Nanowire bonding interconnect for fine-pitch microelectronics

Information

  • Patent Grant
  • 12191267
  • Patent Number
    12,191,267
  • Date Filed
    Monday, July 11, 2022
    2 years ago
  • Date Issued
    Tuesday, January 7, 2025
    a month ago
Abstract
A nanowire bonding interconnect for fine-pitch microelectronics is provided. Vertical nanowires created on conductive pads provide a debris-tolerant bonding layer for making direct metal bonds between opposing pads or vias. Nanowires may be grown from a nanoporous medium with a height between 200-1000 nanometers and a height-to-diameter aspect ratio that enables the nanowires to partially collapse against the opposing conductive pads, creating contact pressure for nanowires to direct-bond to opposing pads. Nanowires may have diameters less than 200 nanometers and spacing less than 1 μm from each other to enable contact or direct-bonding between pads and vias with diameters under 5 μm at very fine pitch. The nanowire bonding interconnects may be used with or without tinning, solders, or adhesives. A nanowire forming technique creates a nanoporous layer on conductive pads, creates nanowires within pores of the nanoporous layer, and removes at least part of the nanoporous layer to reveal a layer of nanowires less than 1 μm in height for direct bonding.
Description
BACKGROUND

As microelectronic devices decrease in size, the pitch of line-space patterning for conductive leads and traces in the devices also decreases. Techniques such as direct bond interconnect (DBI®) direct hybrid bonding have been invented to make reliable electrical interconnects at smaller and smaller scales (Ziptronix Inc., a subsidiary of Xperi Corporation, San Jose, CA). Such DBI techniques can accomplish a million separate solderless electrical couplings per square millimeter, under ideal circumstances. Such high joining density calls for careful fabrication conditions and ultra-flat surfaces that are extremely clean. Viable alternatives to DBI direct hybrid bonding techniques for making fine-pitch conductive connections on pads less than 5 μm across are rare, especially when conditions are less than ideal. There is interest in finding new bonding techniques that can make high-density ultra-fine pitch interconnects during fabrication and 3D-packaging of microelectronic devices.


SUMMARY

A nanowire bonding interconnect for fine-pitch microelectronics is provided. Vertical nanowire pins or posts created on conductive pads provide a debris-tolerant bonding layer for making direct metal-to-metal bonds with opposing conductive pads or opposing vias. Nanowires may be grown from a nanoporous medium with a height between approximately 200-1000 nanometers (0.2-1.0 μm) and a height-to-diameter aspect ratio that enables the nanowires to partially collapse against the opposing conductive pads, thereby providing spring compression of the nanowires and contact pressure for conductive contact or direct metallic-bonding to the opposing pads. Nanowires may have diameters less than 200 nanometers and spacing less than 1 μm between each other to enable direct-metallic bonding for pads and vias with diameters under 5 μm, arrayed at very fine pitch. The nanowire bonding interconnects may be used with or without tinning, solders, or adhesives. A nanowire forming technique creates a nanoporous layer on conductive pads or across an entire surface, creates nanowires within pores of the nanoporous layer, and then removes all or at least part of the nanoporous layer to reveal a nanowire bonding layer that may be less than 1 μm in vertical height for direct metallic-bonding between opposing pads or between opposing vias.


This summary is not intended to identify key or essential features of the claimed subject matter, nor is it intended to be used as an aid in limiting the scope of the claimed subject matter.





BRIEF DESCRIPTION OF THE DRAWINGS

Certain embodiments of the disclosure will hereafter be described with reference to the accompanying drawings, wherein like reference numerals denote like elements. It should be understood, however, that the accompanying figures illustrate the various implementations described herein and are not meant to limit the scope of various technologies described herein.



FIG. 1 is a diagram of an example nanowire bonding interface formed on conductive pads of a surface to be bonded.



FIG. 2 is a diagram of an example nanowire bonding interface formed across an entire surface to be bonded.



FIG. 3 is a diagram of an example nanowire bonding interface formed on through-silicon-vias (TSVs) at a surface to be bonded.



FIG. 4 is a diagram of example extra dummy bonding pads on surfaces to be bonded across a nanowire bonding interface.



FIG. 5 is a diagram of example nanowires embedded directly in a chip substrate for making a nanowire bonding interface.



FIG. 6 is a diagram of an example nanowire bonding interface in which the nanporous layer used to form the nanowires has been removed after the nanowires are formed.



FIG. 7 is a diagram of example nanowires before and after bonding with an opposing pad.



FIG. 8 is a diagram of example nanowires before and after bonding with an opposing pad in the presence of an adhesive.



FIG. 9 is a diagram of example nanowires before and after bonding with an opposing pad, in the presence of an adhesive and a solder or flowable joining metal or material.



FIG. 10 is a diagram of an example nanowire bonding interface with an adhesive layer placed across an entire area of the surface to be bonded.



FIG. 11 is a diagram of an example process of fabricating a nanowire bonding interface.



FIG. 12 is a diagram of an example process of creating nanowires through a combination lithography process.



FIG. 13 is a diagram of another example process of creating nanowires through a combination lithography process.



FIG. 14 is a diagram of a flowable joining material or solder applied to the nanowires of a nanowire bonding interface.



FIG. 15 is a diagram of an example planarized nanowire bonding interface.



FIG. 16 is a diagram of additional nanowire growth on a planarized nanowire bonding interface.



FIG. 17 is a diagram of an example two-sided interposer with nanowire bonding interfaces on each side.



FIG. 18 is a flow diagram of an example method of fabricating an example nanowire bonding interface.





DESCRIPTION
Overview

This disclosure describes a nanowire bonding interconnect for fine-pitch microelectronics. In an implementation, vertical nanowire pins or posts are created on conductive pads of a microelectronics device, or on an entire surface of a chip, wafer, or device to provide a thin debris-tolerant bonding layer that can form interconnects between conductive pads that are less than 5 μm across and laid out at fine-pitch, even in the presence of trace amounts of tiny debris particles. The nanowire bonding interface described herein can be used under ideal conditions, but can also be used in some circumstances when conductive pads or leads to be bonded together are not ideal candidates for conventional direct bonding, due to lesser quality of the conductive surfaces being bonded, variance in the flatness needed for direct bonding, or imperfect surface preparation for conventional direct bonding techniques.


Nanowires with a diameter less than 200 nanometers (nm) and a horizontal spacing from each other of 1 μm or less enable conductive contact or direct metal-to-metal bonding between pads that have dimensions under 5 μm and comparable line and pitch (spacing) distances. The small diameter of the nanowires at 200 nm or less enables conductive pads much smaller than 5 μm to still have at least 3-4 nanowires 100 on their surface. The nanowires may be grown from a nanoporous medium with a height between approximately 200-1000 nanometers, for example, and a height-to-diameter aspect ratio that enables the nanowires to partially collapse against the opposing conductive pads under applied pressure, thereby providing a desirable compression of the nanowires and contact pressure for making electrical interconnects and for direct metal-to-metal bonding of the nanowires to the opposing conductive pads or vias. The nanowire bonding interconnects may be used to join surfaces with or without tinning, solders, or adhesives, depending on implementation. Some embodiments use flowable joining materials, solder, or an adhesive to join devices, dies, or surfaces on either side of the vertically disposed nanowires.


The nanowire bonding layer can be implemented on conductive pads only, or can be implemented on an entire surface of a semiconductor wafer, silicon substrate, semiconductor die, chip, package, assembly, dielectric, or even just on a surface that has electrical contacts. The nanowire bonding layer can also be embodied in a two-sided interposer that can bond chips and wafers on both sides of the two-sided interposer.


Techniques for forming the nanowire bonding interface are also described. An example method creates a nanoporous layer of a nonmetal, for example, on each conductive pad of a surface to be bonded. Nanowires are plated, deposited, or otherwise formed within the pores of the nanoporous layer, and then at least a part of the nanoporous layer may be removed, or recessed, to reveal a layer of bondable nanowire ends that may be less than 1 μm in height for direct metallic-bonding between opposing pads or between opposing vias, in one example process.


Dimensions of the nanowires for their diameter and height may be selected so that a pressure force needed to electrically interconnect two opposing pads and collapse the nanowires into a slightly compressed state is less than the yielding force of the same bulk materials used.


Example Bonding Interfaces

Dimensions of members and elements shown in the Figures are not to scale and not in proportion relative to each other, but are shown in a manner that aids in understanding the description of features.



FIG. 1 shows example nanowires 100 (“pins” or “posts”) making up an example nanowire bonding interface 102. The nanowire bonding interface 102 may be used to make a microelectronics package 104 that includes a die-to-die, die-to-wafer, or wafer-to-wafer interface between two components of the microelectronic package 104. The nanowires 100 are grown from a nanoporous medium 106, for example made of a dielectric material, and may be formed or grown only on conductive pads 108 to be bonded, or may be formed across the entire surface to be bonded or joined. In an implementation, the nanowires 100 may be grown on conductive pads 108 on opposing surfaces to be bonded, and the nanowires 100 on each side bond to the conductive pads 108 and nanowires 100 on the opposing side of the bond.


The nanowires 100 can be made of copper, nickel, aluminum, silver, tungsten, alloy, or another suitable electrical conductor. The nanowires 100 can also be covered, coated, alloyed, or amalgamated with other metals, such as gold or other metals attractive for bonding, soldering, or making a multi-metal intermetallic bonding interface between conductors that are being joined into an interconnect.


In an implementation, formation of the nanowires 100 uses a nanoporous film or layer 106. This nanoporous starting layer 106 can be made of porous silicon, oxidized alumina, silicon dioxide, ceramic, or a host of other materials, such as various dielectric materials. Moreover, the nanoporous starting layer 106 does not need to be porous from the outset. A suitable material is applied to the chip, wafer, or other surface, and the pores can be created by various techniques, such as electrochemical etching, chemical vapor deposition, sputtering, alkali corrosion, and many other processes for creating nanoporous films and surfaces.


In an implementation, the nanowires 100 are formed, plated, deposited, or grown in the pores of the nanoporous layer 106. This formation process may include depositing a film of insulator material on the walls of the pores, in the event that the nanoporous layer 106 itself is conductive, or is semiconductive, as in the case of silicon. The nanowire formation process may also include cleaning the bottom of the pores, in order for the nanowires 100 being created to make electrical contact with the conductive pads underlying the nanoporous layer 106. Once nanowires 100 of a desired vertical height are formed, the nanoporous layer 106 may be partially or completely removed, or recessed, providing “free” ends of the nanowires 100 for bonding with an opposing conductive pad 108, or another opposing instance of the nanowire bonding interface 102, on the opposing side of the bond. The nanowires 100 can be made any height or length, but a useful height in one example implementation is between approximately 200-1000 nanometers (e.g., up to 1 μm). The free ends of the nanowires 100 can make conductive contact via simple physical contact or by direct metal bonding of the ends to a conductive surface. Optionally a flowable joining material such as a solder may be used. In an implementation, the nanowires 100 can be held in contact with permanent adhesive that is placed elsewhere on the surfaces being joined away from the nanowires 100, or in an implementation, the adhesive may be mixed in with the nanowires 100 in areas where the nanowires 100 make electrical contact with an opposing pad 108. The nanowires 100 may bend, kink, and/or conform to small debris particles, leaving the remaining nanowires 100 to bond. The bonding nanowires 100 compress to a degree, provide some contact pressure against the opposing pad 108 for electrical contact and for direct metal bonding.


The completed nanowire bonding interface 102, including both the nanowires 100 and the nanoporous layer 106, may sometimes be only 1 μm or less in vertical height. This height, or a similar height, is enough to provide a more forgiving bonding approach when micro-particles are present than conventional surface-to-surface direct bonding, which uses ultra-flat and ultra-clean prepared bonding surfaces that are flatly planar.


In an implementation, since the nanowires 100, on average, are only about 1 μm apart from each other horizontally, and sometimes much less, the nanowire bonding interface 102 can form interconnects at pitches much smaller than 5 μm.



FIG. 2 shows an implementation of the nanowire bonding interface 102, in which nanowires 100 and a nanoporous layer 106 have been created on an entire surface 200 to be bonded. Coating an entire surface 200 with the nanowires 100 can sometimes be easier than the scenario of FIG. 1, in which the nanowires 100 are only grown on conductors 108 that make an electrical interconnect between conductive pads on opposing surfaces being joined. Coating an entire surface with the nanowires 100, as in FIG. 2, can also be used to make stronger cumulative bonds between two surfaces being joined, and can allow full physical bonding between surfaces, even with conductive pads that have some vertical misalignment with respect to their electrical interconnection.



FIG. 3 shows example nanowires 100 formed on pads 108, on through-silicon-vias (TSVs) 302, or on both pads 108 and TSVs 302. Moreover, the TSVs 302 can also be outfitted with TSV pads 304 of their own, at the bonding interface. Nanowires 100 that do not connect vertically with an opposing pad 108, TSV 302, or opposing TSV pad 304 merely kink, bend, collapse, or break against an opposing surface of insulator or dielectric.



FIG. 4 shows an example implementation in which additional metal pads 402 that are not necessarily involved in circuitry or conductive connection can be designed onto a surface, horizontally between the conductive pads 108 in order to form a stronger vertical bond between surfaces being joined, using the nanowires 100 at both types of pads, pads 108 and pads 402. The extra “dummy” pads 402 may also be used for heat-sinking, as the nanowires 100 are excellent conduits for flowing thermal energy generated by an integrated circuit of a die or heat generated within the larger microelectronics package 104 to a heat sink or to a dissipating structure.



FIG. 5 shows another implementation of an example bonding interface, in which the nanowires 100 are formed or “embedded” 502 in a surface 500 of the die itself, with no extra nanoporous layer 106 added in the nanowire 100 formation process. This can be accomplished by performing one of the nanopore-creating techniques described above, directly on the silicon semiconductor material or on a substrate material of a die, wafer, or other surface. A layer of adhesive 504 that has less height than the vertical height of the nanowires 100 may be added for joining the surfaces together. The joining may be made under pressure, so that the nanowires 100 can contact opposing pads 108 under some compression and contact pressure, while the adhesive 504 sets or hardens, making the contact between nanowires 100 and the contact pads 108 permanent.



FIG. 6 shows an implementation of the nanowire bonding interface 102 in which the nanoporous layer 106 used to form the nanowires 100 has been removed after the nanowires 100 are formed. This configuration allows the metal of the nanowires 100 to direct-bond with the same metal used in an opposing contact pad 108, with no other material between conductive pads 108 besides the nanowires 100, and air. Such direct metal bonds make the electrical interconnects between conductive pads 108 and can also provide the physical joining bond or mechanical connection between the two surfaces, such as between dies, or between die and wafer. In implementations where the nanoporous layer 106 is to be removed, a removable material is used. Removal of the nanoporous layer 106 depends on what substance is used as the nanoporous layer 106. A masking material, or other etchable material can be used, such as an organic photoresist, silicon, or silicon dioxide, for example. Chemical, photo, or plasma etching may be used, depending on material, leaving the nanowires 100 freestanding, although only approximately a micron in height. Some forms of alumina (aluminum oxide) can be made removable. In this implementation, the joined package 602 has no remaining nanoporous layer 106 (FIG. 1).



FIG. 7 shows the nanowires 100 before and after bonding with an opposing pad 702. When the conductive pads 108 & 702 are small, such as less than 5 μm in length or diameter, then each pad 108 & 702 may still have 2-4 nanowires 100, since the nanowires 100 may have a diameter of 200 nm, and a spacing of less than 1 μm, with the average height of the nanowires 100 approximately 1 μm or less. The two surfaces to be joined are brought together with enough pressure to press the nanowires 100 down to a common level of the lowest nanowires 100 in vertical height. The nanowires 100 may vary in height between 5-10%. When pressed, the nanowires 100 collapse slightly under the compression. This compressed state gives the nanowires 100 a measure of springlike contact pressure against the opposing conductive pad 702. This implementation may be used with (FIG. 8) or without an adhesive that makes the join permanent, including the compressed nanowires 100. The compressed nanowires 100 with their contact pressure against the opposing conductive pad 702 may form their own direct metal-to-metal bonds with the opposing conductive pad 702. The two surfaces may be held together by the direct bonds formed between the nanowires 100 and the opposing conductive pad 702, or alternatively or in addition the surfaces may be held together by mechanical force or by an adhesive (as in FIG. 8).



FIG. 8 shows the nanowires 100 before and after bonding with an opposing pad 802. In this implementation, the joining is made permanent with an adhesive 804. The height of the shortest nanowire 100 should be greater in height over the top dielectric surface of its die or wafer than the thickness of the dielectric or adhesive 804 layer on the opposing chip, in order for the nanowire 100 to reach the opposing conductive pad 802. Overall, the average height of the nanowires 100 may be approximately 1 μm or less. The conductive pads 108 & 802 on each side of the join may be horizontally smaller than 5 μm in length or diameter, but each pad 108 & 802 still has at least several of the nanowires 100, since the nanowires 100 can have diameters of 200 nm or less, and a spacing of 1 μm or less from each other. The two surfaces to be joined are brought together with pressure enough to compress the nanowires 100 down to a level of the lowest nanowires 100 in vertical height. The nanowires 100 may vary in height between 5-10%. When pressured, the nanowires 100 compress slightly under the pressure. This compressed state provides contact pressure for the nanowires 100 against the opposing conductive pad 802. In FIG. 8, the adhesive 804 is placed only between areas of both surfaces that do have nanowires 100 to be bonded. The adhesive 804 then sets or hardens under compression, fixing the nanowires 100 against the opposing conductive pad 802 in their compressed state. The nanowires 100 may make direct metal-to-metal bonds in their own right, with the opposing contact pad 802, regardless of the adhesive 804 holding the surfaces together.



FIG. 9 shows the nanowires 100 before and after bonding with an opposing pad 902, with both adhesive 904 and a flowable joining material such as solder 906 present. The height of the smallest nanowire 100 should be higher above than the top dielectric surface of its die or wafer than the height or thickness of the dielectric, adhesive 904, or solder layer 906 on the opposing surface, in order to reach the opposing conductive pad 902. The average height of the nanowires 100 may be approximately 1 μm or less. The conductive pads 108 & 902 on each side of the join may be smaller than 5 μm, but each pad 108 & 902 still has at least several of the nanowires 100, since the nanowires 100 are small too, with diameters less than 200 nm, and a spacing of approximately 1 μm or less from each other.


The two surfaces to be joined are brought together with pressure enough to penetrate the nanowires 100 through the solder layer 906 or other flowable joining material and to compress the nanowires 100 down to a level of the tops of the lowest nanowires 100 in vertical height. If the temperature is to be raised as part of the specific process, then the solder 906 or other joining metal flows over the nanowires 100, and optionally over the pad 108 beneath the nanowires 100. The nanowires 100 may vary in height between 5-10%. When pressured, the nanowires 100 compress slightly under the pressure. This compressed state provides contact pressure for the nanowires 100 against the opposing conductive pad 902. The adhesive 904 may be placed only between areas of both surfaces that do have nanowires 100 to be bonded. The adhesive 904 then sets or hardens under compression, fixing the nanowires 100 against the opposing conductive pad 902 in their compressed state.


The nanowires 100 may make direct metal-to-metal bonds in their own right, with the opposing contact pad 902, regardless of the adhesive 904 holding the surfaces together. The compressed nanowires 100 and their contact pressure against the opposing conductive pad 902 may be made solid with the solder 906, or with a nickel-solder interface, when the solder 906 or other flowable joining material is mixed with the nanowires 100, or placed as a layer on top of the nanowires 100, or placed on the opposing chip, die, or wafer. Other flowable joining materials and combinations of flowable joining materials may also be used.


For nanowire bonding interfaces that include a solder 906, the nanowires 100 may penetrate the malleable solder and may enter into the metal-metal bond formed by the solder and the conductive pad 902 being bonded, while the nanowires 100 horizontally outside the confines of the conductive pads 902 merely conform to the non-metal part of the surface by yielding, including bending, kinking, or breaking. The yielding nanowires 100 up against a nonmetal do not enter into formation of an electrical interconnect.


In an example joining process, the opposing surfaces are aligned until the nanowires 100 touch the opposing conductive pads 902, the temperature is raised, optionally until the joining metal flows, then the backs of the two chips, dies, or wafers are pressed until the adhesive 904 joins the top dielectric surfaces of the chips, dies, or wafers.



FIG. 10 shows an example nanowire bonding interface with nanowires 100 to be bonded to an opposing conductive pad 1002. An adhesive layer 1004 is placed across an entire area of the surface to be bonded, including in the areas of the nanowires 100 and likewise over areas that have no nanowires 100. The adhesive layer 1004 is of lesser height than the average height of the nanowires 100, so that the ends of the nanowires 100 may contact the opposing conductive pads 1002 without much interference of the adhesive layer 1004, and to prevent an excess volume of the adhesive 1004 interfering with the joining. The adhesive layer 1004 may initially be placed on the same surface as the nanowires 100, or may be placed on the opposing surface, as shown.



FIG. 11 shows an example fabrication process 1100 in steps. In one implementation of a fabrication process, a thin layer 1102 of a material is deposited on a surface of a die, wafer, or substrate, including upon conductive areas that are to become one or more conductive interconnects. If TSVs are present, then a conductive surface of each TSV is exposed, from the back of the wafer, for example. Pads, such as pads 304 in FIG. 3, may be added to the surface aspect of TSVs 302, if needed.


Pores 1104 are then formed in the deposited material 1102, if the deposited material 1102 is not already nanoporous. If needed, a film of insulator material 1106 is deposited on the walls of the pores 1104, when the deposited material 1102 is a conductor or semiconductor.


Also, if needed, the bottoms 1108 of the pores 1104 are then cleaned as needed, to prepare for good electrical conduction between pads 108 and the conductive nanowires 100 to be formed next.


Next, the pores 1104 are plated or otherwise filled with a metal, such as copper to make the nanowires 100. The nanowires 100 may be formed by deposition, electrolytic plating, electroless plating, crystal growth, and so forth. The nanowires 100 may be grown to an average height, and then planarized if desired to average heights that are within 5-10% of each other. If greater uniformity of height is desired than is present after nanowire growth, the nanowires may be lapped, for example, and ends further plated on the nanowires 100 by electroless plating or other techniques.


Next, the nanoporous layer 1102 may be at least partially removed 1110 or recessed 1110 to expose at least some of the vertical length of the nanowires 100, for bonding, if such ends are not already exposed. The nanoporous layer 1102 may be recessed or removed by chemical means, electrochemical means, or physical means, depending on the material 1102 used.



FIG. 12 shows an example process of creating nanowires 100 through a combination lithography process. A chip, die, or wafer 1200 has conductive traces 1202, onto which a film of polymer 1204 or other material is spread for becoming a nanoporous layer for creating the nanowires 100. The polymer 1204 may be baked, if needed.


A seed layer 1206 of a first metal is deposited over conductors or pads where the nanowires 100 are to be present for bonding to an opposing conductive pad on another surface.


A photoresist layer 1208 is deposited over the seed layer 1206 and over the polymer layer 1204. Photolithography of the photoresist layer 1208 makes nanopores 1210 in the photoresist layer 1208. Alternatively, the photoresist layer 1208 is just a resist that is etched in another manner to make the nanopores 1210, without light. The nanopores may be 200 nm in diameter, or smaller.


Copper metal, or another metal, is plated or otherwise grown on the seed layer 1206, forming the nanowires 100. In an implementation, the metal plated or deposited as the nanowires 100 is a different metal than the first metal of the seed layer 1206. This is to provide selectivity for stripping or cleaning the copper metal or other metal used for the nanowires 100, so that the stripping or cleaning does not remove the attachment of the nanowires 100 from their seed layer 1206, which should be impervious to the stripper or cleaner.


The photoresist layer 1208 is stripped away 1212 leaving exposed nanowires 100, ready for compression against an opposing conductive pad and for direct metal bonding with the opposing conductive pad. The polymer layer 1204 may be partly removed 1214, depending on implementation.



FIG. 13 shows another example process of creating nanowires 100 through a combination lithography process. In this process, the nanoporous layer is completely removed, with nanowires 100 grown directly on pads or traces to be bonded.


A chip, die, or wafer 1300 has conductive traces 1302, onto which a film of polymer 1304 or other material is spread for becoming a nanoporous layer for creating the nanowires 100. The polymer layer 1304 may be baked, if needed.


A photoresist layer 1306 is deposited over the polymer layer 1304. Photolithography of the photoresist layer 1306 makes nanopores 1308 in the photoresist layer 1306. Alternatively, the photoresist layer 1306 is just a resist that is etched in another manner to make the nanopores 1308, without light. The nanopores may be 200 nm in diameter, or smaller.


The nanopores 1308 in the photoresist layer 1306 are used to etch through the polymer layer 1304, to make extended nanopores 1310 down to the conductive pad 1302 of the chip, die, or wafer 1300.


Copper metal, or another metal, is plated or otherwise grown on the conductive pads 1302, forming the nanowires 100.


The photoresist layer 1306 is stripped away 1312 leaving exposed nanowires 100, ready for compression against an opposing conductive pad and for direct metal bonding with the opposing conductive pad. The nanoporous polymer layer 1304 is then removed 1314, leaving only conductive pads 1302 and the nanowires 100.



FIG. 14 shows an example nanowire bonding interface 102 in which the nanowires 100 are surmounted or mixed with a flowable joining material, such as tin metal (Sn) 1402 or a combination solder alloy. The “tinned” nanowires 100 may bond by elevating a temperature to the melting point of the tin or solder, or by compressive pressure when the solder or alloy is malleable, or by both raised temperature and applied pressure.


In an implementation, the nanowires 100 may be coated with the flowable joining material, such as a solder, and then heat and/or pressure may be applied to cause the solder or other flowable joining material on the nanowires 100 or opposing conductive pad to flow, making a solder bond.


In an implementation, the nanowire bonding interface 102 also includes a layer or film of a second metal besides tin, such as a nickel (Ni) layer 1404. A given microelectronics package 104 may use one of many different intermetallic compounds formed during solidifying of solders and during their reactions with the surfaces being soldered. The intermetallics may form distinct phases as inclusions in a ductile solid solution matrix or can form the matrix itself with metal inclusions, or can form various crystalline structures with different intermetallics. When the nanowires 100 are made of copper metal, a range of intermetallics may form between the copper metal and the tin or solder, with increasing proportion of the copper metal, such as Cu—Cu3Sn—Cu6Sn5—Sn, and so forth. Gold or palladium may be used as a coating to facilitate bonding because they readily dissolve in solders. Copper and nickel 1404 tend to form intermetallic layers during soldering processes, forming Ni3Sn4, for example, in the solder-nickel intermetallic interface.


In a variation, the example nanowires 100 are formed on the conductive pads 108 of one surface 1406 to be bonded, while the tin 1402 or solder alloy, and/or nickel 1404 are coated or formed on opposing conductive pads 108′ that have no nanowires 100, on the opposing surface 1408.



FIG. 15 shows an implementation of the nanowire bonding interface 1500, used in this scenario to make a flat top surface 1500 on a die, wafer, or device that has an uneven top surface 1502. The flat nanowire bonding interface 1500 may used for direct bonding, or other bonding, or may be used to create a spacer or interposer between dies, for example. The uneven surface 1502 of the die, wafer, or device is covered with a material 1504, which is then optionally flattened 1506. Pores are created in the material 1504, to make a nanoporous layer 1508. Nanowires 100 are then grown in the pores. Instead of the nanoporous layer 1508 being at least partially removed or recessed as in previously described implementations, the top surface 1500 of the nanoporous layer 1508 is flattened 1510, lapped, or polished by CMP or other planarizing techniques for direct bonding, or other bonding. The flat surface 1500 has planar cross-sectional ends of the nanowires 100 that have been grown in the pores of the nanoporous material 1508 and subsequently planarized 1510, and has remaining areas that consist of the flattened nanoporous material 1504. At this point, the flat surface 1500 can be direct-bonded through DBI® or other direct bonding techniques to conductive pads of an opposing surface 1514.



FIG. 16 shows another implementation of the nanowire bonding interface 102 in which the flat surface 1500 of FIG. 15 is used as a base to further grow the nanowires 100 to a greater vertical height 1602 by electroless plating of the same or a different metal, such as copper, nickel, gold, etc., or by metallic crystal growth, vapor deposition crystal growth, and so forth, on top of the existing nanowires 100.



FIG. 17 shows an example interposer 1700, with nanowires 100 disposed through the substrate 1702, in one implementation. The substrate 1702 may be porous silicon or oxidized alumina, ceramic, or other materials. The example interposer 1700 has a first side and a second side, wherein the nanowires 100 penetrate through the interposer 1700 to make respective layers of nanowire ends 1704 & 1706 on opposing sides of the interposer 1700. One or both sides of the nanowire ends 1704 & 1706 may be tinned or primed with solder or tin metal 1708 and/or another metal 1710, such as nickel, or alloy. The example two-sided interposer 1700 can bond a chip or wafer, or both chips and wafers, on both of its sides 1704 & 1706. The interposer 1700, including the respective layers of nanowire ends 1704 & 1706, may have a total thickness of approximately 100 μm or less.


Example Method


FIG. 18 shows an example method 1800 of creating a nanowire bonding interface. In the flow diagram of FIG. 18, operations of the example method 1800 are shown in individual blocks.


At block 1802, a material is deposited on at least a conductive pad of a bonding surface.


At block 1804, pores are created in the material deposited on the conductive pad to create a nanoporous layer.


At block 1806, nanowires of a metal are grown in the pores of the nanoporous layer.


At block 1808, at least a partial thickness of the nanoporous layer is removed or recessed to expose the nanowires for bonding with an opposing conductive pad.


In the foregoing description and in the accompanying drawings, specific terminology and drawing symbols have been set forth to provide a thorough understanding of the disclosed embodiments. In some instances, the terminology and symbols may imply specific details that are not required to practice those embodiments. For example, any of the specific dimensions, quantities, material types, fabrication steps and the like can be different from those described above in alternative embodiments. The term “coupled” is used herein to express a direct connection as well as a connection through one or more intervening circuits or structures. The terms “example,” “embodiment,” and “implementation” are used to express an example, not a preference or requirement. Also, the terms “may” and “can” are used interchangeably to denote optional (permissible) subject matter. The absence of either term should not be construed as meaning that a given feature or technique is required.


Various modifications and changes can be made to the embodiments presented herein without departing from the broader spirit and scope of the disclosure. For example, features or aspects of any of the embodiments can be applied in combination with any other of the embodiments or in place of counterpart features or aspects thereof. Accordingly, the specification and drawings are to be regarded in an illustrative rather than a restrictive sense.


While the present disclosure has been disclosed with respect to a limited number of embodiments, those skilled in the art, having the benefit of this disclosure, will appreciate numerous modifications and variations there from. It is intended that the appended claims cover such modifications and variations as fall within the true spirit and scope of the disclosure.

Claims
  • 1. A method, comprising: creating a nanoporous layer on a conductive pad of a microelectronic device or wafer;creating nanowires within pores of the nanoporous layer;removing or recessing at least part of the nanoporous layer to reveal at least a part of the nanowires for at least conductive contact with an opposing conductive surface of an opposing microelectronic device or wafer; anddirect hybrid bonding a bonding surface of the microelectronic device or wafer to the opposing microelectronic device or wafer, wherein the direct hybrid bonding comprises direct metal bonding the nanowires to the opposing conductive surface and direct bonding the nanoporous layer to the opposing microelectronic device or wafer.
  • 2. The method of claim 1, further comprising creating nanowires with a diameter less than 200 nanometers, wherein each nanowire has a height between approximately 200 nanometers and approximately 1000 nanometers (1 μm).
  • 3. The method of claim 1, wherein a height-to-diameter aspect ratio of each nanowire enables the nanowire to partially collapse against the opposing conductive surface providing a compression or a contact pressure of the nanowire for conductively contacting or bonding to the opposing conductive surface.
  • 4. The method of claim 1, wherein creating the nanoporous layer further comprises depositing a thin layer of a material on the conductive pad; and forming pores in the thin layer of the material via an etching process or a lithography process to make the nanoporous layer.
  • 5. The method of claim 1, further comprising flowing a joining material or a solder between the nanowires to conductively secure the nanowires to the opposing conductive surface.
  • 6. The method of claim 5, further comprising applying pressure to penetrate the nanowires through the solder.
  • 7. The method of claim 1, further comprising permanently joining the microelectronic device or wafer comprising the nanowires with a second microelectronic device or wafer comprising the opposing conductive surface with an adhesive.
  • 8. The method of claim 1, further comprising embedding metal pads laterally adjacent to between the conductive pad, the metal pads configured to vertically bond between surfaces being joined.
  • 9. The method of claim 8, wherein the metal pads comprise a heatsink.
  • 10. The method of claim 1 further comprising exposing a conductive surface of a through substrate via for forming nanowires thereupon.
  • 11. The method of claim 1, wherein each conductive pad comprises a length or a diameter less than approximately 5 μm.
  • 12. The method of claim 1, wherein multiple nanowires are conductively connected to each conductive pad.
  • 13. The method of claim 1, further comprising creating the nanoporous layer on at least the conductive pad and a portion of the bonding surface.
  • 14. The method of claim 13, further comprising creating nanowires within pores of the nanoporous layer at least at the conductive pad and the portion of the bonding surface.
  • 15. A method, comprising: forming a dielectric layer on at least a conductive pad and a portion of a bonding surface of a microelectronic device or wafer;forming nanowires within pores of the dielectric layer over the conductive pad;removing or recessing at least part of the dielectric layer to reveal at least a part of the nanowires for at least conductive contact with an opposing conductive surface of an opposing microelectronic device or wafer; anddirect hybrid bonding a bonding surface of the microelectronic device or wafer to the opposing microelectronic device or wafer, wherein the direct hybrid bonding comprises direct metal bonding the nanowires to the opposing conductive surface and directly bonding the dielectric layer on the portion of the bonding surface to the opposing microelectronic device or wafer.
  • 16. The method of claim 15, further comprising forming nanowires within pores of the dielectric layer at least at the conductive pad and the portion of the bonding surface.
  • 17. The method of claim 15, wherein the dielectric layer comprises a nanoporous layer.
  • 18. The method of claim 15, wherein forming the dielectric layer further comprises depositing a thin layer of a material on the conductive pad; and forming pores in the thin layer of the material via an etching process or a lithography process to make the dielectric layer.
  • 19. The method of claim 15, further comprising flowing a joining material or a solder between the nanowires to conductively secure the nanowires to the opposing conductive surface.
  • 20. The method of claim 15, wherein multiple nanowires are conductively connected to each conductive pad.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 16/776,182, filed on Jan. 29, 2020, and issued as U.S. Pat. No. 11,387,202, which claims priority to U.S. Provisional Patent Application No. 62/812,778 to Haba et al., filed Mar. 1, 2019, the contents of each of which are incorporated by reference herein in their entirety and for all purposes.

US Referenced Citations (236)
Number Name Date Kind
5753536 Sugiyama et al. May 1998 A
5771555 Eda et al. Jun 1998 A
6080640 Gardner et al. Jun 2000 A
6340822 Brown et al. Jan 2002 B1
6423640 Lee et al. Jul 2002 B1
6465892 Suga Oct 2002 B1
6887769 Kellar et al. May 2005 B2
6908027 Tolchinsky et al. Jun 2005 B2
7045453 Canaperi et al. May 2006 B2
7105980 Abbott et al. Sep 2006 B2
7193423 Dalton et al. Mar 2007 B1
7750488 Patti et al. Jul 2010 B2
7803693 Trezza Sep 2010 B2
8183127 Patti et al. May 2012 B2
8349635 Gan et al. Jan 2013 B1
8377798 Peng et al. Feb 2013 B2
8399982 Wyland Mar 2013 B2
8441131 Ryan May 2013 B2
8476165 Trickett et al. Jul 2013 B2
8482132 Yang et al. Jul 2013 B2
8501537 Sadaka 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
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
9362143 Sun et al. Jun 2016 B2
9385024 Tong et al. Jul 2016 B2
9394161 Cheng et al. Jul 2016 B2
9431368 Enquist et al. Aug 2016 B2
9437572 Chen et al. Sep 2016 B2
9443796 Chou et al. Sep 2016 B2
9461007 Chun et al. Oct 2016 B2
9496239 Edelstein et al. Nov 2016 B1
9536848 England et al. Jan 2017 B2
9559081 Lai et al. Jan 2017 B1
9620481 Edelstein et al. Apr 2017 B2
9656852 Cheng et al. May 2017 B2
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
9852988 Enquist et al. Dec 2017 B2
9871014 Haba 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
10002844 Wang et al. Jun 2018 B1
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
10418277 Cheng et al. Sep 2019 B2
10446456 Shen et al. Oct 2019 B2
10446487 Huang et al. Oct 2019 B2
10446532 Uzoh et al. Oct 2019 B2
10508030 Katkar et al. Dec 2019 B2
10522499 Enquist et al. Dec 2019 B2
10707087 Uzoh et al. Jul 2020 B2
10784191 Huang et al. Sep 2020 B2
10790262 Uzoh et al. Sep 2020 B2
10840135 Uzoh Nov 2020 B2
10840205 Fountain, Jr. et al. Nov 2020 B2
10854578 Morein Dec 2020 B2
10879212 Uzoh et al. Dec 2020 B2
10886177 DeLaCruz et al. Jan 2021 B2
10892246 Uzoh Jan 2021 B2
10923408 Huang et al. Feb 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
11004757 Katkar et al. May 2021 B2
11011494 Gao et al. May 2021 B2
11011503 Wang et al. May 2021 B2
11031285 Katkar et al. Jun 2021 B2
11037919 Uzoh et al. Jun 2021 B2
11056348 Theil Jul 2021 B2
11069734 Katkar Jul 2021 B2
11088099 Katkar et al. Aug 2021 B2
11127738 DeLaCruz et al. Sep 2021 B2
11158573 Uzoh et al. Oct 2021 B2
11158606 Gao et al. Oct 2021 B2
11169326 Huang et al. Nov 2021 B2
11171117 Gao et al. Nov 2021 B2
11176450 Teig et al. Nov 2021 B2
11195748 Uzoh et al. Dec 2021 B2
11205625 DeLaCruz et al. Dec 2021 B2
11244920 Uzoh Feb 2022 B2
11256004 Haba et al. Feb 2022 B2
11264357 DeLaCruz et al. Mar 2022 B1
11276676 Enquist et al. Mar 2022 B2
11296044 Gao et al. Apr 2022 B2
11329034 Tao et al. May 2022 B2
11348898 DeLaCruz et al. May 2022 B2
11355404 Gao et al. Jun 2022 B2
11355443 Huang et al. Jun 2022 B2
11367652 Uzoh et al. Jun 2022 B2
11380597 Katkar et al. Jul 2022 B2
11385278 DeLaCruz et al. Jul 2022 B2
11387202 Haba et al. Jul 2022 B2
11387214 Wang et al. Jul 2022 B2
11476213 Haba et al. Oct 2022 B2
20040084414 Sakai et al. May 2004 A1
20060057945 Hsu et al. Mar 2006 A1
20070111386 Kim et al. May 2007 A1
20070148949 Suh Jun 2007 A1
20130092426 Wu Apr 2013 A1
20140105674 Hayashi et al. Apr 2014 A1
20140175655 Chen et al. Jun 2014 A1
20140217610 Jeng Aug 2014 A1
20150017763 Haba et al. Jan 2015 A1
20150064498 Tong Mar 2015 A1
20160250710 Starkovich et al. Sep 2016 A1
20160343682 Kawasaki Nov 2016 A1
20170179061 Arvin et al. Jun 2017 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
20180323177 Yu et al. Nov 2018 A1
20180323227 Zhang et al. Nov 2018 A1
20180331066 Uzoh et al. Nov 2018 A1
20190115277 Yu et al. Apr 2019 A1
20190131277 Yang et al. May 2019 A1
20190333550 Fisch Oct 2019 A1
20190385935 Gao et al. Dec 2019 A1
20190385966 Gao et al. Dec 2019 A1
20200013637 Haba Jan 2020 A1
20200013765 Fountain, Jr. et al. Jan 2020 A1
20200035641 Fountain, Jr. et al. Jan 2020 A1
20200075553 DeLaCruz et al. Mar 2020 A1
20200294908 Haba et al. Sep 2020 A1
20200328162 Haba et al. Oct 2020 A1
20200328164 DeLaCruz et al. Oct 2020 A1
20200395321 Katkar et al. Dec 2020 A1
20200411483 Uzoh et al. Dec 2020 A1
20210098412 Haba 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
20210193603 DeLaCruz et al. Jun 2021 A1
20210193624 DeLaCruz et al. Jun 2021 A1
20210193625 Katkar et al. Jun 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
20220077063 Haba Mar 2022 A1
20220077087 Haba Mar 2022 A1
20220139867 Uzoh May 2022 A1
20220139869 Gao et al. May 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
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
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
20240055407 Workman Feb 2024 A1
20240079376 Suwito et al. Mar 2024 A1
20240170411 Chang et al. May 2024 A1
20240186248 Haba et al. Jun 2024 A1
20240186268 Uzoh et al. Jun 2024 A1
20240186269 Haba Jun 2024 A1
20240203917 Katkar et al. Jun 2024 A1
20240213191 Theil et al. Jun 2024 A1
20240213210 Haba et al. Jun 2024 A1
20240217210 Zhao et al. Jul 2024 A1
20240222239 Gao et al. Jul 2024 A1
20240222315 Uzoh Jul 2024 A1
20240222319 Gao et al. Jul 2024 A1
Foreign Referenced Citations (5)
Number Date Country
2013-033786 Feb 2013 JP
2018-160519 Oct 2018 JP
20160036571 Apr 2016 KR
WO 2005043584 May 2005 WO
WO 2016010841 Jan 2016 WO
Non-Patent Literature Citations (12)
Entry
G. G. Zhang, and C. C. Wong, “Review of Direct Metal Bonding for Microelectronic Interconnections”, Advanced Materials for Micro—and Nano-Systems (AMMNS), DSpace@MIT, Date Published Jan. 2004, Downloaded on May 15, 2024. (Year: 2004).
Hiramatsu et al., “Aligned growth of single-walled and double-walled carbon nanotube films by control of catalyst preparation,” Ch. 10 of the Book: “Carbon Nanotubes—Synthesis, Characterization, Applications, ” edited by Siva Yellampalli, ISBN 978-953-307-497-9, Jul. 20, 2011, 26 pages.
International Search Report and Written Opinion dated Jun. 18, 2020, for International Application No. PCT/US2020/017715, 10 pages.
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.
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.
Plobi, A. et al., “Wafer direct bonding: tailoring adhesion between brittle materials,” Materials Science and Engineering Review Journal, 1999, R25, 88 pages.
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).
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, Electronics Weekly.com (“BUSH article”); however, the imaged part and the part shown in the BUSH article share the part number “ONSEMI AR0820.”.
SONY IMX260 image, a first cross section of Sony product labeled IMX260, showing a hybrid bonded back side illuminated CMOS image sensor with a pad opening for a wire bond. The second image shows a second cross-section with peripheral probe and wire bond pads in the bonded structure. The part in the images was shipped in Apr. 2016. Applicant makes no representation that the part in the images 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 image.”
Related Publications (1)
Number Date Country
20230105341 A1 Apr 2023 US
Provisional Applications (1)
Number Date Country
62812778 Mar 2019 US
Divisions (1)
Number Date Country
Parent 16776182 Jan 2020 US
Child 17811713 US