Direct gang bonding methods including directly bonding first element to second element to form bonded structure without adhesive

Information

  • Patent Grant
  • 12080672
  • Patent Number
    12,080,672
  • Date Filed
    Thursday, May 14, 2020
    4 years ago
  • Date Issued
    Tuesday, September 3, 2024
    2 months ago
Abstract
A bonded structure can comprise a first element and a second element. The first element has a first dielectric layer including a first bonding surface and at least one first side surface of the first element. The second element has a second dielectric layer including a second bonding surface and at least one second side surface of the second element. The second bonding surface of the second element is directly bonded to the first bonding surface of the first element without an adhesive.
Description
BACKGROUND
Field of the Invention

The field relates to direct gang bonding methods and structures.


Description of the Related Art

In various packaging arrangements, it can be advantageous to enable the use of multiple integrated device dies within a low-profile package. For example, three-dimensional (3D) integration techniques often utilize packages in which two or more integrated device dies are stacked on top of and electrically connected to one another. Conventional methods for die thinning and/or 3D integration may have limited product yield because stresses imparted to the dies during assembly may damage dies in the stack. Moreover, it can be challenging to stack dies which have different thicknesses and which have high pin counts and which may originate from different types of substrates and/or wafers. Accordingly, there remains a continuing need for improved systems and methods for stacking integrated device dies.





BRIEF DESCRIPTION OF THE DRAWINGS

These aspects and others will be apparent from the following description of preferred embodiments and the accompanying drawing, which is meant to illustrate and not to limit the invention, wherein:



FIGS. 1A-1G are schematic side cross-sectional views of various stages of a direct bonding process, according to one embodiment.



FIG. 1E′ is another example of FIG. 1E according to one embodiment.



FIG. 1F′ is another example of FIG. 1F according to one embodiment.



FIGS. 2A-2E are schematic side cross-sectional views of various stages of a direct bonding process, according to another embodiment.



FIGS. 3A-3C illustrate various stages of a direct gang bonding process in which elements are directly bonded to one another without intervening adhesives.



FIGS. 4A-4D illustrate examples of bonded structures according to various embodiments.



FIG. 5A illustrates schematic side cross-sectional views of a bonded structure according to various embodiments.



FIGS. 5B-5D illustrate enlarged views of a portion of the bonded structure of FIG. 5A.



FIG. 6 is a schematic diagram of a system incorporating one or more bonded structures according to various embodiments.





DETAILED DESCRIPTION

Some methods of stacking integrated device dies can mount multiple first dies to a tape structure and stack second dies onto the first dies that are disposed on the tape structure. However, the use of a tape structure to support the first dies may inadequately secure the first dies to the tape structure. Moreover, in some methods, the stacked dies can be overmolded or otherwise processed into a reconstituted wafer for subsequent processing. Overmolding or other steps in the reconstitution process may induce stresses on the integrated device dies, may be costly, and/or may utilize a thick layer of low coefficient of thermal expansion (CTE) material which may be difficult to manufacture. Accordingly, there remains a continuing need for improved stacking of elements such as integrated device dies.


Various embodiments disclosed herein relate to direct gang bonding methods and structures. For example, in various embodiments, a first plurality of elements can be simultaneously directly bonded to a second plurality of elements without intervening adhesives. Prior to and during direct bonding, adjacent elements on a carrier may be spaced apart by a gap that is not filled with a filling material. The lack of a filling material during direct bonding can reduce thermal stresses that may occur if a filling material were used between adjacent elements and can also simplify the deposition process. In various embodiments, a dielectric layer can be conformally deposited over upper and side surfaces of the elements. After bonding, outer side surfaces of the dielectric layers of two bonded elements may be laterally offset relative to one another.



FIGS. 1A-1G are schematic side cross-sectional views of various stages of a method for preparing elements 3a, 3b for forming a bonded structure 1, according to one embodiment. In FIG. 1A, a first plurality of elements 3a, 3b can be mounted to an upper surface 8 of a carrier 2. In the illustrated embodiment, the elements 3a, 3b can be directly bonded to the upper surface 8 of the carrier 2 without an intervening adhesive. The carrier 2 can comprise for example, a substrate (e.g., a semiconductor substrate), an interposer, a wafer, a reconstituted wafer, or any other suitable type of carrier. In some embodiments, the carrier 2 can comprise a silicon substrate (e.g., part or all of a wafer), a glass substrate, or silicon on insulator (SOI) substrate or planar dielectric surface 8. The use of silicon, glass, or other semiconductor material for the carrier 2 can advantageously enable the upper surface 8 of the carrier 2 to be polished to a very low surface roughness so that the first elements 3a, 3b can be directly bonded to the carrier 2. In the illustrated embodiment, for example, the carrier 2 can comprise a silicon carrier with a dielectric surface, for example, an oxide layer formed on the upper surface 8. The dielectric surface or the oxide layer can be formed in any suitable manner, for example, by thermal oxidation, Plasma Enhanced Chemical Vapor Deposition (PECVD), chemical oxidation, sputtering, evaporation, atomic layer deposition (ALD), etc.


The elements 3a, 3b can comprise any suitable type of element, such as a semiconductor element. In various embodiments, the elements 3a, 3b can comprise integrated device dies (e.g., integrated circuit, dies, memory dies, microelectromechanical systems dies, sensor dies, etc.). As shown the elements 3a, 3b can include an active surface or region 6 that is patterned with active devices, such as electronic devices like transistors. One or a plurality of interconnects or vias 10 can extend through a portion of the elements 3a, 3b shown in FIG. 1A. In the step of FIG. 1A, the vias 10 can extend from a bottom surface 5 of the active region 6 into a bulk portion 4 (e.g., bulk silicon portion) of the elements 3a, 3b. The vias 10 can be connected to contact pads on the bottom surface 5 of the elements 3a, 3b that are directly bonded to corresponding contact or bond pads on the upper surface 8 of the carrier 2. The elements 3a, 3b may comprise the same type of element or different types of elements in various embodiments.


To accomplish the direct bonding, in some embodiments, the bonding surfaces of the elements 3a, 3b and the carrier 2 can be prepared for bonding. The elements 3a, 3b can be polished to a very high degree of smoothness (e.g., less than 20 nm surface roughness, less than 1 nm surface roughness, or more particularly, less than 0.5 nm roughness). In some embodiments, a bonding layer (not shown) (e.g., a dielectric such as silicon oxide) may be deposited on the active surfaces 6 of the elements 3a, 3b and polished to a very high degree of smoothness. Similarly, the bonding surface of the carrier 2 (e.g., the upper surface 8 of the carrier 2) may be polished to a very high degree of smoothness (e.g., less than 20 nm surface roughness, less than 1 nm surface roughness, or more particularly, less than 0.5 nm roughness). In some embodiments, the bonding surfaces may be fluorinated to improve bonding energy or strength between the bonding surface of the carrier 2 and the mating or bonding surfaces of elements 3a and 3b. The bonding surfaces may also include conductive features, such as conductive bond or contact pads, conductive traces or conductive dummy features. In some embodiments, the surfaces to be bonded may be terminated with a suitable species and activated prior to bonding. For example, in some embodiments, the surfaces to be bonded may be very lightly etched for activation and exposed to a nitrogen-containing solution and terminated with a nitrogen-containing species. As one example, the surfaces to be bonded may be exposed to an ammonia dip after a very slight etch, and/or a nitrogen-containing plasma (with or without a separate etch).


Once the surfaces are prepared, nonconductive field regions of the elements 3a, 3b can be brought into contact with corresponding nonconductive field regions of the carrier 2. The interaction of the activated surfaces can cause the nonconductive regions of the elements 3a, 3b to directly bond with the corresponding nonconductive regions of the carrier 2 without an intervening adhesive, without application of external pressure, without application of voltage, and about room temperature. In various embodiments, the bonding strength of the nonconductive regions can be covalent bonds that are greater than Van der Waals bonds. In various embodiments, the nonconductive regions are initially bonded at about room temperature. In some embodiments, covalent bonding can occur during a natural anneal at about room temperature or during a heated anneal. In some embodiments, the interconnects or vias 10 and/or the contact pads are flush or slightly recessed relative to the exterior surfaces of the elements 3a, 3b and the carrier 2. In other embodiments, one of the interconnects 10 and/or the contact pads may extend above the exterior surfaces of the elements 3a, 3b and the carrier 2. In still other embodiments, the interconnects 10 and/or the contact pads are recessed relative to the exterior surfaces (e.g., oxide field regions) of the elements 3a, 3b and the carrier 2. Depending on the depth and width of the conductive features 10, the recess may range between 1 to 40 nm. The bonded structure 1 can be annealed after the nonconductive regions are bonded to create contact and a direct bond between opposing conductive regions (e.g., between opposing contact pads) without an intervening adhesive. The bonded structure 1 can be annealed after the nonconductive regions are bonded to create contact and a direct bond between opposing conductive regions (e.g., between opposing contact pads) without an intervening adhesive. In various embodiments, the carrier 2 and elements 3a, 3b may be heated after bonding to strengthen the bonds between the nonconductive regions, between the conductive regions, and/or between opposing conductive and non-conductive regions, to cause the elements 3a, 3b to bond with the carrier 2. Additional details of the direct bonding processes may be found throughout U.S. Pat. Nos. 7,126,212; 8,153,505; 7,622,324; 7,602,070; 8,163,373; 8,389,378; 8,735,219; 9,953,941; and 10,204,893, and throughout U.S. Patent Publication No. US 2017/0200711, the contents of each of which are hereby incorporated by reference herein in their entirety and for all purposes.


Turning to FIG. 1B, a sacrificial filler material 9 can be provided over the elements 3a, 3b and the upper surface 8 of the carrier 2, and filling the space between the elements 3a, 3b. The sacrificial filler material 9 can comprise any suitable type of temporary or sacrificial material that can be removed by way of subsequent processing. For example, in various embodiments, the sacrificial material 9 can comprise a photoresist material, such as a hard baked photoresist, a spin on polymer coating, an adhesive film, polyimide, etc. In FIG. 1C, the partially-formed structure 1 can be thinned. For example, a portion of the sacrificial material 9 and a portion of the elements 3a, 3b can be selectively removed to thin the structure 1. For example, an upper surface of the sacrificial material 9 can be grinded, polished, dry etched with a plasma process, or wet etched with a chemical to expose upper sides of the elements 3a, 3b. In various embodiments, grinding and chemical mechanical polishing (CMP) can be used to remove the upper portion of the sacrificial filler material 9 and upper portions of the elements 3a, 3b. The portions of the upper sides of the elements 3a, 3b can also be removed to expose the interconnects or vias 10 at an exposed upper surface 11 of bulk portions 4 of the elements 3a, 3b. As illustrated in FIG. 1C, a portion of the interconnects 10 can protrude from a surface of the bulk portions 4. In some arrangements, the sacrificial filler material 9 may facilitate planarization of the exposed surfaces 11 of the elements 3a, 3b while reducing stresses on the corners of elements 3a, 3b.


In FIG. 1D, the sacrificial filler material 9 can be removed such that no filler material is disposed over or between the elements 3a, 3b. For example, the sacrificial filler material 9 can be removed by a wet or dry etching process, a plasma etching process, a stripping process, etc. In arrangements in which there is no sacrificial material, the upper corners or edges between the horizontal and vertical portions of element 3a and 3b may crack or chip off if gentle pressures are not utilized during the thinning and polishing of the backsides of element 3a and 3b. In FIG. 1D, the elements 3a, 3b can be separated by a gap 7. The gap 7 may not include a filling material, for example, the gap 7 may be filled with a gas (such as air) or may be under vacuum. Turning to FIG. 1E, a dielectric material comprising a dielectric layer 12 can be deposited over the elements 3a, 3b and over portions of the upper surface 8 of the carrier 2 disposed between adjacent elements 3a, 3b. In some embodiments, the dielectric layer 12 may comprise a conformal dielectric coating, as illustrated in FIG. 1E′. For example, a portion of the dielectric layer 12 above the protruded via 10 can be higher than area surrounding the portion. In some applications, the thickness of the dielectric layer 12 is smaller than the thickness of elements 3a or 3b. The dielectric layer 12 can serve as a protective material to protect the upper and side surfaces of the elements 3a, 3b. The dielectric layer 12 can also be selected to serve as a nonconductive bonding layer or region for subsequent direct bonding steps. The dielectric layer 12 can comprise any suitable type of dielectric material. For example, in various embodiments, the dielectric layer 12 can comprise silicon oxide, silicon nitride, silicon oxynitride, silicon carbide, or any other suitable dielectric. In some embodiments, the dielectric layer 12 may comprise multiple layers of different dielectric materials. At the edge of the die, the dielectric layer 12 can cover debris or cracks weakly bonded due to die singulation and which might negatively impact the bond. As shown the gap 7 can be disposed between portions of the dielectric layer 12 disposed on sidewalls of adjacent elements 3a, 3b.


A second sacrificial filler material 13 can be provided over the dielectric layer 12 including the gaps 7 in FIG. 1F. In some embodiments, the second sacrificial layer 13 may comprise a dielectric coating, as illustrated in FIG. 1F′. As with the sacrificial filler material 9, the second sacrificial filler material 13 can facilitate thinning of the partially-formed bonded structure 1. Turning to FIG. 1G, the partially-formed bonded structure 1 can be thinned. For example, an upper portion of the second sacrificial filler material 13 and upper portions of the dielectric layer 12 can be selectively removed, for example, by polishing, grinding, etc. In some embodiments, the second sacrificial material 13 can be then completely removed. As shown in FIG. 1G, only a portion of the dielectric layer 12 can be removed, so as to expose the vias 10 at an exposed upper portion 14 of the dielectric layer 12.



FIGS. 2A-2E are schematic side cross-sectional views of various stages of a method for forming a preliminary bonded structure 1, according to another embodiment. Unless otherwise noted, the components of FIGS. 2A-2E may be the same as or generally similar to like-numbered components of FIGS. 1A-1G. In FIG. 2A, a carrier 2 can be provided. As shown in FIG. 2B, as with FIG. 1A, elements 3a, 3b can be directly bonded to the carrier 2 without an intervening adhesive. Moving to FIG. 2C, the preliminary bonded structure 1 can be thinned, for example, upper surfaces of the elements 3a, 3b, for example the bulk portion 4, can be selectively removed (e.g., by grinding, polishing, dry etched with a plasma process, or wet etched with a chemical) without providing a sacrificial filler material over and between the elements 3a, 3b. Thus, in some embodiments, the elements 3a, 3b can be planarized to expose the vias 10 at exposed surface 11 without using a sacrificial filler material. As illustrated in FIG. 2C, a portion of the vias 10 can protrude from the exposed surface 11. As with FIG. 1E or 1E′, the dielectric layer 12 can be provided over the elements 3a, 3b in FIG. 2D. An upper portion of the dielectric layer 12 can be removed (for example, by polishing, grinding, etc.) to expose the vias 10 at the exposed upper portion 14 of the dielectric layer 12. As with the embodiment of FIGS. 1A-1G, once the vias 10 are exposed, a gap 7 may be provided between the elements 3a, 3b as shown in FIG. 2E.



FIGS. 3A-3C illustrate various stages of a direct gang bonding process in which a first plurality of elements 3a, 3b is direct bonded to a corresponding second plurality of elements 3a′, 3b′ without intervening adhesives. In some embodiments, the bonding process illustrated in FIGS. 3A-3C can be used for a wafer to wafer bonding process, in which each wafer includes numerous elements to be directly bonded. Unless otherwise noted, components of FIGS. 3A-3C may be the same as or generally similar to like-numbered components of FIGS. 1A-2D. For example, in FIG. 3A, the exposed upper surfaces 14, 14′ of the dielectric layers 12, 12′ of the elements 3a, 3b, 3a′, 3b′ can be prepared for direct bonding as explained above in connection with FIG. 1A. In various embodiments, the processes described in connection with FIGS. 1G and 2E may be used to at least partially prepare the surfaces of the dielectric layer 12 for bonding. Additional processing may be performed to prepare the dielectric layer 12 and the contact pads connected to the exposed portion of the vias 10 for direct bonding. For example, in some embodiments, the surfaces 14, 14′ to be bonded may be very lightly etched for activation and exposed to a nitrogen-containing solution and terminated with a nitrogen-containing species. For example, oxygen reactive ion etching plasma and nitrogen radical activation may be used. As another example, the surfaces 14, 14′ to be bonded may be exposed to an ammonia dip after a very slight etch, and/or a nitrogen-containing plasma (with or without a separate etch). Further, in some embodiments, a pre-process for direct bonding may be performed. For example, the pre-process may include a surface cleaning process such as a vacuum ultraviolet irradiation, a vacuum ultraviolet/ozone irradiation, sulfuric-peroxide mixture (SPM) cleaning process, etc.


In FIG. 3B, the elements 3a′ and 3b′ may be simultaneously brought into direct contact with the elements 3a, 3b. For example, once the surfaces 14, 14′ are prepared, nonconductive field regions of the elements 3a, 3b can be brought into contact with each other. The interaction of the activated surfaces can cause the nonconductive regions of the elements 3a, 3b to directly bond with the corresponding nonconductive regions of the elements 3a, 3b without an intervening adhesive, without application of external pressure, without application of voltage, and about room temperature. In various embodiments, the bonding strength of the nonconductive regions can be covalent bonds that are greater than Van der Waals bonds. In some embodiments, covalent bonding can occur between the surfaces 14, 14′. The bonded structure 1 can be annealed after directly bonding the surfaces 14, 14′.


In some embodiments, the structure of FIG. 3B can be annealed at elevated temperature to enhance the bond strength of the non-conductive area around via 10 and to form direct metal-to-metal bonding of the vias 10 (or contact pads connected to the vias 10). Thus, in FIG. 3B, the element 3a′ can be directly bonded to the element 3a along a bond interface 15 without an intervening adhesive. The element 3b′ can be directly bonded to the element 3b along a bond interface 15 without an intervening adhesive. In some embodiments, the same or a generally similar method of directly bonding the elements 3a, 3b and the carrier 2 can be used for bonding the elements 3a′, 3b′ and the elements 3a, 3b, respectively.


As shown, prior to and during direct bonding of the elements 3a, 3a′, 3b, 3b′, the elements 3a, 3b (and also the elements 3a′, 3b′) may occlude the gap 7 in which no filling material is disposed. Rather, as shown in FIGS. 3A-3B, the gap 7 may be filled with a gas (such as air) or under vacuum. Beneficially, the absence of filling material during bonding can reduce stresses on the elements 3a, 3b that may be introduced during heating due to different coefficients of thermal expansion (CTE) of the filling material(s) and may reduce the number of process steps, thus lowering fabrication costs.


Turning to FIG. 3C, the carrier 2′ to which the elements 3a′, 3b′ are bonded may be removed. As shown in FIG. 3C, the elements 3a, 3a′ and 3b, 3b′ may be slightly laterally offset relative to one another, due to, for example, inaccuracies in the alignment process. The carrier 2′ can be removed in any suitable manner, for example, by etching, grinding, polishing, etc. In some embodiments, the carrier 2 to which the elements 3a, 3b are bonded may also be removed. As shown in FIG. 3C, the dielectric layer 12′ on the element 3a′ can define a first outer surface 17a, and the dielectric layer 12 on the element 3b can define a second outer surface 17b. In some embodiments, the bonded structure 1 of FIG. 3C can be integrated into the larger electronic system, for example, by mounting the bonded structure 1 to a system or motherboard. In some embodiments, therefore, the first and second outer surfaces 17a, 17b can be exposed on an exterior surface of the bonded structure 1. As shown in FIG. 3C, an overhanging portion 13′ of the dielectric layer 12′ can remain after the removal of the carrier 2′, and can overhang the bonded structure. As shown in FIGS. 5B-5C, the overhanging portion of the dielectric layer 12 may break off during subsequent processing.



FIGS. 4A-4D illustrate examples of bonded structures 1 during various stages of a stacking process. Unless otherwise noted, components of FIGS. 4A-4D may be the same as or generally similar to like-numbered components of FIGS. 1A-3C. In some embodiments, the same or a generally similar method of directly bonding the elements 3a, 3b associated with FIGS. 1A-3C can be used. In FIG. 4A, for example, the gap 7 between the elements 3a, 3a′, 3b, 3b′ produced in FIG. 3C can be filled with a filling material 16, such as a molding compound. The filling material 16 can protect the elements 3a, 3a′, 3b, 3b′ during a subsequent process or during operation. The filling material 16 can be applied within the gaps disposed between adjacent stacked structures. For example, the filling material 16 can be applied in a flowable form, and can be hardened by/after curing. The filling material 16 can be applied after the elements 3a, 3a′ and the elements 3b, 3b′ are direct bonded, such that the filling material 16 can comprise a seamless filler. For example, the filling material 16 can comprise a single layer of filler. In other embodiments, however, no filling material can be applied, and the bonded structure 1 of FIG. 3C can be integrated into the larger electronic system.


As shown in FIG. 4B, the bonded structure 1 of FIG. 4A can be singulated along saw lines between the elements 3a, 3b and between the elements 3a′, 3b′ to form a singulated bonded structure 1. Thus, in the singulated bonded structure 1 of FIG. 4B, the filling material 16 can be disposed along the side surfaces of the singulated bonded structure 1. The filling material 16 can comprise markings indicative of a sawing process or other methods such as laser stealth dicing or laser ablation used during singulation. The carrier 2 may remain bonded to the elements 3a, 3b for integration into the larger electronic system or device in some embodiments. For example, the carrier 2 can be bonded (e.g., direct bonded or adhered with an adhesive such as solder) to a motherboard of the larger electronic system. In other embodiments, as shown in FIG. 4C, the carrier 2 can be removed such that the elements 3a, 3b and/or 3a′, 3b′ can be bonded to the motherboard of the larger electronic system.



FIG. 4D illustrates a bonded structure 1 in which more than two elements are bonded together to form a stacked bonded structure. For example, in FIG. 4D, element 3a″ can be directly bonded to element 3a′, and element 3a′″ can be directly bonded to element 3a″. The interconnects or vias 10 can provide vertical electrical communication among the elements 3a-3a′″. Although four elements 3a-3a′″ are shown in FIG. 4D, in other embodiments, more or fewer than four elements can be provided. In the embodiment of FIG. 4D, the outer side surfaces defined at least in part by the dielectric layers 12, 12′, 12″, 12′″ can be exposed on the exterior surface of the bonded structure 1. In other embodiments, as with FIGS. 4A-4C, a filling material can be provided between the bonded structures such that, in FIG. 4D, the filling material can be disposed alongside surfaces of the dielectric layers 12, 12′, 12″, 12′″.



FIG. 5A illustrates a bonded structure 1 prior to singulation. FIGS. 5B-5D illustrate magnified portions of the bonded structure 1 of FIG. 5A. Unless otherwise noted, components of FIGS. 5A-5D may be the same as or generally similar to like-numbered components of FIGS. 1A-4D. As explained above, in various embodiments, one or both carriers 2, 2′ can be removed from the bonded structure. For example, the carrier(s) 2 and/or 2′ can be removed by etching, grinding, polishing, or any other suitable removal method. When the carrier 2′ is separated from the dielectric layer 12′, a portion of the dielectric layer 12′ can fracture or break away from the carrier 2′. The breaking away of the carrier 2′ from the dielectric layer 12′ can form a fractured surface (or structure) 18a or 18b in the dielectric layer 12′. For example, as shown in FIG. 5B, in some cases, the fractured surface 18a can comprise a concave surface in which a portion of the dielectric material 12′ along side surfaces 20 of the element 3a′ is removed. In other cases, as shown in FIG. 5C, a fractured surface 18b can comprise a concave surface or projection that extends outwardly from the side of the bonded structure 1. As shown in FIGS. 5B and 5C, the fractured surface (or structure) 18a or 18b can be disposed at a portion of the dielectric layer 12′ at or near a surface of the element 3a′ opposite the bonding interface 15 between the elements 3a, 3a′. In some embodiments, when the carrier 2′ is separated from the dielectric layer 12′, an interface where the element 3a′ and the dielectric layer 12′ meet can fracture or break away from the carrier 2′ (not illustrated). Still in some embodiments portions dielectric layer 12′ abutting carrier 2′ may be selectively removed (not illustrated) prior to the bond of the horizontal surface of elements 3a and 3b to the respective counterparts 3a′ and 3b′. The selective removal of selected portions of dielectric layer 12′ from the surface of carrier 2′ reduces the incidence of fractures of FIGS. 5B and 5C during the removal of carrier 2′.


Turning to FIG. 5D, as explained above, the dielectric layers 12, 12′ can coat (e.g., conformally coat in some embodiments) side surfaces 20 of the elements 3a, 3a′ and the exposed upper surfaces 11, 11′ of the respective elements 3a, 3a′. For example, as shown in FIG. 5D, upper portions 12a′ of the dielectric layers 12′ can be provided over the exposed upper surfaces 11, 11′ of the respective elements 3a, 3a′. The upper portion 12a of the dielectric layer 12 on the element 3a can be directly bonded without an intervening adhesive to the corresponding upper portion 12a′ of the dielectric layer 12′ on the element 3a′. Further, as shown in FIG. 5D, the dielectric layers 12, 12′ can be rounded or curved along curved surfaces 19, 19′ that are disposed between the side surfaces 20, 20′ and the upper surfaces 11, 11′ of the elements 3a, 3a′. For example, the first dielectric layers 12, 12′ is curved along an edge or corner of the first and the second element 3a, 3a′ between the first and second bonding surfaces and the at least one first and second side surface. As explained above, the elements 3a, 3a′ may be slightly misaligned such that, after direct bonding, side surfaces 20, 20′ of the elements 3a, 3a′ and outer surfaces 17a, 17b of the dielectric layers 12, 12′ are laterally offset relative to one another by an offset distance d. The offset distance d can be less than 2 μm, less than 5 μm, or less than 10 μm, for example, in a range of 0.2 μm to 10 μm, in a range of 0.2 μm to 5 μm, in a range of 0.2 μm to 2 μm, or in a range of 0.2 μm to 1 μm. In various embodiments the offset distance d can be less than the width of the via 10 or other contact pads which are connected to one another (which as explained above can result from misalignment between the top and bottom elements or dies). In various embodiments, for example, the offset distance d can be substantially smaller than a width of the contact pads or vias 10. For example, the offset distance d can be less than 95% of the width of contact pads or vias 10, or less than 60% of the width of contact pads or vias 10. The offset distance d may be sufficiently small such that contact pads connected to the interconnects 10 maintain direct contact after bonding. In some embodiment, the offset distance d is less than 5% of the thickness of the elements 3a or 3b, for example, less than 10% of the thickness of the elements 3a, 3b.



FIG. 6 is a schematic diagram of a system 80 incorporating one or more bonded structures 1, according to various embodiments. The system 80 can comprise any suitable type of electronic device, such as a mobile electronic device (e.g., a smartphone, a tablet computing device, a laptop computer, etc.), a desktop computer, an automobile or components thereof, a stereo system, a medical device, a camera, or any other suitable type of system. In some embodiments, the electronic device can comprise a microprocessor, a graphics processor, an electronic recording device, or digital memory. The system 80 can include one or more device packages 82 which are mechanically and electrically connected to the system 80, e.g., by way of one or more motherboards. Each package 82 can comprise one or more bonded structures 1. The bonded structures 1 shown in FIG. 6 can comprise any of the bonded structures 1 shown and described above in connection with FIGS. 1A-5D. The bonded structure 1 can include one or more integrated device dies which perform various functions for the system 80.


For purposes of summarizing the disclosed embodiments and the advantages achieved over the prior art, certain objects and advantages have been described herein. Of course, it is to be understood that not necessarily all such objects or advantages may be achieved in accordance with any particular embodiment. Thus, for example, those skilled in the art will recognize that the disclosed implementations may be embodied or carried out in a manner that achieves or optimizes one advantage or group of advantages as taught or suggested herein without necessarily achieving other objects or advantages as may be taught or suggested herein.


All of these embodiments are intended to be within the scope of this disclosure. These and other embodiments will become readily apparent to those skilled in the art from the following detailed description of the embodiments having reference to the attached figures, the claims not being limited to any particular embodiment(s) disclosed. Although this certain embodiments and examples have been disclosed herein, it will be understood by those skilled in the art that the disclosed implementations extend beyond the specifically disclosed embodiments to other alternative embodiments and/or uses and obvious modifications and equivalents thereof. In addition, while several variations have been shown and described in detail, other modifications will be readily apparent to those of skill in the art based upon this disclosure. It is also contemplated that various combinations or sub-combinations of the specific features and aspects of the embodiments may be made and still fall within the scope. It should be understood that various features and aspects of the disclosed embodiments can be combined with, or substituted for, one another in order to form varying modes of the disclosed implementations. Thus, it is intended that the scope of the subject matter herein disclosed should not be limited by the particular disclosed embodiments described above, but should be determined only by a fair reading of the claims that follow.

Claims
  • 1. A method of forming a bonded structure, the method comprising: forming a first dielectric layer on a first element and on a third element, the first dielectric layer being formed on an upper surface and a side surface of each of the first and the third elements;forming a second dielectric layer on a second element and on a fourth element, the second dielectric layer being formed on an upper surface and a side surface of each of the second and fourth elements;polishing a surface of the first dielectric layer; anddirectly bonding the polished surface of a first portion of the first dielectric layer that is disposed on the first element to a first portion of the second dielectric layer that is disposed on the second element to form a first bonded structure without an adhesive, and directly bonding the polished surface of a second portion of the first dielectric layer that is disposed on the third element to a second portion of the second dielectric layer that is disposed on the fourth element to form a second bonded structure without an adhesive, wherein the first bonded structure is spaced from the second bonded structure by a gap.
  • 2. The method of claim 1, wherein before forming the first dielectric layer, directly bonding the first element and the third element to a first carrier without an intervening adhesive and directly bonding the second element and the fourth element to the second carrier without an intervening adhesive.
  • 3. The method of claim 2, further comprising, after directly bonding the polished surface of the first portion of the first dielectric layer to the first portion of the second dielectric layer and the polished surface of the second portion of the first dielectric layer to the second portion of the second dielectric layer, removing the first carrier from the first element and the third element.
  • 4. The method of claim 1, further comprising, after directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer, providing a filling material in the gap between the first and second bonded structures.
  • 5. The method of claim 1, further comprising, after directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer, singulating the bonded structure along the gap to physically separate the first and second bonded structures.
  • 6. The method of claim 1, wherein directly bonding the polished surface of the first portion of the first dielectric layer to the first portion of the second dielectric layer comprises directly hybrid bonding the polished surface of the first portion of the first dielectric layer to the first portion of the second dielectric layer, and wherein directly bonding the polished surface of the second portion of the first dielectric layer to the second portion of the second dielectric layer comprises directly hybrid bonding the polished surface of the second portion of the first dielectric layer to the second portion of the second dielectric layer.
  • 7. The method of claim 1, wherein the gap is filled with a gas or under vacuum.
  • 8. The method of claim 1, further comprising providing a filling material in the gap.
  • 9. A method of forming a bonded structure, the method comprising: forming a first dielectric layer on a first element and on a third element, a first portion of the first dielectric layer being formed on an upper surface of each of the first and third elements and a second portion of the first dielectric layer being formed on a side surface of each of the first and the third elements;forming a second dielectric layer on a second element and on a fourth element, a first portion of the second dielectric layer being formed on an upper surface of each of the second and fourth elements and a second portion of the second dielectric layer being formed on a side surface of each of the second and fourth elements;thinning the first element and the third element to expose a conductive via in the first element and the third element; andafter the thinning, directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer to form a first bonded structure, and directly bonding the second portion of the first dielectric layer to the second portion of the second dielectric layer to form a second bonded structure without an adhesive, wherein the first bonded structure is spaced from the second bonded structure by a gap.
  • 10. The method of claim 9, further comprising, before directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer, forming the first dielectric layer and the second dielectric layer as a conformal layer.
  • 11. The method of claim 10, further comprising removing a portion of the first dielectric layer to expose the conductive via through the first dielectric layer.
  • 12. The method of claim 11, further comprising: before directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer, and after the thinning, providing a sacrificial material over the first dielectric layer; andremoving the sacrificial material after the removing the portion of the first dielectric layer.
  • 13. The method of claim 9, further comprising: before directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer, and before the thinning, providing a sacrificial material over the first and third elements; andremoving the sacrificial material after the thinning.
  • 14. The method of claim 9, wherein directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer comprises directly hybrid bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer and the second portion of the first dielectric layer to the second portion of the second dielectric layer.
  • 15. The method of claim 9, wherein the gap is filled with a gas or under vacuum.
  • 16. The method of claim 9, further comprising providing a filling material in the gap.
  • 17. A method of forming a bonded structure, the method comprising: depositing a first dielectric layer over a first plurality of singulated elements mounted to a first carrier and spaced apart from one another by one or more respective first gaps, each of the first plurality of singulated elements comprises an integrated device die, the first dielectric layer being formed on an upper surface and at least a portion of a side surface of each of the first plurality of singulated elements;depositing a second dielectric layer over a second plurality of singulated elements mounted to a second carrier and spaced apart from one another by one or more respective second gaps, the second dielectric layer being formed on an upper surface and at least a portion of a side surface of each of the second plurality of singulated elements; anddirectly gang bonding the first dielectric layer without an adhesive to form a plurality of bonded structures, wherein adjacent bonded structures of the plurality of bonded structures are spaced apart by a gap.
  • 18. The method of claim 17, further comprising directly bonding the first plurality of singulated elements to the first carrier without an adhesive and directly bonding the second plurality of singulated elements to the second carrier without an adhesive.
  • 19. The method of claim 17, wherein the second plurality of singulated elements comprise integrated device dies.
  • 20. The method of claim 17, wherein directly gang bonding the first dielectric layer to the second dielectric layer without an adhesive comprises directly hybrid bonding the first dielectric layer to the second dielectric layer.
  • 21. The method of claim 17, wherein the one or more respective first gaps is filled with a gas or under vacuum and the one or more respective second gaps is filled with a gas or under vacuum.
  • 22. The method of claim 17, further comprising providing a filling material in the gap.
  • 23. A method of forming a bonded structure, the method comprising: directly bonding first and third singulated elements to a first carrier without an intervening adhesive, at least the first singulated element comprises an integrated device die, the first and third singulated elements are spaced apart by a gap;directly bonding second and fourth elements to a second carrier without an intervening adhesive;while the first singulated element is directly bonded to the first carrier and the second element is directly bonded to the second carrier, directly bonding a first portion of a first dielectric layer disposed on the first singulated element to a first portion of a second dielectric layer disposed on the second element without an intervening adhesive; andwhile the third singulated element is directly bonded to the first carrier and the fourth element is directly bonded to the second carrier, directly bonding a second portion of the first dielectric layer disposed on the third singulated element to a second portion of the second dielectric layer disposed on the fourth element without an intervening adhesive.
  • 24. The method of claim 23, further comprising removing the second carrier after directly bonding the respective first portions and the respective second portions.
  • 25. The method of claim 23, further comprising a gap between the second and fourth elements.
  • 26. The method of claim 23, wherein the second and fourth elements are singulated elements,directly bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer comprises directly hybrid bonding the first portion of the first dielectric layer to the first portion of the second dielectric layer; anddirectly bonding the second portion of the first dielectric layer to the second portion of the second dielectric layer comprises directly hybrid bonding the second portion of the first dielectric layer to the second portion of the second dielectric layer.
  • 27. The method of claim 23, wherein the gap is filled with a gas or under vacuum.
  • 28. The method of claim 23, further comprising providing a filling material in the gap.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application No. 62/906,608, filed Sep. 26, 2019, the entire contents of which are incorporated by reference in their entirety and for all purposes.

US Referenced Citations (385)
Number Name Date Kind
4998665 Hayashi Mar 1991 A
5019673 Juskey et al. May 1991 A
5087585 Hayashi Feb 1992 A
5322593 Hasegawa et al. Jun 1994 A
5753536 Sugiyama et al. May 1998 A
5771555 Eda et al. Jun 1998 A
5956605 Akram et al. Sep 1999 A
5985739 Plettner et al. Nov 1999 A
5998808 Matsushita Dec 1999 A
6008126 Leedy Dec 1999 A
6080640 Gardner et al. Jun 2000 A
6121688 Akagawa Sep 2000 A
6265775 Seyyedy Jul 2001 B1
6374770 Lee Apr 2002 B1
6423640 Lee et al. Jul 2002 B1
6465892 Suga Oct 2002 B1
6582991 Maeda et al. Jun 2003 B1
6887769 Kellar et al. May 2005 B2
6908027 Tolchinsky et al. Jun 2005 B2
7045453 Canaperi et al. May 2006 B2
7078811 Suga Jul 2006 B2
7105980 Abbott et al. Sep 2006 B2
7126212 Enquist et al. Oct 2006 B2
7193423 Dalton et al. Mar 2007 B1
7262492 Pieda et al. Aug 2007 B2
7354798 Pogge et al. Apr 2008 B2
7750488 Patti et al. Jul 2010 B2
7781309 Morita Aug 2010 B2
7790578 Furui Sep 2010 B2
7803693 Trezza Sep 2010 B2
7843052 Yoo et al. Nov 2010 B1
7932616 Meguro Apr 2011 B2
8026181 Arita et al. Sep 2011 B2
8178963 Yang May 2012 B2
8178964 Yang May 2012 B2
8183127 Patti et al. May 2012 B2
8241961 Kim et al. Aug 2012 B2
8314007 Vaufredaz Nov 2012 B2
8349635 Gan et al. Jan 2013 B1
8377798 Peng et al. Feb 2013 B2
8441131 Ryan May 2013 B2
8476146 Chen et al. Jul 2013 B2
8476165 Trickett et al. Jul 2013 B2
8482132 Yang et al. Jul 2013 B2
8501537 Sadaka et al. Aug 2013 B2
8513088 Yoshimura et al. Aug 2013 B2
8524533 Tong et al. Sep 2013 B2
8620164 Heck et al. Dec 2013 B2
8647987 Yang et al. Feb 2014 B2
8697493 Sadaka Apr 2014 B2
8716105 Sadaka et al. May 2014 B2
8802538 Liu Aug 2014 B1
8809123 Liu et al. Aug 2014 B2
8841002 Tong Sep 2014 B2
8975163 Lei et al. Mar 2015 B1
8988299 Kam et al. Mar 2015 B2
9059010 Yoshida et al. Jun 2015 B2
9076860 Lei et al. Jul 2015 B1
9076929 Katsuno et al. Jul 2015 B2
9093350 Endo et al. Jul 2015 B2
9142517 Liu et al. Sep 2015 B2
9171756 Enquist et al. Oct 2015 B2
9184125 Enquist et al. Nov 2015 B2
9224704 Landru Dec 2015 B2
9230941 Chen et al. Jan 2016 B2
9257399 Kuang et al. Feb 2016 B2
9299736 Chen et al. Mar 2016 B2
9312229 Chen et al. Apr 2016 B2
9331149 Tong et al. May 2016 B2
9337235 Chen et al. May 2016 B2
9343433 Lee et al. May 2016 B2
9355997 Katkar et al. May 2016 B2
9368866 Yu Jun 2016 B2
9385024 Tong et al. Jul 2016 B2
9394161 Cheng et al. Jul 2016 B2
9437572 Chen et al. Sep 2016 B2
9443796 Chou et al. Sep 2016 B2
9461007 Chun et al. Oct 2016 B2
9466586 Choi et al. Oct 2016 B1
9496239 Edelstein et al. Nov 2016 B1
9536848 England et al. Jan 2017 B2
9559081 Lai et al. Jan 2017 B1
9570421 Wu et al. Feb 2017 B2
9620481 Edelstein et al. Apr 2017 B2
9653433 Yu et al. May 2017 B2
9656852 Cheng et al. May 2017 B2
9673096 Hirschler et al. Jun 2017 B2
9674939 Scannell Jun 2017 B2
9722098 Chung et al. Aug 2017 B1
9723716 Meinhold Aug 2017 B2
9728521 Tsai et al. Aug 2017 B2
9741620 Uzoh et al. Aug 2017 B2
9799587 Fujii et al. Oct 2017 B2
9818729 Chiu et al. Nov 2017 B1
9852988 Enquist et al. Dec 2017 B2
9865567 Chaware et al. Jan 2018 B1
9881882 Hsu et al. Jan 2018 B2
9893004 Yazdani Feb 2018 B2
9899442 Katkar Feb 2018 B2
9929050 Lin Mar 2018 B2
9941241 Edelstein et al. Apr 2018 B2
9941243 Kim et al. Apr 2018 B2
9953941 Enquist Apr 2018 B2
9960142 Chen et al. May 2018 B2
10008844 Wang et al. Jun 2018 B2
10026605 Doub et al. Jul 2018 B2
10075657 Fahim et al. Sep 2018 B2
10204893 Uzoh et al. Feb 2019 B2
10269756 Uzoh Apr 2019 B2
10276619 Kao et al. Apr 2019 B2
10276909 Huang et al. Apr 2019 B2
10333623 Liao Jun 2019 B1
10410976 Asano et al. Sep 2019 B2
10418277 Cheng et al. Sep 2019 B2
10446456 Shen et al. Oct 2019 B2
10510629 Chen et al. Dec 2019 B2
10707087 Uzoh et al. Jul 2020 B2
10707145 Bultitude et al. Jul 2020 B2
10727204 Agarwal et al. Jul 2020 B2
10727219 Uzoh et al. Jul 2020 B2
10770430 Kim et al. Sep 2020 B1
10790262 Uzoh et al. Sep 2020 B2
10840135 Uzoh Nov 2020 B2
10854578 Morein Dec 2020 B2
10879212 Uzoh et al. Dec 2020 B2
10879226 Uzoh et al. Dec 2020 B2
10886177 DeLaCruz et al. Jan 2021 B2
10892246 Uzoh Jan 2021 B2
10923413 DeLaCruz Feb 2021 B2
10950547 Mohammed et al. Mar 2021 B2
10964664 Mandalapu et al. Mar 2021 B2
10985133 Uzoh Apr 2021 B2
10991804 DeLaCruz et al. Apr 2021 B2
10998292 Lee et al. May 2021 B2
11011503 Wang et al. May 2021 B2
11031285 Katkar et al. Jun 2021 B2
11056348 Theil Jul 2021 B2
11056390 Uzoh et al. Jul 2021 B2
11088099 Katkar et al. Aug 2021 B2
11127738 DeLaCruz et al. Sep 2021 B2
11145623 Hsu et al. Oct 2021 B2
11158606 Gao et al. Oct 2021 B2
11171117 Gao et al. Nov 2021 B2
11176450 Teig et al. Nov 2021 B2
11256004 Haba et al. Feb 2022 B2
11264357 DeLaCruz et al. Mar 2022 B1
11276676 Enquist et al. Mar 2022 B2
11329034 Tao et al. May 2022 B2
11348898 DeLaCruz et al. May 2022 B2
11355443 Huang et al. Jun 2022 B2
11658173 Uzoh et al. May 2023 B2
20020000328 Motomura et al. Jan 2002 A1
20020003307 Suga Jan 2002 A1
20020004288 Nishiyama Jan 2002 A1
20030148591 Guo et al. Aug 2003 A1
20040084414 Sakai et al. May 2004 A1
20040140546 Lee et al. Jul 2004 A1
20040188501 Tolchinsky et al. Sep 2004 A1
20040238927 Miyazawa Dec 2004 A1
20050040530 Shi Feb 2005 A1
20050153522 Hwang et al. Jul 2005 A1
20050161808 Anderson Jul 2005 A1
20060057945 Hsu et al. Mar 2006 A1
20060234473 Wong Oct 2006 A1
20070007639 Fukazawa et al. Jan 2007 A1
20070096294 Ikeda et al. May 2007 A1
20070111386 Kim et al. May 2007 A1
20070123061 Evertsen et al. May 2007 A1
20070158024 Addison et al. Jul 2007 A1
20070222048 Huang Sep 2007 A1
20070295456 Gudeman et al. Dec 2007 A1
20080036082 Eun Feb 2008 A1
20080165521 Bernstein Jul 2008 A1
20080265421 Brunnbauer et al. Oct 2008 A1
20090029274 Olson et al. Jan 2009 A1
20090068831 Enquist et al. Mar 2009 A1
20090095399 Zussy et al. Apr 2009 A1
20090149023 Koyanagi Jun 2009 A1
20090227089 Plaut et al. Sep 2009 A1
20090252939 Park et al. Oct 2009 A1
20090283898 Janzen et al. Nov 2009 A1
20100123268 Menard May 2010 A1
20110042814 Okuyama Feb 2011 A1
20110049696 Haba Mar 2011 A1
20110074033 Kaltalioglu et al. Mar 2011 A1
20110186977 Chi et al. Aug 2011 A1
20110290552 Palmateer et al. Dec 2011 A1
20120003792 Cheah et al. Jan 2012 A1
20120025396 Liao et al. Feb 2012 A1
20120049344 Pagaila et al. Mar 2012 A1
20120077314 Park et al. Mar 2012 A1
20120190187 Yang Jul 2012 A1
20120212384 Kam et al. Aug 2012 A1
20120217644 Pagaila Aug 2012 A1
20120238070 Libbert et al. Sep 2012 A1
20130037962 Xue Feb 2013 A1
20130082399 Kim et al. Apr 2013 A1
20130122655 Yu et al. May 2013 A1
20130169355 Chen et al. Jul 2013 A1
20130299997 Sadaka Nov 2013 A1
20130334697 Shin et al. Dec 2013 A1
20140013606 Nah et al. Jan 2014 A1
20140154839 Ahn et al. Jun 2014 A1
20140175655 Chen Jun 2014 A1
20140187040 Enquist et al. Jul 2014 A1
20140225795 Yu Aug 2014 A1
20140299981 Goh et al. Oct 2014 A1
20140312511 Nakamura Oct 2014 A1
20140327150 Jung et al. Nov 2014 A1
20140370658 Tong et al. Dec 2014 A1
20140377909 Chung et al. Dec 2014 A1
20150021754 Lin et al. Jan 2015 A1
20150048500 Yu et al. Feb 2015 A1
20150064498 Tong Mar 2015 A1
20150097022 Di Cioccio Apr 2015 A1
20150102468 Kang et al. Apr 2015 A1
20150130082 Lu et al. May 2015 A1
20150162294 Kawasaki Jun 2015 A1
20150179481 Lin Jun 2015 A1
20150206865 Yu et al. Jul 2015 A1
20150235949 Yu et al. Aug 2015 A1
20150270209 Woychik et al. Sep 2015 A1
20150303174 Yu et al. Oct 2015 A1
20150340285 Enquest et al. Nov 2015 A1
20160035687 Lin Feb 2016 A1
20160071770 Albermann et al. Mar 2016 A1
20160093592 Zhai Mar 2016 A1
20160141267 Hagimoto May 2016 A1
20160155724 Kim et al. Jun 2016 A1
20160190103 Kabe et al. Jun 2016 A1
20160233175 Dubey et al. Aug 2016 A1
20160300817 Do et al. Oct 2016 A1
20160343682 Kawasaki Nov 2016 A1
20160372323 Doub et al. Dec 2016 A1
20170023405 Fahim et al. Jan 2017 A1
20170148764 Wang et al. May 2017 A1
20170179029 Enquist Jun 2017 A1
20170194271 Hsu et al. Jul 2017 A1
20170200659 Gaynes et al. Jul 2017 A1
20170200711 Uzoh et al. Jul 2017 A1
20170200756 Kao et al. Jul 2017 A1
20170250161 Haba Aug 2017 A1
20170358533 Briggs Dec 2017 A1
20170358553 Kim et al. Dec 2017 A1
20170365591 Chang et al. Dec 2017 A1
20180005992 Yu et al. Jan 2018 A1
20180006006 Kim et al. Jan 2018 A1
20180012787 Oka et al. Jan 2018 A1
20180012863 Yu et al. Jan 2018 A1
20180053746 Yu et al. Feb 2018 A1
20180068958 Cho et al. Mar 2018 A1
20180096931 Huang et al. Apr 2018 A1
20180122774 Huang et al. May 2018 A1
20180130769 Tan et al. May 2018 A1
20180158749 Yu et al. Jun 2018 A1
20180175012 Wu et al. Jun 2018 A1
20180182639 Uzoh et al. Jun 2018 A1
20180182666 Uzoh et al. Jun 2018 A1
20180190580 Haba et al. Jul 2018 A1
20180190583 DeLaCruz et al. Jul 2018 A1
20180219038 Gambino et al. Aug 2018 A1
20180226375 Enquist et al. Aug 2018 A1
20180273377 Katkar et al. Sep 2018 A1
20180286805 Huang et al. Oct 2018 A1
20180323177 Yu et al. Nov 2018 A1
20180323227 Zhang et al. Nov 2018 A1
20180331066 Uzoh et al. Nov 2018 A1
20180366436 Wang Dec 2018 A1
20180366442 Gu et al. Dec 2018 A1
20180366446 Haba et al. Dec 2018 A1
20190096741 Uzoh et al. Mar 2019 A1
20190096842 Fountain, Jr. et al. Mar 2019 A1
20190103409 Xu et al. Apr 2019 A1
20190115277 Yu et al. Apr 2019 A1
20190131277 Yang et al. May 2019 A1
20190157333 Tsai May 2019 A1
20190198407 Huang et al. Jun 2019 A1
20190198409 Katkar et al. Jun 2019 A1
20190265411 Huang et al. Aug 2019 A1
20190319007 Uzoh Oct 2019 A1
20190333550 Fisch Oct 2019 A1
20190333871 Chen et al. Oct 2019 A1
20190341306 Yu et al. Nov 2019 A1
20190348336 Katkar et al. Nov 2019 A1
20190355706 Enquist et al. Nov 2019 A1
20190371763 Agarwal et al. Dec 2019 A1
20190385935 Gao et al. Dec 2019 A1
20190385966 Gao Dec 2019 A1
20200013637 Haba Jan 2020 A1
20200013765 Fountain, Jr. et al. Jan 2020 A1
20200035641 Fountain, Jr. et al. Jan 2020 A1
20200051953 Kurita Feb 2020 A1
20200075520 Gao et al. Mar 2020 A1
20200075534 Gao et al. Mar 2020 A1
20200075553 DeLaCruz et al. Mar 2020 A1
20200098736 Liao Mar 2020 A1
20200106156 Lu Apr 2020 A1
20200118973 Wang et al. Apr 2020 A1
20200126906 Uzoh et al. Apr 2020 A1
20200176419 Dabral et al. Jun 2020 A1
20200194396 Uzoh Jun 2020 A1
20200227367 Haba Jul 2020 A1
20200243380 Uzoh et al. Jul 2020 A1
20200279821 Haba et al. Sep 2020 A1
20200294908 Haba et al. Sep 2020 A1
20200328162 Haba et al. Oct 2020 A1
20200328164 DeLaCruz et al. Oct 2020 A1
20200328165 DeLaCruz et al. Oct 2020 A1
20200335408 Gao et al. Oct 2020 A1
20200371154 DeLaCruz et al. Nov 2020 A1
20200395321 Katkar et al. Dec 2020 A1
20200411483 Uzoh et al. Dec 2020 A1
20210057242 Tang et al. Feb 2021 A1
20210057309 Hu Feb 2021 A1
20210060798 Jeong et al. Mar 2021 A1
20210104487 Uzoh et al. Apr 2021 A1
20210118864 DeLaCruz et al. Apr 2021 A1
20210143125 DeLaCruz et al. May 2021 A1
20210181510 Katkar et al. Jun 2021 A1
20210183847 Uzoh et al. Jun 2021 A1
20210193603 Katkar et al. Jun 2021 A1
20210193624 DeLaCruz et al. Jun 2021 A1
20210193625 DeLaCruz et al. Jun 2021 A1
20210233889 Mandalapu et al. Jul 2021 A1
20210242152 Fountain, Jr. et al. Aug 2021 A1
20210296282 Gao et al. Sep 2021 A1
20210305202 Uzoh et al. Sep 2021 A1
20210366820 Uzoh Nov 2021 A1
20210407941 Haba Dec 2021 A1
20220020729 Gao et al. Jan 2022 A1
20220077063 Haba Mar 2022 A1
20220077087 Haba Mar 2022 A1
20220139867 Uzoh May 2022 A1
20220139869 Gao et al. May 2022 A1
20220189941 Enquist et al. Jun 2022 A1
20220199560 Haba et al. Jun 2022 A1
20220208650 Gao et al. Jun 2022 A1
20220208702 Uzoh Jun 2022 A1
20220208723 Katkar et al. Jun 2022 A1
20220246497 Fountain, Jr. et al. Aug 2022 A1
20220285303 Mirkarimi et al. Sep 2022 A1
20220293567 Uzoh et al. Sep 2022 A1
20220319901 Suwito et al. Oct 2022 A1
20220320035 Uzoh et al. Oct 2022 A1
20220320036 Gao et al. Oct 2022 A1
20230005850 Fountain, Jr. Jan 2023 A1
20230019869 Mirkarimi et al. Jan 2023 A1
20230036441 Haba et al. Feb 2023 A1
20230067677 Lee et al. Mar 2023 A1
20230069183 Haba Mar 2023 A1
20230100032 Haba et al. Mar 2023 A1
20230115122 Uzoh et al. Apr 2023 A1
20230122531 Uzoh Apr 2023 A1
20230123423 Gao et al. Apr 2023 A1
20230125395 Gao et al. Apr 2023 A1
20230130259 Haba et al. Apr 2023 A1
20230130580 Uzoh et al. Apr 2023 A1
20230131849 Uzoh et al. Apr 2023 A1
20230132632 Katkar et al. May 2023 A1
20230140107 Uzoh et al. May 2023 A1
20230142680 Guevara et al. May 2023 A1
20230154816 Haba et al. May 2023 A1
20230154828 Haba et al. May 2023 A1
20230187264 Uzoh et al. Jun 2023 A1
20230187317 Uzoh Jun 2023 A1
20230187412 Gao et al. Jun 2023 A1
20230197453 Fountain, Jr. et al. Jun 2023 A1
20230197496 Theil Jun 2023 A1
20230197559 Haba et al. Jun 2023 A1
20230197560 Katkar et al. Jun 2023 A1
20230197655 Theil et al. Jun 2023 A1
20230207402 Fountain, Jr. et al. Jun 2023 A1
20230207437 Haba Jun 2023 A1
20230207474 Uzoh et al. Jun 2023 A1
20230207514 Gao et al. Jun 2023 A1
20230215836 Haba et al. Jul 2023 A1
20230245950 Haba et al. Aug 2023 A1
20230268300 Uzoh et al. Aug 2023 A1
20230299029 Theil et al. Sep 2023 A1
20230343734 Uzoh et al. Oct 2023 A1
20230360950 Gao Nov 2023 A1
20230361074 Uzoh et al. Nov 2023 A1
20230369136 Uzoh et al. Nov 2023 A1
20230375613 Haba et al. Nov 2023 A1
20240038702 Uzoh Feb 2024 A1
Foreign Referenced Citations (28)
Number Date Country
103681646 Mar 2014 CN
107527885 Dec 2017 CN
2 339 614 Jun 2011 EP
2 685 491 Jan 2014 EP
3 483 925 May 2019 EP
04-337694 Nov 1992 JP
2000-100679 Apr 2000 JP
2001-102479 Apr 2001 JP
2002-353416 Dec 2002 JP
2004-193493 Jul 2004 JP
2009-135348 Jun 2009 JP
2010-073964 Apr 2010 JP
2011-171614 Sep 2011 JP
2013-33786 Feb 2013 JP
2018-160519 Oct 2018 JP
10-2001-0104643 Nov 2001 KR
10-2004-0020827 Mar 2004 KR
10-2010-0123755 Nov 2010 KR
10-2015-0097798 Aug 2015 KR
WO 2005043584 May 2005 WO
WO 2006100444 Sep 2006 WO
WO 2009005898 Jan 2009 WO
WO 2010024678 Mar 2010 WO
WO 2014052445 Apr 2014 WO
WO 2015134227 Sep 2015 WO
WO 2017034654 Mar 2017 WO
WO 2017052652 Mar 2017 WO
WO 2017151442 Sep 2017 WO
Non-Patent Literature Citations (75)
Entry
Frumusanu, Andrei, “TSMC's version of EMIB is ‘LSI’: Currently in pre-qualification,” AnaandTech, https://www.anandtech.com/show/16031/tsmcs-version-of-emib-lsi-3dfabric, Aug. 25, 2020, 6 pages.
Amirfeiz et al., “Formation of silicon structures by plasma-activated wafer bonding,” Journal of The Electrochemical Society, 2000, vol. 147, No. 7, pp. 2693-2698.
Chung et al., “Room temperature GaAseu + Si and InPeu + Si wafer direct bonding by the surface activate bonding method,” Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms, Jan. 2, 1997, vol. 121, Issues 1-4, pp. 203-206.
Chung et al., “Wafer direct bonding of compound semiconductors and silicon at room temperature by the surface activated bonding method,” Applied Surface Science, Jun. 2, 1997, vols. 117-118, pp. 808-812.
Farrens et al., “Chemical free room temperature wafer to wafer direct bonding,” J. Electrochem. Soc., The Electrochemical Society, Inc., Nov. 1995, vol. 142, No. 11. pp. 3949-3955.
Farrens et al., “Chemical free wafer bonding of silicon to glass and sapphire,” Electrochemical Society Proceedings vol. 95-7, 1995, pp. 72-77.
Fukushima, T. et al., “New three-dimensional integration technology using self-assembly technique,” International Electron Devices Meeting Dec. 5-7, 2005, IEEE, Dec. 5, 2005, pp. 348-351.
Gösele et al., “Semiconductor Wafer Bonding: A flexible approach to materials combinations in microelectronics; micromechanics and optoelectronics,” IEEE, 1997, pp. 23-32.
Hosoda et al., “Effect of the surface treatment on the room-temperature bonding of Al to Si and SiO2,” Journal of Materials Science, Jan. 1, 1998, vol. 33, Issue 1, pp. 253-258.
Hosoda et al., “Room temperature GaAs—Si and InP—Si wafer direct bonding by the surface activated bonding method,” Nuclear Inst. And Methods in Physics Research B, 1997, vol. 121, Nos. 1-4, pp. 203-206.
Howlader et al., “A novel method for bonding of ionic wafers,” Electronics Components and Technology Conference, 2006, IEEE, pp. 7-pp.
Howlader et al., “Bonding of p-Si/n-InP wafers through surface activated bonding method at room temperature,” Indium Phosphide and Related Materials, 2001, IEEE International Conference On, pp. 272-275.
Howlader et al., “Characterization of the bonding strength and interface current of p-Si/ n-InP wafers bonded by surface activated bonding method at room temperature,” Journal of Applied Physics, Mar. 1, 2002, vol. 91, No. 5, pp. 3062-3066.
Howlader et al., “Investigation of the bonding strength and interface current of p-SionGaAs wafers bonded by surface activated bonding at room temperature,” J. Vac. Sci. Technol. B 19, Nov./Dec. 2001, pp. 2114-2118.
International Search Report and Written Opinion mailed Apr. 17, 2017, issued in International Application No. PCT/US2016/068577, 16 pages.
International Search Report and Written Opinion mailed Sep. 22, 2017, issued in International Application No. PCT/US2017/029187, 20 pages.
International Search Report and Written Opinion mailed Mar. 7, 2019, in International Application No. PCT/US2018/060044, 14 pages.
International Search Report and Written Opinion mailed Apr. 22, 2019 in International Application No. PCT/US2018/064982, 13 pages.
International Search Report and Written Opinion mailed Oct. 25, 2019, issued in International Application No. PCT/US2019/040622, 12 pages.
Itoh et al., “Characteristics of fritting contacts utilized for micromachined wafer probe cards,” 2000 American Institute of Physics, AIP Review of Scientific Instruments, vol. 71, 2000, pp. 2224.
Itoh et al., “Characteristics of low force contact process for MEMS probe cards,” Sensors and Actuators A: Physical, Apr. 1, 2002, vols. 97-98, pp. 462-467.
Itoh et al., “Development of MEMS IC probe card utilizing fritting contact,” Initiatives of Precision Engineering at the Beginning of a Millennium: 10th International Conference on Precision Engineering (ICPE) Jul. 18-20, 2001, Yokohama, Japan, 2002, Book Part 1, pp. 314-318.
Itoh et al., “Room temperature vacuum sealing using surface activated bonding method,” The 12th International Conference on Solid State Sensors, Actuators and Microsystems, Boston, Jun. 8-12, 2003, 2003 IEEE, pp. 1828-1831.
Ker, Ming-Dou et al., “Fully process-compatible layout design on bond pad to improve wire bond reliability in CMOS Ics,” IEEE Transactions on Components and Packaging Technologies, Jun. 2002, vol. 25, No. 2, pp. 309-316.
Kim et al., “Low temperature direct Cu—Cu bonding with low energy ion activation method,” Electronic Materials and Packaging, 2001, IEEE, pp. 193-195.
Kim et al., “Room temperature Cu-Cu direct bonding using surface activated bonding method,” J. Vac. Sci. Technol., 2003 American Vacuum Society, Mar./Apr. 2003, vol. 21, No. 2, pp. 449-453.
Kim et al., “Wafer-scale activated bonding of Cu—CU, Cu—Si, and Cu—SiO2 at low temperature,” Proceedings—Electrochemical Society, 2003, vol. 19, pp. 239-247.
Matsuzawa et al., “Room-temperature interconnection of electroplated Au microbump by means of surface activated bonding method,” Electornic Components and Technology Confererence, 2001, 51st Proceedings, IEEE, pp. 384-387.
Moriceau, H. et al., “Overview of recent direct wafer bonding advances and applications,” Advances in Natural Sciences-Nanoscience and Nanotechnology, 2010, 11 pages.
Nakanishi, H. et al., “Studies on SiO2—SiO2 bonding with hydrofluoric acid. Room temperature and low stress bonding technique for MEMS,” Sensors and Actuators, 2000, vol. 79, pp. 237-244.
Oberhammer, J. et al., “Sealing of adhesive bonded devices on wafer level,” Sensors and Actuators A, 2004, vol. 110, No. 1-3, pp. 407-412, see pp. 407-412, and Figures 1(a)-1(I), 6 pages.
Onodera et al., “The effect of prebonding heat treatment on the separability of Au wire from Ag-plated Cu alloy substrate,” Electronics Packaging Manufacturing, IEEE Transactions, Jan. 2002, vol. 25, Issue 1, pp. 5-12.
Plobi, A. et al., “Wafer direct bonding: tailoring adhesion between brittle materials,” Materials Science and Engineering Review Journal, 1999, R25, 88 pages.
Reiche et al., “The effect of a plasma pretreatment on the Si/Si bonding behaviouir,” Electrochemical Society Proceedings, 1998, vol. 97-36, pp. 437-444.
Roberds et al., “Low temperature , in situ, plasma activated wafer bonding,” Electrochecmical Society Proceedings, 1997, vol. 97-36, pp. 598-606.
Shigetou et al., “Room temperature bonding of ultra-fine pitch and low-profiled Cu electrodes for bump-less interconnect,” 2003 Electronic Components and Technology Conference, pp. 848-852.
Shigetou et al., “Room-temperature direct bonding of CMP-Cu film for bumpless interconnection,” Electronic Components and Technology Confererence, 51st Proceedings, 2001, IEEE, pp. 755-760.
Shingo et al., “Design and fabrication of an electrostatically actuated MEMS probe card,” Tranducers, Solid-State Sensors, Actuators and Microsystems, 12th International Conference, Jun. 8-12, 2003, vol. 2, pp. 1522-1525.
Suga et al., “A new approach to Cu—Cu direct bump bonding,” IEMT/IMC Symposium, 1997, Joint International Electronic Manufacturing Symposium and the International Microelectronics Conference, Apr. 16-18, 1997, IEEE, pp. 146-151.
Suga et al., “A new bumping process using lead-free solder paste,” Electronics Packaging Manufacturing, IEEE Transactions on (vol. 25, Issue 4), IEEE, Oct. 2002, pp. 253-256.
Suga et al., “A new wafer-bonder of ultra-high precision using surface activated bonding (SAB) concept,” Electronic Components and Technology Conference, 2001, IEEE, pp. 1013-1018.
Suga et al., “Bump-less interconnect for next generation system packaging,” Electronic Components and Technology Conference, 2001, IEEE, pp. 1003-1008.
Suga, T., “Feasibility of surface activated bonding for ultra-fine pitch interconnection—A new concept of bump-less direct bonding for system level packaging,” The University of Tokyo, Research Center for Science and Technology, 2000 Electronic Components and Technology Conference, 2000 IEEE, pp. 702-705.
Suga, T., “Room-temperature bonding on metals and ceramics,” Proceedings of the Second International Symposium on Semiconductor Wafer Bonding: Science, Technology and Applications, The Electrochemical Society Proceedings, vol. 93-29 (1993), pp. 71-80.
Suga et al., “Surface activated bonding—an approach to joining at room temperature,” Ceramic Transactions: Structural Ceramics Joining II, The American Ceramic Society, 1993, pp. 323-331.
Suga et al., “Surface activated bonding for new flip chip and bumpless interconnect systems,” Electronic Components and Technology Conference, 2002, IEEE, pp. 105-111.
Suga, “UHV room temperature joining by the surface activated bonding method,” Advances in science and technology, Techna, Faenza, Italie, 1999, pp. C1079-C1089.
Takagi et al., “Effect of surface roughness on room-temperature wafer bonding by Ar beam surface activation,” Japanese Journal of Applied Physics, 1998, vol. 37, Part 1, No. 1, pp. 4197.
Takagi et al., “Low temperature direct bonding of silicon and silicon dioxide by the surface activation method,” Solid State Sensors and Actuators, 1997, Transducers '97 Chicago, 1997 International Conference, vol. 1, pp. 657-660.
Takagi et al., “Room-temperature bonding of lithium niobate and silicon wafers by argon-beam surface activation,” Appl. Phys. Lett., 1999. vol. 74, pp. 2387.
Takagi et al., “Room temperature silicon wafer direct bonding in vacuum by Ar beam irradiation,” Micro Electro Mehcanical Systems, MEMS '97 Proceedings, 1997, IEEE, pp. 191-196.
Takagi et al., “Room-temperature wafer bonding of Si to LiNbO3, LiTaO3 and Gd3Ga5O12 by Ar-beam surface activation,” Journal of Micromechanics and Microengineering, 2001, vol. 11, No. 4, pp. 348.
Takagi et al., “Room-temperature wafer bonding of silicon and lithium niobate by means of arbon-beam surface activation,” Integrated Ferroelectrics: An International Journal, 2002, vol. 50, Issue 1, pp. 53-59.
Takagi et al., “Surface activated bonding silicon wafers at room temperature,” Appl. Phys. Lett. 68, 2222 (1996).
Takagi et al, “Wafer-scale room-temperature bonding between silicon and ceramic wafers by means of argon-beam surface activation,” Micro Electro Mechanical Systems, 2001, MEMS 2001, The 14th IEEE International Conference, Jan. 25, 2001, IEEE, pp. 60-63.
Takagi et al., “Wafer-scale spontaneous bonding of silicon wafers by argon-beam surface activation at room temperature,” Sensors and Actuators A: Physical, Jun. 15, 2003, vol. 105, Issue 1, pp. 98-102.
Tong et al., “Low temperature wafer direct bonding,” Journal of Microelectomechanical systems, Mar. 1994, vol. 3, No. 1, pp. 29-35.
Topol et al., “Enabling technologies for wafer-level bonding of 3D MEMS and integrated circuit structures,” 2004 Electronics Components and Technology Conference, 2004 IEEE, pp. 931-938.
Uhrmann, T. et al., “Heterogeneous integration by collective die-to-wafer bonding,” Chip Scale Review, Nov./Dec. 2018, vol. 22, No. 6, pp. 10-12.
Wang et al., “Reliability and microstructure of Au—Al and Au—Cu direct bonding fabricated by the Surface Activated Bonding,” Electronic Components and Technology Conference, 2002, IEEE, pp. 915-919.
Wang et al., “Reliability of Au bump—Cu direct interconnections fabricated by means of surface activated bonding method,” Microelectronics Reliability, May 2003, vol. 43, Issue 5, pp. 751-756.
Weldon et al., “Physics and chemistry of silicon wafer bonding investigated by infrared absorption spectroscopy,” Journal of Vacuum Science & Technology B, July/Aug. 1996, vol. 14, No. 4, pp. 3095-3106.
Xu et al., “New Au—Al interconnect technology and its reliability by surface activated bonding,” Electronic Packaging Technology Proceedings, Oct. 28-30, 2003, Shanghai, China, pp. 479-483.
Ceramic Microstructures: Control at the Atomic Level, Recent Progress in Surface Activated Bonding, 1998, pp. 385-389.
Bush, Steve, “Electronica: Automotive power modules from On Semi,” ElectronicsWeekly.com, indicating an ONSEMI AR0820 product was to be demonstrated at a Nov. 2018 trade show, https://www.electronicsweekly.com/news/products/power-supplies/electronica-automotive-power-modules-semi-2018-11/ (published Nov. 8, 2018; downloaded Jul. 26, 2023).
Chang, T.C. et al., “A method for fabricating a superior oxide/nitride/oxide gate stack,” Electrochemical and Solid-State Letters, 2004, vol. 7, No. 7, pp. G138-G140.
“Die-to-Wafer Fusion and Hybrid Bonding,” EV Group, https://www.evgroup.com/technologies/die-to-wafer-fusion-and-hybrid-bonding/, printed Sep. 21, 2022, 8 pages.
Gao, G. et al., “Low temperature hybrid bonding for die to wafer stacking applications,” 2021 IEEE 71st Electronic Components and Technology Conference (ECTC), IEEE, Jun. 1, 2021-Jul. 4, 2021.
Hooper, A. et al. “Review of wafer dicing techniques for via-middle process 3DI/TSV ultrathin silicon device wafers,” 2015 IEEE 65th Electronic Components and Technology Conference (ECTC).
Jin, H. et al., “Silicon / Silicon Oxide / LPCVD Silicon Nitride Stacks: The Effect of Oxide Thickness on Bulk Damage and Surface Passivation,” Centre for Sustainable Energy Systems, Faculty of Engineering and Information Technology, The Australian National University, Canberra ACT 0200, Australia, 3 pages.
“Lecture 29: Productivity and process yield,” National Programme on Technology Enhanced Learning (NPTEL), MM5017: Electronic materials, devices, and fabrication, 16 pages.
Morrison, Jim et al., “Samsung Galaxy S7 Edge Teardown,” Tech Insights (posted Apr. 24, 2016), includes description of hybrid bonded Sony IMX260 dual-pixel sensor, https://www.techinsights.com/blog/samsung-galaxy-s7-edge-teardown, downloaded Jul. 11, 2023, 9 pages.
ONSEMI AR0820 image, cross section of a CMOS image sensor product. The part in the image was shipped on Sep. 16, 2021. Applicant makes no representation that the part in the image is identical to the part identified in the separately submitted reference Bush, Nov. 8, 2018, ElectronicsWeekly.com (“Bush article”); however, the imaged part and the part shown in the Bush article share the part number “ONSEMI AR0820.”.
Sony IMX260 image, cross section of Sony dual-pixel sensor product labeled IMX260, showing peripheral probe and wire bond pads in a bonded structure. The part in the image was shipped in Apr. 2016. Applicant makes no representation that the part in the image is identical to the part identified in the separately submitted reference Morrison et al. (Tech Insights article dated Apr. 24, 2016), describing and showing a similar sensor product within the Samsung Galaxy S7; however the imaged part and the part shown in the Morrison et al. article share the part name “Sony IMX260.”.
“The effects of edge trimming—Engineering R&D Division, Operation V,” Disco Technical Review Mar. 2016, 3 pages.
Related Publications (1)
Number Date Country
20210098412 A1 Apr 2021 US
Provisional Applications (1)
Number Date Country
62906608 Sep 2019 US