wafer with a shallow pocket and the wafers 1202, 1204 bonded at an interface 1215 as shown in FIGS. 12D and 12E. As depicted in FIGS. 12A-12E the bond region or regions 1210A, 1210B may be pockets in the wafer and may also include a bonding material. Alternatively, the bonding region or regions may be pockets of molten silicon that subsequently are recrystallized after the diamond die 1201 are sunk into them and bonded as will be discussed.

[0046] In some implementations a copper foil may be present between the diamond die and the silicon wafer, the pocket depths may be adjusted to accommodate the sum of the diamond die and copper foil thickness. Alternatively, instead of copper foil, aluminum foil, or SiC may be used. As such, the silicon side walls of the pockets fill the gaps between the diamond dies of the reconstituted wafer. These gaps can be 100 micrometers wide or even a few 100 micrometers wide. The width of these gaps may be largely dictated by the wafer map and dicing process details related to the IC (e.g. logic) wafer. These silicon walls may provide mechanical support to the final reconstituted wafer, especially after thinning one or both of the wafers. Additionally, these walls may be in the path of dicing where the dicing equipment and process may be mostly designed to dice through silicon or silicon IC wafers. The pockets may be slightly larger in lateral dimensions than the diamond die to ensure ease of placement inside the pockets, e.g. 10 micrometers, preferably less than 5 micrometers, even more preferably less than 2 micrometers larger than the diamond die. The pockets, e.g. corners or sidewalls, may be used in conjunction with cameras to enhance placement accuracy of the diamond dies. Additionally, the pockets may be used as alignment marks to align the reconstituted wafer with the IC (e.g. logic) wafer. The bonding material (e.g. copper foil, aluminum foil, etc.) may fill the entire pocket after bonding or may be located in a portion of the pocket for example and without limitation, the bottom of the pocket.

[0047] The pockets may be created in the bulk material of the wafer, e.g., silicon. Alternatively, these pockets may be created in a top layer containing at least one of the following: silicon, germanium, aluminum, tin, copper, silver, gold, zinc, silicon carbide, silicon oxide, a sol-gel, polymer, thermoplastic, curable adhesive, molding compound, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, spin-on glass, polymer-derived ceramics, silicones, or polyimides. For example, and without limitation, a metal foil may be attached to the wafer, and subsequently pockets are created inside the metal foil, e.g., copper foil, or aluminum foil. The metal foils may be annealed to reduce hardness and tensile strength, and increase ductility, and make the foil softer. In yet another example, a metal layer is deposited onto the wafer, e.g., by plating, and the pockets are created in the deposited layer. The pockets may be created by removing material from the bulk wafer or the top layer, or the pockets may be created by additive manufacturing.

[0048] These pockets may be created by removing silicon by mechanical means, e.g., by computer numerical control (CNC) machining, or by optical means, e.g., by laser ablation. Alternatively, these pockets may be created by photolithography and etching. Etching may be performed by wet or dry etching. A hard mask may be formed prior to etching. Wet etching may be isotropic, yet preferably anisotropic. The most common isotropic etchants are a combination of hydrofluoric acid, nitric acid, and acetic acid (HNA); the most common anisotropic etchants are potassium hydroxide (KOH), ethylenediamine pyrocatechol (EDP), and tetramethylammonium hydroxide (TMAH). The wet etching agents may be sprayed onto a rotating wafer. The reaction rate may be roughly 10 micrometers of silicon removal per minute. Alternatively, electrochemical etching may be used. Dry etching may be performed by reactive ion etching (RIE), deep reactive ion etching (DRIE, e.g., the Bosch process), inductively coupled plasma (ICP) etching, or electron cyclotron resonance etching (ECR), typically with fluorine-based gasses. RIE, DRIE, ECR, and ICP are preferred due to their anisotropic nature. Alternatively, plasma etching is used, albeit less preferred due to its isotropic nature. Other dry etching methods that may be used are ion beam etching (IBE), cryogenic RIE, high-density plasma (HDP) etching, atmospheric downstream plasma dry chemical etching (ADP DCE), microwave plasma etching, or electron enhanced material processing (EEMP). Alternatively, these pockets may be created by a combination of two or more of the above methods.

[0049] The silicon may be resistive, lightly doped, or heavily doped, albeit preferably not heavily doped. The silicon may originate from silicon ingots grown by the Czochralski (CZ) method or the Float Zone (FZ) method. Furthermore, the silicon may have a typical orientation of (100), (111), or (110). The (100) orientation may be preferred for anisotropic wet etching and is most readily available. The (111) orientation may be preferred for mechanical stability after thinning. The (110) may be preferred for the combination of mechanical stability, smoothness, and anisotropic etch ratio. The silicon may have a preferred crystal orientation that promotes bonding by e.g. promoting the preferred crystal orientation of the bond layers, e.g. by promoting a preferred crystal orientation of the seed layer prior to plating, e.g. to form nanotwinned (111) oriented copper bond layers. The silicon thickness may be a standard thickness, e.g. 775 m thickness for 300 mm diameter wafers. Alternatively, the silicon thickness may deviate from the standard thickness to accommodate both the height necessary for the pockets, and additional thickness for ease of handling during the manufacturing process of the reconstituted wafers. Additionally, methods may be used to reduce wafer-edge defects to ensure high yield bonding to the IC (e.g. logic) wafers. These include techniques involving both wet and dry etching at the wafer edge, chemical mechanical polishing (CMP), edge deposition, and edge trimming steps. The silicon wafer may be a silicon-on-insulator (SOI) wafer. The silicon wafer may have an epitaxial film on the diamond side.

[0050] In addition to the pockets, simultaneously or sequentially, via the same or similar processes, alignment marks may be created on one or both wafers to improve alignment with the IC (e.g., logic) wafer prior to or during the bonding process. The alignment marks may be located outside the diamond dies areas, e.g., near the perimeter.

[0051] The diamond dies may be bonded into the pockets by copper-to-copper bonding, e.g., by copper-to-copper thermocompression bonding (TCB), or copper-to-copper plasma-assisted bonding (PAB), or copper-to-copper surface activated bonding (SAB), or copper-to-copper atomic diffusion bonding (ADB), or copper-to-copper ultrasonic bonding, or by silver-to-silver bonding, e.g., silver-to-silver TCB, SAB or ADB, or by gold-to-gold bonding, e.g., gold-to-gold TCB, SAB, or ADB, or by aluminum-to-aluminum bonding, e.g., aluminum-to-aluminum TCB, SAB, or ADB. TCB may be referred to as solid-solid (inter) diffusion bonding or direct solid-state diffusion bonding. The bond temperature may be reduced by increasing bond force where more force reduces the need for temperature driven atomic diffusion. In some implementations the bond temperature may be reduced to 150 Celsius by passivation layers or cap layers, e.g., gold, on reactive metals like copper. Additionally, the bond temperature may be reduced by plasma passivation, e.g., by atmospheric plasma passivation with nitrogen or hydrogen. In other implementations the bond temperature may be reduced to 150 Celsius when the surface oxide, e.g., copper oxide, is removed prior to bonding, removal of the surface oxide may be performed by one or more of the following methods: wet treatment, e.g., acid treatment like citric acid treatment, dry treatment, e.g., forming gas treatment, or plasma treatment, or ion beam treatment, or vacuum plasma treatment, or atmospheric plasma treatment, etc. In yet other alternatives the bond temperature may be reduced by in-situ cleaning, e.g., oxide removal, and subsequent handling in inert environments prior to bonding, e.g., to minimize surface oxide reformation. The bond temperature may also be reduced by use of self-assembled monolayers (SAM) of alkane-thiols with the aim to protect the metal surface, e.g., copper, against excessive oxidation in metal-to-metal bonding. In some implementations, the bond temperature may be reduced to 150 Celsius by grain size and orientation control, e.g., by using nanotwinned (111) copper at the bond surface. The bond temperature may be reduced to room temperature by using SAB or ADB. In other implementations, the bond temperature may be reduced to 150 Celsius by use of ultrasonics. It should be understood that any of the above-described alternatives for reducing bonding temperature may also be used in combination with each other where compatible.

[0052] The diamond dies 1201 may be bonded into the pockets by silver sintering or copper sintering. Alternatively, the diamond dies may be bonded into the pockets by brazing, e.g., with Cu-ABA at 1025 Celsius. In yet other alternative implementations the diamond dies may be bonded into the pockets by eutectic bonding, e.g. the aluminum-silicon eutectic (e.g., 88.3Al/11.7Si by wt.-%) at bond temperatures of roughly 575 Celsius, or e.g., the aluminum-germanium eutectic (e.g., 55Ge/45Al by wt.-%) at bond temperatures of roughly 425 Celsius, or e.g. the zinc-aluminum eutectic (e.g. 95Zn/5Al by wt.-%) at bond temperatures of roughly 385 Celsius.

[0053] The diamond dies 1201 may be bonded into the pockets by transient liquid phase bonding (TLPB, also referred to as solid-liquid interdiffusion bonding or SLID bonding, or isothermal solidification), e.g., nickel-tin TLPB at bond temperatures of roughly 300 Celsius, or e.g. copper-tin TLPB at bond temperatures of roughly 280 Celsius, or e.g., silver-tin TLPB at bond temperatures of roughly 250 Celsius, or e.g. gold-indium TLPB at bond temperatures of roughly 200 Celsius, or e.g., silver-indium TLPB at bond temperatures of roughly 180 Celsius. TLPB (or SLID bonding) may be achieved by depositing films, e.g., by plating or PVD, of different compositions on each bonding surface, e.g., nickel on one surface, and tin on the other surface. Alternatively, by depositing nickel on both surfaces, and tin on one or both surfaces. Alternatively, TLPB may be achieved by using a paste containing a mixture of nano-sized or micron-sized powders of different compositions, e.g., a mixture of copper-based and tin-based powders. In yet another example, TLPB may be achieved by depositing one or more thin films, e.g., by plating or PVD, on one or both surfaces, in combination with a paste or a foil of a different composition, e.g., silver films in combination with an indium foil. Pastes may be applied by a multi-step process where after paste application, a heating step may be implemented prior to bonding to remove most or all of the volatiles, e.g., organics. TLPB may be based on binary systems, e.g., nickel-tin, copper-tin, gold-tin, silver-tin, copper-indium, gold-indium, silver-indium, copper-gallium, etc. or multinary systems, e.g., copper-bismuth-tin, copper-bismuth-indium, copper-indium-tin, etc. In some implementations, the bond temperature may be reduced by replacing indium with a mixture of indium and bismuth, e.g. the eutectic with a solid-to-liquid temperature of 109 Celsius. In some embodiments, other fusible alloys may be used, e.g., bismuth-containing eutectic fusible alloys, e.g. the eutectic bismuth-tin alloys (e.g., Bi58Sn42 by weight with eutectic temperature of 138 Celsius). Various bond techniques may be aided by ultrasonics, e.g. TLPB may be aided by ultrasonics to increase the shear strength, e.g. ultrasound-induced TLPB, solder bonding may be supported by ultrasonics, etc. TLPB may be performed above or below the melting point of the low-melting metal.

[0054] Bonding may involve a low temperature, e.g., below 100 Celsius, or room temperature, e.g. around 25 Celsius, pre-bonding step, e.g., a cold-welding step, prior to a subsequent high temperature, e.g. at or above 150 Celsius, bonding step, e.g., with force, and/or anneal step, e.g., without force. The cold welding may involve gold layers, e.g., gold cap layers on each surface. Alternatively, the cap layer may be silver, titanium, manganese, or palladium. In some implementations the grain size and grain orientation may be controlled to improve bond strength (e.g., nanotwinned (111) copper). Surface contaminants like oxides may be removed by wet and dry cleaning, e.g., a citric acid clean to remove surface copper oxides. In some implementations, surface contamination (e.g., oxides) may be removed by a plasma, a beam, a flux less vapor (e.g., formic acid vapor or anhydrous HF vapor) or atomic layer etch with halogens (e.g. HF, Cl.sub.2). In some implementations, the surface oxide may be removed by annealing prior to bonding, e.g., by vacuum annealing. In some implementations, the metal surface may be passivated by an atmospheric plasma (e.g., a helium (He) plasma containing nitrogen). The gold layer may be 25 to 100 nanometers thick. In general, noble metals may be used as a cap layer on more reactive metals, e.g., copper, to avoid reaction of the more reactive metal with the atmosphere, e.g., oxidation. A thin diffusion barrier, e.g., titanium, may be used in between the more reactive metal, e.g., copper, and the cap layer, e.g., gold. After pre-bonding, and final bonding, the cap layer may have diffused into the more reactive metal.

[0055] The diamond die may be bonded into the pockets by wafer surface melting, e.g., by laser assisted heating or laser assisted bonding (LAB), e.g. excimer laser heating, or Continuous-Wave (CW) laser heating. Lasers may be high powered, e.g. one kilowatt or higher. The lasers may be any suitable type of laser for example and without limitation, gas lasers (e.g. excimer, or CO.sub.2), fiber lasers, diode lasers, or pumped solid state lasers, e.g. diode-pumped solid-state lasers. Excimer laser heating may be by high-power (e.g. kW), 1-100 nanosecond pulse length, UV lasers. Excimer laser annealing is commonly used in the display industry to convert CVD-Si thin films on glass substrates deposited at low CVD temperature to high-performance polycrystalline silicon transistors. CW laser assisted bonding may be accomplished by high-power (e.g. kW), 10's millisecond pulse length, blue lasers. CW lasers may be green lasers. LAB may be by solid-state diode lasers, fiber lasers, or infrared (IR) lasers. LAB may be by lasers with microsecond pulse lengths. LAB may be by Quasi-CW (QCW) fiber lasers. LAB may be by high power CO.sub.2 lasers (e.g., 10.6 micrometers). The lasers may reach the bond interface through the diamond dies, e.g., in case of a laser absorbed by the bulk of the silicon wafer. The laser energy may reach the bond interface through the silicon wafer, e.g., for wavelengths not absorbed by the silicon bulk, yet absorbed by an absorption layer at the bond interface. The absorption layer may be an IR absorbing layer. The absorption layer may be a doped silicon layer or a crystallographically modified silicon layer. The absorption layer may contain germanium, silicon carbide, amorphous silicon, or black silicon. The absorption layer may be deposited onto the pocketed silicon wafer by physical vapor deposition (PVD), or the absorption layer may be deposited onto the pocketed wafer by screen printing, or jetting, and may contain nanosized silicon particles, or nanosized carbon particles, or nanosized silicon carbide particles. Bonding of diamond dies by wafer surface melting may be performed by excimer laser annealing, blue or green CW laser annealing, QCW fiber laser annealing, flash lamp annealing (flash lamp assisted bonding, or FLAB), laser spike annealing, or rapid thermal processing (RTP), depending on the melting point, thermal conductivity, and absorption characteristics of an optional absorption layer, e.g., an absorption layer with a lower melting point than silicon with the absorption layer containing germanium, aluminum, tin, copper, silver, or gold, potentially mixed with silicon.

[0056] Similarly, silicon on insulator wafers (SOI) may be used for bonding of diamond by wafer surface melting to further increase the temperature for the silicon on top of the oxide layer due to the thermal resistance of the oxide, prior to the oxide layer partially or completely getting disrupted or dissolved due to the excessive heat. The diamond dies bonding based on silicon surface melting may be performed in an inert or a forming-gas atmosphere (e.g., a mixture of hydrogen and nitrogen gas), e.g., an inert gas purged atmosphere (e.g., argon, or nitrogen), or a vacuum atmosphere. Controlled pressure to promote bonding may be applied to the interface during the diamond dies bonding based on silicon surface melting, e.g., incorporating appropriate optically transparent materials to exert that pressure, and adapting their mounting for that functionality. Optically transparent (may include beyond the visible spectrum range) materials may be, without limitation, silica, sapphire, diamond, or silicon carbide. Diamond die roughness may act as a diffuser, e.g., with a collimated beam, and may achieve sufficient power density and a sufficiently high temperature in an extended area, e.g., the entire area of a diamond die. To further control the temperature depth profile, a combination of two or more of the above heat sources may be applied simultaneously, or sequentially, e.g., a hybrid system with the use of a short (e.g., UV) and long (e.g., IR) wavelength heat source. Laser bonding may be aided by ultrasonics, e.g., ultrasonic-assisted laser bonding. Alternatively, the diamond dies may be bonded to one or both wafers without pockets by wafer surface melting, e.g., by laser assisted heating or laser assisted bonding (LAB), as described above. After LAB the diamond bond regions may contain recrystallized silicon thus leaving areas of recrystallized silicon underneath and (in some implementations) around the diamond dies. In some implementations, bonding by wafer surface melting is performed with diamond dies coated with thin films, e.g., a smoothening layer, or a thin film aiding in bonding. In some implementations, bonding by wafer surface melting is performed with heat absorption layers deposited onto the wafers, or both the diamond dies and wafers. In some implementations of bonding by wafer surface melting, the wafers have no pockets.

[0057] In some implementations, a smoothening layer on the rough diamond dies may be added, e.g., a thin silicon film (e.g., by CVD or PVD), optionally smoothened by CMP, optionally annealed to increase crystallinity and thermal conductivity, and in addition or instead of wafer surface melting, the thin film on the diamond dies may partially or completely melt and aid in bonding to the wafer. In some implementations, the smoothening layer on the diamond dies may be the heat source absorption layer and aid in the bonding to the wafer. In some implementations, the diamond dies are polished SCD dies with a heat source absorption layer aiding in bonding to the wafer. In some implementations the diamond dies may be polished with a surface roughness on at least one side of at least 2 nanometers or greater. In some implementations, the thin film on the diamond dies is a heat source absorption layer aiding in bonding to the wafer where the thin film, and optionally the wafer surface, may partially or completely melt under the influence of a heat source, e.g., laser assisted bonding (LAB) or flash lamp assisted bonding (FLAB), and the thin film contains silicon, germanium, copper, tin, aluminum, silver, or gold. In some implementations of bonding by wafer or diamond die surface melting, the wafers have pockets. In some implementations of bonding by wafer or diamond die surface melting, the wafers have no pockets.

[0058] Laser assisted annealing, rapid thermal annealing, flash lamp annealing, and similar heat sources may also be used to increase either the thermal conductivity or increase the bond strength, or both, for bonding diamond dies to wafers involving e.g., semiconductor bond or smoothening materials, metal-based bond or smoothening materials, or dielectric bond or smoothening materials.

[0059] Alternatively, the diamond dies may be bonded into the pockets by surface activated bonding (SAB), plasma assisted bonding (PAB), atomic diffusion bonding (ADB), solder bonding, ultrasonic bonding, thermosonic bonding, brazing, or adhesive bonding. PAB bond surfaces may be exposed to water or ammonia prior to bonding. Hydroxyl groups may be formed at the PAB bond surfaces prior to bonding, or amine groups may be formed at the PAB bond surfaces prior to bonding. Adhesive bonds may be created with e.g., SU-8 (negative photoresist). BCB (benzocyclobutene), a prepolymer of PDMS (polydimethylsiloxane), or a dry film resist, e.g., Ordyl dry film. Ordyl is a trademark of Elga Europe of Milan, Italy. Adhesives may be thermally cured at low temperatures, UV cured at low temperatures, or moisture-cured at low temperature. It should be understood that any of these listed types of bonding may also be used in combination, where compatible.

[0060] All bond surfaces, e.g., wafer, pocket, or diamond dies may be deposited by the necessary bonding materials, e.g., metallization for metal bonding, dielectrics for PAB or SAB. The deposited bond materials may include adhesion, diffusion barrier, and seed layers. All bond surfaces, e.g., diamond dies, may be deposited by the necessary smoothening materials, which may include adhesion, diffusion barrier, and seed layers. All bond surfaces may be deposited by compliant materials for bonding.

[0061] Heat sources during bonding may be global, e.g., on a wafer level, or local, e.g., on a diamond die level. Local heat sources may be used to minimize the overall thermal budget to the reconstituted wafer in order to minimize damage or warpage, and may be used to minimize thermomechanical stress. Local heat sources may be provided by lasers. Alternatively, local heat sources may be, e.g., resistive heaters, lamp heaters, or inductive heaters. In yet another example, local heat sources may be ultrasonic sources. Yet in other embodiments, local heat sources may be multi-layer thermally reactive stacks or foils that provide instantaneous or extremely rapid heating, e.g., nickel and aluminum multi-layered stacks or foils. When activated by a small pulse of local energy from electrical, optical or thermal sources, the stack or foil reacts exothermically to precisely deliver localized heat up to temperatures of 1500 C. in fractions (thousandths) of a second, and will melt surrounding materials, e.g., solder, eutectics, or TLPB materials. These multi-layer thermally reactive stacks or foils may also be referred to as reactive nano-multilayers, self-propagating exothermic reaction (SPER) bonding materials, integrated reactive multilayer systems (iRMS), or a class of pyrotechnic materials. Alternatively, nano-thermites may be used as a local heat source, an intimate mixture of an oxidizer and a reducing agent, e.g., a metal fuel like aluminum, and an oxidizer like copper oxide. A reactive multi-layer stack for self-propagating exothermic reaction bonding may be fabricated by vapor-depositing thousands of alternating nanoscale layers of Aluminum (Al) and Nickel (Ni), either as a stack onto the wafer or the diamond die, or as a separate foil. By way of example, and not by way of limitation, an AlNi multi-layer thermally reactive foil is sold commercially under the name NanoFoil by Indium Corporation of Clinton New York. Nanofoil is a registered trademark of Thermal Conductive Bonding, Inc. of Sacramento, California. Other foil compositions may be boron-titanium, aluminum-titanium, titanium-silicon, or aluminum-palladium. In addition to the energetic multi-layer material other materials may be included in the stack that specifically melt, comply with surfaces, and react with the wafers or diamond dies to be bonded, e.g. solder, eutectics, or materials used for TLPB.

[0062] The pocketed wafers 1202, 1204 may be bonded to each other via the pocket walls by the same or an alternative bonding process as used for the bonding of the diamond dies into the pockets. The same holds for the sealing of the outer perimeter of the reconstituted wafer.

[0063] FIG. 4 is a top-down cut-away view of a reconstituted wafer 400 according to an aspect of the present disclosure. In this implementation the diamond dies 101 are disposed on the surface of the logic-side wafer 102. For ease of visualization the heatsink-side wafer 104 has been made to appear semi-transparent. Each of the diamond dies 101 is attached to the logic-side wafer 102, as discussed above. Between each of the diamond dies a gap filling material 112 such as glass has been deposited or otherwise formed. While in this implementation the diamond dies 101 are arranged in a regular pattern on the logic-side wafer 102, aspects of this disclosure are not so limited. For example, and without limitation, the diamond dies 101 may be placed on the logic-side wafer 102 in locations corresponding to one or more hotspots of one or more logic elements which may be coupled to the logic side wafer.

[0064] FIG. 5 is a top-down view of a reconstituted wafer 500 similar to that shown in FIG. 4, but with a through-hole wafer gap filler 512 according to an aspect of the present disclosure. As the name suggests, the through-hole wafer gap filler includes holes 503 which are configured, e.g., sized and shaped, to accept diamond dies 501. The dimensions of the holes may be chosen to snugly fit the diamond dies. Alternatively, the dimensions of the diamond dies may be slightly smaller than that of the holes to provide enough clearance that the dies fit easily into the holes. An adhesive material or filler may be placed around diamond dies in the holes to further stabilize the diamond die and gap filler assembly. The through-hole gap filler wafer 512 may be a silicon wafer fabricated by CNC machining or laser machining.

[0065] FIG. 6 is a side cut-away view showing a method for making a reconstituted wafer product with a through hole gap filler wafer 512 according to an aspect of the present disclosure. In this implementation, a logic-side wafer 502 may be coated in a logic side diamond bond layer 510A which is compatible with bonding to the diamond smoothening layer 508A. Additionally, the logic-side diamond bond layer 510A may be compatible with bonding to the through-hole gap filler wafer 512. In some implementations the through-hole gap filler wafer may also be coated in smoothening material or bonding material compatible with bonding with the bonding layer 510A.

[0066] Next, according to some aspects of the present disclosure the through-hole gap filler wafer 512 may be bonded to the logic-side wafer 502 with the bond layer 510A. Alternatively, the through-hole gap filler wafer 512 may be bonded to the logic side wafer 502 after the diamond dies 501 have been bonded to the logic side wafer. Alternatively, the through-hole gap filler wafer 512 is not bonded, and may be removed (e.g., used repeatedly). The through-holes 503 of the gap filler wafer 512 may be fitted over the diamond dies 501 allowing the gap filler wafer to make contact and bond with the bond layer 510A of the logic-side wafer 502. The through-hole gap filler wafer 512 may be made from silicon, e.g., single crystal silicon, or ceramics, e.g., sapphire, or silicon carbide. The through-hole gap filler wafer 512 may be manufactured by removing material from a solid wafer, e.g., by electrical discharge machining, laser cutting, water jetting, or water-guided laser cutting.

[0067] As discussed above, the diamond dies 501 may have their logic-side bonding surfaces coated in a smoothening layer 508A. According to some aspects of the present disclosure an adhesion layer may be disposed on the diamond bonding surface prior to the creation of the smoothening layer to improve adhesion of the smoothening layer with the diamond die. Shown here the bottom of the diamond die 501 is the bonding surface for the logic side and may be rough. The smoothening material 508A may fill and even out the rough surface making it suitable for bonding. More commonly, the smoothening material is smoothened after deposition, e.g., by polishing or grinding. The diamond dies 501 may then be fitted into the through-holes 503 of the gap filler wafer 512, e.g., after placing the through-hole gap filler wafer onto the bond layer of the logic-side wafer 502. Sufficient pressure and heat may be applied to the diamond dies 501 to bond to the logic-side wafer 502 with the bond layer 510A along with the through-hole gap filler wafer 512 according to the selected compatible bonding method as will be discussed in the bond sections. Alternatively, the diamond dies 510 may be fit into the through-holes 503 of the gap filler wafer 512 with the through-hole gap filler wafer on a temporary carrier. The smoothening layer 508A may then be applied to the resulting diamond die and gap filler wafer assembly. The assembly may then be bonded to the logic-side wafer 502 with the logic-side bond layer 510A. In some implementations after bonding the diamond dies 501 to the logic-side wafer 502, the logic side wafer may be thinned to less than 10 or less than 100 microns in thickness. A temporary carrier may be adhered to the logic side wafer to improve stability for subsequent process steps. The temporary carrier may be removed after completion of the product.

[0068] After the diamond dies and gap filler wafer are bonded to the logic side wafer, a smoothening layer 508B may be applied to the heatsink-side bonding surface of diamond dies 501 (shown here as the top) and the through-hole gap filler wafer 512. Alternatively, the smoothening layer 508B may be applied to the heatsink side of the diamond die 501 prior to placement of the diamond dies in the through-holes 503 of the gap filler wafer 512. In such cases the through-hole gap filler wafer may be bonded to the heatsink-side wafer 504 without the smoothening layer 508B.

[0069] Prior to bonding with the diamond die and through-hole gap filler wafer assembly, the heatsink-side wafer 504 may have a heatsink-side diamond bond layer 510B applied to the diamond bonding side of the wafer. The heatsink-side wafer diamond bond layer may be a material that is compatible with bonding to the smoothening layer 508B and, in some implementations, the bare gap filler wafer 512. After application of the bond layer, the heatsink-side wafer 504 with bond layer may be attached to the diamond die and gap filler wafer assembly by application of sufficient pressure and heat according to the selected compatible bonding method as will be discussed in the bond sections.

[0070] In some alternative implementations the diamond dies which are coated with a smoothening material may be bonded to the heat sink side wafer and the gap filler wafer may be bonded to the logic side wafer. The heatsink-side wafer and diamond die assembly may then have the diamond die porting inserted into the through-holes of the gap filler wafer on the logic side wafer and sufficient bonding pressure and heat applied to attach the two assemblies according to the chosen bonding method as discussed in the bond sections. Thus, may be created a reconstituted wafer product with a through hole gap filler wafer.

[0071] Dicing of the bonded pair of the IC (e.g., logic) wafer to the reconstituted diamond wafer may happen after bonding. Dicing of the bonded pair may be based on stealth dicing, plasma dicing, laser dicing, or saw dicing, or a combination. Dicing may happen in one step, or multiple steps, e.g., first dicing through the IC wafer from one side, and subsequently dicing the reconstituted diamond wafer from the opposite side. Dicing through the full thickness of, e.g., the heatsink-side wafer 504, may happen in steps, e.g., by adding grooves or cracks into the wafer prior to assembling the reconstituted wafer, or prior to bonding the reconstituted wafer to the IC (e.g., logic) wafer. Similarly, thinning of the heatsink-side wafer 504 may happen prior to bonding to the IC (e.g., logic) wafer, or after bonding to the IC (e.g., logic) wafer.

[0072] Additionally, some implementations may require less packaging for the diamond dies. For example and without limitation, the diamond dies may be packaged bare on tape on reel or tape on frame assemblies. The diamond surfaces may be polished, or rough. The diamonds may be coated with a smoothening layer on top and/or bottom side. The smoothening layer may have been smoothened by polishing. The heat sink side of the diamond may be bonded to thick copper foil. The copper foil may be coated with silicon or bonded to silicon. The diamonds may be coated by the precursor to a thermally conductive, compliant material for bonding, e.g. a solder, eutectic, or the precursor to transient liquid phase bonding (TLPB).

[0073] FIG. 7 depicts a side cut-away view of a reconstituted wafer 700 having polished diamond dies 701 on a carrier 702 such as a tape in frame or film frame according to an aspect of the present disclosure. In the implementation shown, the diamond dies 701 may be polished (for example less than 5 nanometers (nm) average surface roughness and less than 5 microns thickness variation) for ease of use. Alternatively, the diamond dies 701 may have an unfinished roughness from production (for example and without limitation, between 100 nm and 300 nm average surface roughness and a thickness variation of between 5 microns and 30 microns), or a lapped finish (for example between 5 nm and 100 nm average surface roughness and less than 5 microns of thickness variation). An adhesive layer 710 may be applied to the carrier 702. The polished diamond dies 701 may then be attached to the carrier with the adhesive layer 710. The carrier here may be flexible tape made from a material such as polyolefins, PVC, polyurethanes, or UV-curable tapes for film frame (tape in frame). Alternatively, the carrier 702 may be a rigid material for example and without limitation, a temporary semiconductor or glass wafer. The adhesive layer 710 may be a layer of temporary adhesive such as for example and without limitation a UV curing adhesive tape or a solvent curing adhesive, or pressure sensitive adhesive, or a thermoplastic material. The temporary adhesive such as UV cure adhesive may provide for easy removal of the diamond die from the carrier by exposure of the adhesive to the curing agent e.g. UV radiation of the appropriate wavelength. Alternatively, a permanent adhesive may be used and in which case the permanent adhesive and carrier would have to be removed by destructive methods such as grinding and/or polishing.

[0074] FIG. 8 depicts a tape on reel delivery of diamond dies 801 with cover tape 804 according to aspects of the present disclosure. As shown in this implementation the carrier substrate 802 includes multiple cavities 803 for diamond dies. The diamond dies 801 may be inserted into the cavities 803 and then covered with the cover tape 804. The carrier substrate 802 may be made from a flexible material for example and without limitation paper, or a plastic such as polycarbonate or polystyrene. Similarly, the cover tape may be made from a flexible material suitable for covering the diamond dies and attaching to dividers of the carrier. The cover tape may be made from for example and without limitation a heat activated plastic or a pressure sensitive adhesive with backing plastic.

[0075] FIG. 9 depicts another implementation of reconstituted wafer 900 without gap filler according to aspects of the present disclosure. Here, the diamond dies 901 have at least one side coated with a smoothening layer 908. In some implementations the surfaces of the diamond dies on which the smoothening layer will be applied may be coated with an adhesion layer to improve the attachment of the smoothening layer to the diamond dies. The carrier may be any suitable rigid material for example in some implementations the carrier may be the logic-side wafer or the heatsink-side wafer. The carrier may be coated with an adhesive material. The adhesive material may be a UV curing adhesive, solvent curing adhesive, pressure sensitive adhesive, a thermoplastic material, or in some implementations adhesive material may correspond to a bond layer material as discussed above. The smoothening layer may then be attached to the adhesive. In implementations where the adhesive is a bond layer the smoothening layer may be permanently bonded to the carrier using the appropriate bonding method for the smoothening layer and bonding layer materials. As shown this implementation may omit the deposited gap filler material or gap filler wafer as it may provide for easier removal from the carrier and/or better suit requirements of the user.

[0076] FIG. 10 shows a reconstituted wafer heat spreader product 1000 incorporated into a Chip on Wafer on Substrate (CoWoS) system stack according to an aspect of the present disclosure. As shown in this implementation the logic-side wafer 1002 of the product is bonded to logic elements 1003 with a logic-side bond layer 1010. In some implementations, the heat spreader product 1000 may be fabricated using a diamond substrate coated with a precursor to a thermally conductive bond material where the thermally conductive bond material is compliant during bonding to a semiconductor device. The thermally conductive bond material may have thermal conductivity higher than 10 Watts per meter-kelvin) W/m-K after bonding. The bond material may contain lead, tin, indium, bismuth, zinc, gallium, or cadmium or combinations thereof. In some implementations, the bond material may be a eutectic or a transient liquid phase bond material. The precursor may contain copper, aluminum, gold, silver, nickel, silicon, germanium, lead, tin, indium, bismuth, zinc, gallium, or cadmium or combinations thereof.

[0077] The logic elements 1003 may be any circuit device that produces heat for example and without limitation, transistors, switches, resistors, inductors, lasers, diodes, capacitors, voltage regulators, integrated circuit devices, central processing units (CPUs), graphics processing units (GPUs), tensor processing units (TPUs), neural processing units (NPUs), application specific circuits (ASICs), Al chips, system on chip (SoC), field programmable gate arrays (FGPAs), photonic integrated circuits and its components (e.g. laser, detector, waveguide, modulator), silicon photonics, memory devices, such as random access memory (RAM), static RAM (SRAM), dynamic RAM (DRAM), read-only memory (ROM), volatile memory, etc. The logic side bond layer may be any material suitable to create a heat conductive interface between one or more logic elements and the logic side wafer. In some implementations the logic-side bond layer 1010 may be an adhesive or bonding material. In alternative implementations the bond layer may be omitted or may be a heat conductive material and the heat spreader product 1000 may be held in contact with the logic elements 1003 by a fastener or housing for the CoWoS system. In some implementations each entire logic element or a portion of each logic element may correspond to a hot spot in a larger integrated circuit device. Thus, the placement of the diamond dies 1001 may correspond closely with the location of these hotspots. For example, the diamond dies may be selectively placed to reduce the thermal resistance, thus limiting the temperature increase in the likely heat sensitive logic element 1003. The diamond dies may be attached to the logic-side wafer 1002 by a logic-side diamond bond layer 1010A. Similarly the diamond dies 1001 may be attached to the heatsink-side wafer 1004 by a heatsink-side diamond bond layer 1010B. Gaps between adjacent diamond dies 1001 may be fully or partially filled with gap filling material 1012.

[0078] The heat-sink side wafer 1004 and/or logic-side wafer 1002 may include one or more alignment marks 1005 or fiducials as shown. The alignment marks may be deposited onto the wafer and/or etched into the wafer to aid in the placement and alignment of the diamond dies. The fiducials or alignment marks may help in aligning the heat sink side wafer to the logic side wafer, and may help in aligning the reconstituted wafer to the IC (e.g., logic) wafer. Alignment mark size, shape, location, material etc., may differ depending upon the chosen alignment system and/or the bonding material(s) chosen. For example and without limitation, an alignment system which uses Infrared (IR) detection for alignment may be incompatible with global metal (e.g., copper) bond layers as it reflects IR radiation, yet the metal may be locally removed or patterned. Alignment marks may be placed on the diamond side of the wafers, or alignment marks may be placed on the outer surface of the reconstituted wafer. In some implementations, the logic side wafer and/or heat sink side wafer may include an alignment feature, such as a D-cut or V-notch to facilitate alignment with other wafers during subsequent processing.

[0079] Additionally, as shown the heatsink-side wafer 1004 of the product 1000 may be bonded to a heatsink 1007 with a heatsink bond layer 1014, e.g., a metallized surface suitable for a thermal interface material (TIM), silver-filled epoxy, silver sintered bond layer, or copper sintered bond layer. Examples of thermal interface materials are indium-based TIMs, solder-based TIMs, liquid metal (e.g. gallium) based TIMs, etc. The heatsink bond layer 1014 may be any material suitable to create a heat conductive interface between one or more heatsinks and the heatsink-side wafer 1004. In some implementations the heatsink bond layer may be an adhesive or bonding material. In alternative implementations the heatsink bond layer may be omitted or is a heat conductive material and the heat spreader product may be held in contact with the heatsink by a fastener or housing for the CoWoS system. The heat conductive material may be a thermal grease, thermal paste, thermal adhesive, thermal pad, carbon-based TIM (e.g. graphene or carbon nanotubes), or phase change material. The heatsink 1007 may be any material or device having sufficient size, properties and/or configuration to absorb and/or carry heat away from the CoWoS system with heat spreader product. For example and without limitation the heatsink 1007 may be, a larger heat conductive surface (e.g., a metal surface), a finned heat conductive surface (e.g., air cooling finned heat sink), heat conductive surface with heat pipes, a heat conductive surface with one side exposed to a second moving heat conductive medium (e.g., water cooling heat sink), or a heat conductive surface exposed to a heat conductive medium which changes phase (e.g., phase change cooling, and evaporative cooling). The cooling (heat sinking) may happen by air cooling, vapor chambers, heat pipes, liquid cooling, spray cooling, immersion cooling, etc.

[0080] In the implementation shown, the logic elements 1003 are part of a larger integrated circuit device. The logic elements may be communicatively coupled with an interposer 1009. The communicative coupling may be for example and without limitation, through solder connections (e.g., micro solder bumps) or conductive contact pins. The interposer may include conductive vias and lateral conductive traces to make communicative connections between different elements within the CoWoS stack. The interposer 1009 may be communicatively coupled with a package substrate 1011. The communicative coupling to the package substrate may be for example and without limitation, through solder connections (e.g., solder bumps) or conductive contact pins. The package substrate may include conductive vias and lateral conductive traces to make communicative connections between different elements connected to the package substrate within the CoWoS stack. The package substrate 1011 may be communicatively coupled with a circuit board 1013. The communicative coupling to the circuit board may be for example and without limitation, through solder connections (e.g. solder balls) or conductive contact pins. The circuit board may include conductive vias and lateral conductive traces to make communicative connections between different elements connected to the circuit board within the CoWoS stack.

[0081] It should be noted that prior to affixing the logic-side wafer 1002 to the logic elements 1003 the logic side wafer may be thinned to <100 m or <10 m. Likewise the prior to affixing the heatsink-side wafer 1004 to heatsink 1007, the heatsink-side wafer may be thinned. Similarly, the heatsink-side wafer 1004 may be thinned to <500 m, <100 m or <10 m. Generally, it may be favorable for the logic-side wafer 1002 to be thinner than heatsink-side wafer 1004 as it is closer to the heat generating elements, e.g., the logic elements 1003. It should further be understood that if the thinned wafers are extremely thin a temporary carrier may be adhered to the wafer that is first thinned to improve stability for thinning the second wafer, the temporary carrier may subsequently be removed before bonding.

[0082] Wafer thinning may be accomplished, for example and without limitation, by using one or more of the following techniques: abrasive techniques, grinding, lapping, chemical mechanical polishing (CMP), polishing (wet or dry), wet etching, dry etching, or laser ablation. The thinning process may be facilitated by, e.g., a temporary carrier with a temporary adhesive, specialized pads or tapes, or the TAIKO process. In the TAIKO process a thicker ring is left temporarily around the wafer perimeter to support the wafer. Carriers may be used with bonds that are often considered permanent, yet used as a temporary bond, and after thinning the logic side or heat sink side wafer the carrier is removed by for example and without limitation, destruction such as by grinding and polishing. Instead of temporary carriers with temporary adhesives, mobile electrostatic carriers might be used. Furthermore, buried layers may be introduced into the wafers that facilitate thinning to below 10 m, e.g. to 500 nanometers, or even to 10's nanometers. These buried layers may act as an etch stop, e.g. as used for thinning in backside power delivery processes, may facilitate laser debond, e.g. similar to EVG's IR layer release, or may facilitate film transfer similar to Soitec's SmartCut.

[0083] While the implementation depicted in FIG. 10 may represent a CoWoS system it should be understood that aspects of the present disclosure are not so limited and may be implemented in any type of integrated circuit device packaging system including but not limited to 2D, 2.1D, 2.5D, other 3D, and 3.5D packaging systems. As used herein, 2D packaging refers to a traditional method of packaging semiconductor devices where one or multiple integrated circuits (ICs) or chips are mounted side-by-side on a single (organic laminate) packaging substrate, such as a printed circuit board (PCB), without stacking them vertically. The components are arranged in a single plane, forming a two-dimensional layout. 2.5D packaging refers to a packaging technique in which multiple integrated circuit chips (sometimes called dies) are placed side-by-side on a common interposer, e.g., silicon or an organic interposer, which provides high-density interconnections between the chips. The interposer sits on a packaging substrate. 2.1D packaging refers to a packaging technique where a redistribution layer (RDL) is used instead of a silicon interposer. 3D packaging refers to a packaging technology where multiple semiconductor dies (chips) are stacked vertically on top of each other within a single package and interconnects are made vertically between stacked dies, e.g., using through-silicon vias (TSVs) therefore offering a higher packaging density than 2D, 2.1D or 2.5D packaging. 3.5D packaging refers to a packaging technique that uses a combination of vertically stacked dies and interposers.

[0084] The reconstituted wafer product may contain diamond dies with adhesion layers, diffusion barriers, smoothening layers, bonding layers, compliant layers, height-matching filler materials on the diamond dies, a wafer on the logic side, a wafer on the heat sink side, adhesion layers on one or both wafers, diffusion barriers on one or both wafers, bond layers on one or both wafers, or even smoothening layers on one or both wafers. In addition, the reconstituted wafer product may contain gap fillers between the diamond dies. Furthermore, the reconstituted wafer product may contain perimeter sealants that partially or completely seal the materials sandwiched between both wafers from the outside, so there is no exposure to these materials during the wafer processing, e.g. cleaning, thin film deposition, film densification, film surface activation, bonding, annealing, thinning, lithography and etching, bumping, and debonding temporary carriers. The sealants may be adhesives, sealants, molding compounds, polymers, thermoplastics, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, silicones, or polyimides. Similarly, spin-on glass or polymer-derived ceramics may be used, e.g. polysilazane derivatives (e.g. polyborosilazane), polysiloxane derivatives, polysilane derivatives (e.g. polycarbosilane), polysilsesquioxanes, polysilsesquiazanes, polysilylcarbodiimides, etc. The sealants may be the same materials as used for the gap fillers. The sealants may be the same bond materials as used for bonding the diamond dies, or bonding the heatsink-side wafer to the logic-side wafer, e.g., when using one or two pocketed wafers.

Bond Layers

[0085] The material of the bond layers depends partly on the bonding technique that is used and requirements of the fab that receives the reconstituted wafers. For example, some fabs prefer to avoid exposed metals, such as copper. The bond layers may be deposited on the wafers, and may be deposited on the diamond dies, e.g. on the smoothening layers.

[0086] By way of example, and not by way of limitation, Copper (Cu) may be used as a bonding layer material in TCB on one or both wafers, and as a smoothening layer on the diamond dies. Both copper and tin (Sn) may be used for transient liquid phase bonding (TLPB), e.g. tin stacked on top of copper on one or both wafers, and copper on the diamond dies. Similarly, instead of copper, either nickel, or gold, or silver may be used in this TLPB example, or instead of tin, indium (In) may be used. A solder may be used as a bonding and/or smoothening layer and/or compliant material in solder bonding on one or both wafers, either applied as a film (coating), pre-form (foil), wire, balls, or paste, e.g., SAC305, or high-temperature SnPb alloys may be used. A eutectic may be used as a bonding and/or smoothening layer and/or compliant material in eutectic bonding on one or both wafers, either applied as a film (coating), pre-form (foil), wire, balls, or paste, e.g., AuSi, AuGe, AuSn, or CuSn. Other compositions of interest may be Zn, ZnSn (e.g., eutectic), ZnAl (e.g., eutectic), aluminum-silicon eutectic (e.g., 88.3Al/11.7Si by wt.-%) at bond temperatures of roughly 575 Celsius, or e.g., the aluminum-germanium eutectic (e.g., 55Ge/45Al by wt.-%) at bond temperatures of roughly 425 Celsius, or e.g., the zinc-aluminum eutectic (e.g., 95Zn/5Al by wt.-%) at bond temperatures of roughly 385 Celsius. A brazing material may be used as a bonding and/or smoothening layer and/or compliant material in brazing bonding on one or both wafers, either applied as a film (coating), pre-form (foil), wire, balls, or paste, e.g., AuTi, AlSi, or AlZn alloys may be used. A sinter paste may be used as a bonding and/or smoothening layer and/or compliant material in sinter bonding on one or both wafers, dispensed or printed as a paste, e.g., silver paste or copper paste. A metal foil, e.g., copper or aluminum, optionally softened by annealing prior to or during bonding, may be used as a bonding and/or smoothening layer and/or compliant material during bonding (e.g., TCB) with one or both wafers, and one or both wafers optionally metallized, and the diamond dies optionally metallized, with the metallization outer surface e.g., copper, gold, silver, titanium, nickel, or chromium. Similarly, for solder bonding, eutectic bonding, compliant layer bonding, or brazing bonding, the surfaces of one or both wafers, and the diamond dies may be metallized with the outer surface copper, gold, silver, titanium, nickel, or chromium. A reactive multi-layer foil or film, e.g., repeating alternating layers of aluminum and nickel, may be used as a bonding and/or smoothening layer and/or compliant material during bonding (e.g. TCB) with one or both wafers, and one or both wafers optionally metallized, and the diamond dies optionally metallized, with the metallization outer surface e.g., copper, gold, silver, titanium, nickel, or chromium. These reactive multilayer foils or films may be initiated by a heat pulse, laser pulse, electric spark, or other means, and this initiation may result in a self-sustaining exothermic reaction raising the local temperature to aid bonding, and may produce intermetallic compounds. Other multi-layer materials may be aluminum with titanium, or titanium with amorphous silicon. Silicon may be used as a bonding layer material and/or smoothening material in SAB or ADB. Dielectrics may be used as bonding layer and/or smoothening layer materials in PAB or fusion bonding. Metals, e.g., metal foils (e.g., aluminum, zinc, solder, eutectic), may be heated to the melting point to aid bonding, or may be heated to soften without melting to aid in bonding. Adhesive bonding may be used. Adhesives may be, without limitation, silver-filled epoxies, curable thermal interface materials, e.g., based on carbon nanotubes, or graphene.

[0087] Bonding diamond dies, e.g., rough SCD, to wafers, e.g. single crystal silicon wafers, may be performed by surface melting the silicon wafer while pressing the diamond dies into the soft (e.g., liquid) silicon surface. The silicon wafer surface may be heated through the silicon wafer by adding an absorbing layer onto the silicon surface, e.g., a doped silicon surface. The silicon wafer surface may be heated through the diamond, e.g., with visible lasers that are transmitted through the diamonds, yet get absorbed by (undoped) silicon. The silicon surface may be heated with a laser, by rapid thermal processing (RTP), e-beam heating, inductive heating, Flash Lamp Annealing (FLA), PulseForge, etc. The laser may be a kW IR laser (e.g. CO.sub.2), or a kW visible laser (e.g. green or blue), or a kW UV laser (e.g. excimer). By way of example, and not by way of limitation, rough SCD dies may be bonded to the logic side wafer by silicon surface melting, and subsequently the heat sink side wafer may be attached to the diamond dies via a thick copper foil between the dies and the heat sink side wafer.

[0088] High intensity lasers may be used to illuminate-through the diamondthe interface between the diamond and silicon to heat, melt, and cause joining. Kilowatt and multi-kilowatt lasers may be used to illuminate and heat very large areas. A highly polished diamond may not be required as the high thermal conductivity of diamond may ensure that the interface temperature is kept uniform. Ideal wavelengths for heating silicon may be shorter than 1.1 micrometer, and ideally much shorter, e.g. 550 nm to 350 nm, where there are a range of fiber and fiber delivered lasers available that can deliver large, square or rectangular, spots (e.g., from Nuburu, Laserline, or Trumpf). According to the graph shown in FIG. 11, the absorption depth for these shorter wavelength lasers may be on the order of 100 nm compared to many microns near 1000 nm, ensuring that the interaction volume of the laser, silicon/diamond interface may be kept highly localized and efficient.

[0089] In an alternative method of bonding diamond to silicon wafers according to aspects of the present disclosure, a nickel metal interface may be used. A layer of nickel may be deposited between the diamond and silicon, and then the assembly may be annealed, creating two hetero-interfaces: one where nickel may form a NiC bond with the diamond, and another where it may form a NiSi bond with the silicon. The goal of this method may be promoting interdiffusion at both interfaces, resulting in a robust and durable bond. This implementation may involve depositing a controlled thickness of nickel onto either the diamond or silicon wafer, followed by the placement of the opposing material. Alternatively, the nickel may be partially or completely provided as a foil. The assembly may then be subjected to an annealing process at temperatures between 750 Celsius and 1200 Celsius. During annealing, the nickel may facilitate the formation of a strong chemical bond with both the diamond and the silicon. The interdiffusion between the NiC and NiSi interfaces may enhance the overall strength and stability of the bond, making this method particularly useful for applications where a durable, high-temperature-resistant bond between diamond and silicon may be required. Alternatively, instead of nickel, titanium, or chromium may be used. The bonding of two metal films, e.g. the nickel film on the diamond, and the nickel film on the silicon, may be accomplished by appropriate pretreatments (e.g. to remove oxide), and thermocompression bonding. In one embodiment, the nickel is deposited on both surfaces, followed by a high temperature anneal, followed by a surface treatment, followed by thermocompression bonding. In another implementation, after film deposition and surface treatment, the pair is bonded at high temperature.

[0090] The thermal conductivity of copper (foil) and its alloys may range from 80 W/m-K to 400 W/m-K (e.g., pure copper) depending on the alloy composition, and microstructure, the latter impacted by manufacturing method, and additional processing. Annealing copper (foil) may improve thermal conductivity and soften the foil for temperatures of e.g., 300 Celsius up to its melting point. Copper may be deposited as a thin film, e.g., by electroplating, electroless plating, e-beam deposition, or sputtering with a thermal conductivity close to the copper bulk thermal conductivity (400 W/m-K). Additionally, copper may be introduced as a thin foil with a thermal conductivity in the range of 80 W/m-K to 400 W/m-K. Furthermore, copper may be introduced as a paste followed by sintering with a thermal conductivity after sintering as high as 300 W/m-K. Additionally, the crystal orientation of the copper may be controlled to aid in bonding, e.g., nanotwinned (111) copper.

[0091] The thermal conductivity of aluminum (foil) and its alloys may range from 80 W/m-K to 237 W/m-K (e.g. pure aluminum) depending on the alloy composition, and microstructure, the latter impacted by manufacturing method, and additional processing. Annealing aluminum (foil) may improve thermal conductivity and soften the foil for temperatures of e.g. 300 Celsius up to its melting point. Aluminum may be deposited as a thin film, e.g., by e-beam deposition or sputtering, with a thermal conductivity close to the aluminum bulk thermal conductivity (237 W/m-K). Additionally, aluminum may be introduced as a thin foil with a thermal conductivity in the range of 80 W/m-K to 237 W/m-K.

[0092] The thermal conductivity of silicon may range from 1 W/m-K to 140 W/m-K. Amorphous silicon films may have thermal conductivities of 1 W/m-K, whereas polycrystalline silicon (films) may have thermal conductivities around 50 W/m-K, and single crystal silicon as high as 140 W/m-K, albeit heavily dependent on doping, and crystal defect concentration. Silicon may be introduced as an amorphous film, polycrystalline film, single crystal wafer, polycrystalline wafer, or as a powder. Silicon introduced as a powder may be used as gap-filler, or may be used between one or both wafers and the diamond dies. Silicon powder may be sintered or fused together by a heat source, e.g. by laser annealing.

[0093] Materials like titanium and chromium may be deposited by any suitable deposition method for example and without limitation physical vapor deposition such as sputtering. Materials like nickel, copper, tin, zinc, gold, and silver may be deposited as a film by physical vapor deposition or plating, e.g. electroplating or electroless plating. Diffusion barrier layers like TiN or TaN may be deposited by physical vapor deposition, e.g. sputtering. Indium may be deposited by vapor deposition or plating.

[0094] The placement and bonding of diamond dies to form the reconstituted wafer product may be performed by sequential dies to wafer (SD2 W) bonding, or collective dies to wafer bonding (CD2 W). The bonding of the second wafer, e.g., heatsink-side wafer, may be a separate bonding step after the SD2 W or CD2 W bonding. Alternatively, the diamond dies may be placed onto the first wafer, and the second wafer is placed onto the diamond dies, and the whole stack may be bonded by temperature and/or force in one step.

[0095] ADB and SAB are generally performed between ultrasmooth layers, e.g., silicon with a roughness (Sa) of less than 0.5 nanometers. A silicon smoothening layer may be deposited or otherwise formed on the surfaces of the diamond dies and, in some implementations, the gap filler prior to bonding. The silicon smoothening layer may be formed by thin film deposition followed by smoothening, e.g., CMP. The silicon smoothening layer may be amorphous, nanocrystalline, microcrystalline, or polycrystalline. Deposition of the silicon layer may be by any known method for example and without limitation, Physical Vapor Deposition (PVD) or chemical vapor deposition (CVD). In the SAB process the respective bonding surfaces are cleaned of contaminants, e.g., organics, metals, and particles, prior to entering the ultra-high-vacuum environment. The bonding surfaces are treated with beams of atoms or ions in an ultra-high-vacuum (UHV) environment to remove remaining contaminants (e.g., organics, metals, and oxides) and create reactive dangling bonds and typically amorphize a few nanometers of each bonding surface (e.g., 1-5 nm). Typically, Argon atoms or ions are used. Amorphizing the bonding surfaces avoids potential issues with lattice mismatch. The treated surfaces are then subject to bonding pressure (force) under UHV. The UHV environment allows for a few minutes to bring surfaces into contact and form strong (e.g. covalent) bonds. The bonding may be done at relatively low temperature, e.g., in the range of room temperature (about 25 C.). The resulting bonds are free of a significant thickness of intermediate material. As a result of the amorphization, there may be an interface region of amorphous material between the bulk crystalline silicon wafer and the silicon smoothening layer with an interface between the two amorphous materials. In some implementations SAB may be used to bond a polished diamond die to one or more of the silicon wafers without a smoothening layer and/or bond layer. SAB may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies, e.g. smoothened diamond dies with silicon smoothening layers. The silicon may be deposited by CVD, and smoothened by CMP. Optionally, there may be a laser annealing step between CVD silicon deposition and CMP to increase the crystallinity and thermal conductivity of the thin silicon film.

[0096] In ADB, the bonding surfaces are cleaned and UHV thin films (e.g., 1-5 nm) of metal (e.g., Ti) or semiconductor (e.g., Si or AlN) or oxide are formed on the bonding surfaces e.g., by sputtering of atoms, ions, neutral species, or clustered species. The thin films may be amorphous or crystalline films. Because the films are freshly created in UHV they bond together very effectively by bringing the surfaces into contact with each other and subjecting them to little or no pressure (force) and minimal/no heating. The resulting structure has at least two interfaces, one between the wafer and an interfacial bonding layer and another between the interfacial bonding layer and the smoothening layer. ADB equipment is commercially available, e.g., from Canon Anelva Corporation of Kanagawa, Japan. ADB may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies, e.g. smoothened diamond dies with silicon smoothening layers. The silicon may be deposited by CVD, and smoothened by CMP. Optionally, there may be a laser annealing step between CVD silicon deposition and CMP to increase the crystallinity and thermal conductivity of the thin silicon film. The thin films used for bonding may be titanium, silicon or an oxide.

[0097] Plasma-assisted bonding (PAB) of silicon substrates is commonly used in CMOS foundries for advanced packaging, e.g. hybrid bonding, with process temperatures from 150 C. to 400 C. PAB bonding is very mature for wafer-to-wafer bonding. Furthermore, PAB may not require ultra-high vacuum. These are all benefits of PAB. However, the PAB bond relies on dielectric films (e.g. SiO.sub.2 or SiCN) with a very low thermal conductivity (1 W/m-K) resulting in a relatively high thermal barrier resistance despite the relatively low film thickness of 100's nanometers. Thus, there may be a need to reduce the thermal resistance for PAB by further thinning the bond layers and/or increasing the thermal conductivity of these bond layers. Furthermore, PAB has strict roughness requirements (e.g. Sa<0.5 nm). PAB may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies, e.g. smoothened diamond dies with silicon or dielectric smoothening layers. The thin films used for bonding may be silicon oxide, silicon nitride, silicon carbon-nitride, or similar dielectrics. The smoothening and bonding films may be deposited by CVD, and smoothened by CMP.

[0098] Thermo-compression bonding (TCB) historically is mainly used for vertical interconnects and perimeter sealing (e.g., MEMS) with silicon at temperatures of 300 C. to 500 C. and requires significant force (e.g., 10's MPa). Typical bond line thickness for TCB is in the micrometer range (e.g. 1-10 micrometers). TCB's roughness requirements are less strict (e.g. Sa<3 nm). Process temperature and force in TCB may be reduced by improved smoothness, flatness, and cleanliness of the metal surfaces. Improved smoothness, flatness, and cleanliness may also allow for thinner films. Furthermore, coefficient-of-thermal expansion (CTE) matching of the diamond and wafers may allow a further thickness reduction of the metal films. As such, the similar CTE for silicon and diamond may be very beneficial for a further (bond) film thickness reduction when silicon wafers are used to build the reconstituted wafer product. Common materials used for metal bonding are gold and copper. Process temperature and force reduction may allow for fragile stacks (e.g., avoiding device, lateral or vertical interconnect damage), compatibility with temporary adhesives, alignment accuracy improvement, reduced warpage, reduced thermal stress, etc. TCB is a form of metal bonding that involves solids only. TCB may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies, e.g., smoothened diamond dies with copper smoothening layers. Copper may be deposited by plating onto e.g. titanium and/or nickel deposited by PVD onto the diamond dies, and the copper may be smoothened by CMP. The bond layer on the wafers may be copper with an adhesion layer (e.g., titanium), and a diffusion barrier layer (e.g., titanium nitride, nickel, etc.) between the silicon wafer and the copper. A copper foil in a range of 50 micrometers to 750 micrometers may be sandwiched between the diamond dies and the heat sink side wafer. Alternatively, a foil of aluminum may be sandwiched between the diamond dies and the heat sink side wafer. The aluminum foil may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper. Instead of a metal foil, dies or wafers of silicon carbide may be used. The silicon carbide may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper. Instead of copper for smoothening and bonding, aluminum films may be used.

[0099] In some implementations the smoothing layer may be omitted by using solders and/or eutectics with process (liquification) temperatures above 300 C. Metal bonding that involves a liquid includes solder bonding, eutectic bonding, and transient liquid phase bonding (TLPB). These liquid-based forms of metal bonding have the added benefit of further lowering temperature (e.g., 180 C. to 300 C.) and force requirements (e.g., <1 MPa), and reduced roughness requirements (e.g. Sa<100 nm). In addition, organic or polymer bonding involves deposition of a precursor, molecule, monomer, oligomer, or polymer on one or two surfaces followed by bonding. This implementation may require only metallization of the wafer (e.g., Ti/Ni) and diamond die (e.g., Ti), with no smoothening layers. Deposition may be performed by dispensing, pre-forms, or printing. Example materials for this process may be for example and without limitation lead-containing eutectics, solders, and/or brazing materials of the PbAg, PbSnAg, PbInAg, Zn, ZnSn, and ZnAl family. Some non-limiting examples include Pb90Sn5Ag5, Pb95.5Sn2Ag2.5, Pb90In5Ag5, Pb95Ag5. Other examples of TLPB bonding materials include tin or indium containing materials for example, without limitation, CuSn, NiSn, AuSn, AgSn, AgIn, and AuIn. TLPB may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies. Copper may be deposited by plating onto e.g., titanium and/or nickel deposited by PVD onto the diamond dies, and subsequently tin may be plated over the copper. The bond layer on the wafers may be copper with an adhesion layer (e.g., titanium), and a diffusion barrier layer (e.g., titanium nitride, nickel, etc.) between the silicon wafer and the copper. Optionally, tin may be plated over the copper on the silicon wafer. A copper foil in a range of 50 micrometers to 750 micrometers may be sandwiched between the diamond dies and the heat sink side wafer. Alternatively, a foil of aluminum may be sandwiched between the diamond dies and the heat sink side wafer. The aluminum foil may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper. Instead of a metal foil, dies or wafers of silicon carbide may be used. The silicon carbide may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper.

[0100] Sintering may be also used to bond the surfaces. A silver sintering paste, gold sintering paste or copper sintering paste may be applied as the bond layer. Sufficient heat and pressure may be applied at the bonding surface to cause the sintering paste to form a bond with the sintering paste. For example and without limitation, sintering with copper paste may be used. Sintering may be done at temperatures below 250 C., either with minimal force (e.g., <1 MPa), or high force (e.g., >10 MPa). The final bond line thickness may be 50 microns, or 10 microns. The sintered layer may be porous or dense. The sintered layer may have a thermal conductivity over 100 W/m-K, even over 150 W/m-K. Sintering may be used to form a reconstituted wafer product based on one or two silicon wafers bonded to diamond dies. Copper, or silver, or gold may be deposited by plating onto, e.g., titanium and/or nickel deposited by PVD onto the diamond dies. Copper, or silver, or gold may be deposited with an adhesion layer (e.g., titanium), and a diffusion barrier layer (e.g., titanium nitride, nickel, etc.) between the silicon wafer and the copper, or silver, or gold. A sintering paste, e.g., silver paste, may be placed between the silicon wafer and the diamond dies. A copper foil in a range of 50 micrometers to 750 micrometers may be sandwiched between the diamond dies and the heat sink side wafer. Alternatively, a foil of aluminum may be sandwiched between the diamond dies and the heatsink-side wafer. The aluminum foil may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper, silver, or gold. Instead of a metal foil, dies or wafers of silicon carbide may be used. The silicon carbide may be coated, e.g., with an adhesion layer, diffusion barrier layer, and copper, silver, or gold.

[0101] In implementations using adhesives the adhesive material may be any material suitable for adhering the two surfaces together. Some examples include without limitation, pressure sensitive adhesives, UV curing adhesives, thermoplastics, solvent curing adhesives, carbon-nanotube filled adhesives, graphene filled adhesive, brewerBOND material, waferBOND material, etc. These adhesives may be permanent (permanent bonding) or removed (temporary bonding) during manufacturing using the appropriate removal technique for the type of temporary adhesive. Curing of the adhesives (e.g. cross linking) may be based on heat, irradiation (e.g., UV), or water for adhesives, or based on cooldown for thermoplastic materials. The thickness of the organic bond line may be 100 nanometers, or as thin as 5 nanometers. Deposition may be performed by spin coating, spraying, dipping, or jetting. Materials may be polymers, epoxies, photoresists, benzocyclobutene (BCB) derivatives, spin-on photo-dielectrics, silicones, or polyimides. Similarly, spin-on glass or polymer-derived ceramics may be used, e.g., polysilazane derivatives (e.g., polyborosilazane), polysiloxane derivatives, polysilane derivatives (e.g., polycarbosilane), polysilsesquioxanes, polysilsesquiazanes, polysilylcarbodiimides, etc. These materials may be filled with nano-sized materials with a high thermal conductivity (and lower CTE), e.g., diamond nanopowder, aluminum nitride (AlN) nanopowder, silicon nitride (SiN.sub.x) nanopowder, beryllium oxide (BeO) nanopowder, aluminum oxide (Al.sub.2O.sub.3) nanopowder, graphite, carbon nanotubes, graphene, etc. In some implementations the powder is part of a formulation that includes additives to control stability, e.g., surfactants, and application, e.g. rheology modifiers. A non-exhausting list of additive examples are binders, anti-settling agents, dispersants, curing agents, anti-foaming agents, and thinners (e.g. solvents).

[0102] Temporary bonding may be used in multiple steps during the processing. Temporary bonding may be used for thinning the wafers. Temporary bonding may be used with thinning the heatsink side wafer. The thinned logic side wafer may be placed onto the temporary carrier prior to thinning the heatsink side wafer. The temporary carrier may be made of glass, silicon, sapphire, quartz, or silicon carbide. The temporary carrier may match in CTE with the bonded wafer or dies. The temporary carrier may have through holes, e.g., to aid in chemical or solvent debonding. The temporary carrier may be optically transparent, e.g., to aid in optical debonding. The temporary carrier may support electrostatic bonding and debonding. The temporary carrier may contain a buried layer or surface layer that supports optical debonding. The temporary adhesive may be organic. The temporary adhesive may cross-link or be a thermoplastic. The temporary adhesive may contain one coating, or more than one coating. One of these coatings may absorb light, e.g., laser, UV, or pulsed light, which aids in debonding. The temporary carrier may have alignment marks. The temporary carrier may be bonded by a permanent bonding method, e.g., SAB, ADB, PAB, or TCB. The temporary bonding may be accomplished by a mobile electrostatic carrier. The final removal of the temporary carrier may be based on (visible or IR) laser debonding, UV debonding, thermal (slide) debonding, chemical debonding, (thermo-) mechanical debonding, (thermal) solvent debonding, electrostatic debonding, or abrasive and/or chemical removal of the temporary carrier.

[0103] In some implementations bonding may utilize a multi-layer thermally reactive foil that provides instantaneous or extremely rapid heating. Such a reactive multi-layer foil may be fabricated by vapor-depositing thousands of alternating nanoscale layers of Aluminum (Al) and Nickel (Ni). When activated by a small pulse of local energy from electrical, optical or thermal sources, the foil reacts exothermically to precisely deliver localized heat up to temperatures of 1500 C. in fractions (thousandths) of a second. By way of example, and not by way of limitation, an AlNi multi-layer thermally reactive foil is sold commercially under the name NanoFoil by Indium Corporation of Clinton New York. Nanofoil is a registered trademark of Thermal Conductive Bonding, Inc. of Sacramento, California. Other foil compositions may be boron-titanium, aluminum-titanium, and titanium-silicon. In addition to the energetic multi-layer material other materials may be included in the stack that specifically melt, comply with surfaces, and react with the wafers or diamond dies to be bonded.

Gap Filler

[0104] The gap filler material may be a depositable material or a through-hole gap filler wafer as discussed above. Alternatively, the gaps are filled by the walls of one or more pocketed wafers. The gap filler material preferably has a Coefficient of Thermal Expansion (CTE) matched closely with both Si and the die containing diamond and some stiffness to support ultrathin silicon between the dies containing diamond. Additionally, it is desirable that the gap filler material is a material suitable for dicing by traditional dicing means (e.g., saw, laser, or plasma dicing) and when fully filling the gaps easily planarized. Some implementations may use gap fillers such as and without limitation: spin-on-glass (SOG), machined silicon through-hole wafer, low-CTE polyimide (2-3 ppm/C), borosilicate or silica glass in sol-gel form (3-5 ppm/C), or glass powder filled adhesives/polymers, polybenzimidazole (5 ppm/C). Additionally, in some implementations, the gap filler may help with avoiding edge rounding when smoothening the smoothening layer (e.g. CMP).

Smoothening Layer

[0105] It is often economically desirable to be able to use diamond dies with surfaces that are not perfectly smooth and with a relaxed thickness tolerance in a reconstituted wafer product. In such cases, a smoothening layer may be formed on the surface(s) of the diamond dies to accommodate for imperfections in the diamond die surface(s). The smoothening layer may deal with surface roughness, but also with dimensional (thickness) tolerances (e.g., bow, warp, flatness, total thickness variation (TTV), or target thickness). The smoothening layer allows the reconstituted wafer product to use incoming rough diamond dies with a broad range in dimensional (thickness) and roughness tolerances. After smoothening (e.g. CMP) the smoothening layer, the surfaces are smooth, and the dimensional (thickness) tolerances are tight.

[0106] Smoothening layers (either of microns thickness with high thermal conductivity, or 10's to 100's nanometers when low thermal conductivity) may include but are not limited to: Copper (plated, e.g. 15 micrometer with thermal conductivity close to 400 W/m-K), silicon (polycrystalline/microcrystalline by hot CVD of microns thickness and thermal conductivity 50 W/m-K, or amorphous silicon by colder CVD when 10's to 100's nanometers and thermal conductivity 1 W/m-K). Note here that smoothening layers may be applied to the bonding surfaces of the diamond dies and may be excluded from the gaps in between the diamond dies. The bonding surfaces of the diamond dies may be lapped and, in some implementations, polished appropriately for the chosen bonding method. For example and without limitation, application of an amorphous or nanocrystalline silicon smoothening layer may be suitable to smoothen a lapped diamond die surface whereas application of a polycrystalline silicon smoothening layer may be more suitable for a diamond die with a rougher surface and more relaxed thickness tolerances.

[0107] The thickness of the smoothening layer(s) depends on the roughness and thickness variation of the diamond die. The higher the thickness variation of incoming diamond die, the thicker the smoothening layer needs to be and the higher the thermal conductivity of the smoothening layer needs to be. The surface roughness and thickness variation of the diamond die depends on where in the diamond die fabrication process the diamond die is picked. In general terms, the further upstream one picks the diamond die from the wafering line, the rougher and larger the thickness variation and generally, the lower the cost of producing the diamond die. By way of example, and not by way of limitation, at certain early stages of diamond die fabrication, e.g., before lapping has been started or is complete, the diamond die surface may be rough, e.g., 100 nm to 300 nm mean surface roughness with high thickness variation t, e.g., 5 m<t<30 m. At an intermediate stage, e.g., after lapping is complete, the diamond die surface may be rough, e.g., less than 100 nm mean surface roughness with a tight thickness variation t, e.g., t<5 m. At a later stage, the diamond die surface may be smooth, e.g., <5 nm roughness with a tight thickness variation t, e.g., t<5 m.

[0108] The previous descriptions provide a non-limiting list of multiple permutations of smoothening layers, bond layers, diamond die surface finish, gap filler type, bond methods, and wafers for the reconstituted wafer heat spreader product and their suitability for bonding to integrated circuit device package types. The overall thickness of the reconstituted wafer product may vary. As a non-limiting example, the thickness of the reconstituted wafer product may be roughly 2,325 micrometers prior to thinning the logic side and heat sink side wafers and may be roughly 800 micrometers after thinning the logic side and heat sink side wafers. The final thickness may be the result of 300 micrometers thick diamond die, e.g. SCD, and 450 micrometers copper foil, in addition to 10 to 30 micrometers silicon on the logic side and heat sink side. The manufacturing of the reconstituted wafer product may start with full thickness wafers, e.g. 775 micrometers thick, 300 millimeters diameter silicon wafers, or may start with partially thinned wafers that are easily handled, e.g. 350 micrometers thick. Alternatively, the incoming wafers may be thicker than the standard 775 micrometers when pocketed wafers may be used for the reconstituted wafers. Thus, aspects of the present disclosure represent a heat spreader product which may include one or more reconstituted wafers. The reconstituted wafer may provide structural stability to the product allowing for easier integration.

[0109] While the above is a complete description of the preferred embodiment of the present invention, it is possible to use various alternatives, modifications and equivalents. Therefore, the scope of the present invention should be determined not with reference to the above description but should, instead, be determined with reference to the appended claims, along with their full scope of equivalents. Any feature described herein, whether preferred or not, may be combined with any other feature described herein, whether preferred or not. In the claims that follow, the indefinite article A, or An refers to a quantity of one or more of the items following the article, except where expressly stated otherwise. The appended claims are not to be interpreted as including means-plus-function limitations, unless such a limitation is explicitly recited in a given claim using the phrase means for.