The field relates to microelectronics with functional and non-functional conductive (e.g., metal) pads in a bonding layer.
The semiconductor industry has experienced tremendous growth over the past several decades as engineers have developed chips with ever smaller transistors integrated thereon, as correctly predicted by Moore's Law. However, the industry is aware that the effort to reduce transistor size on silicon chips is approaching a physical limit. Meanwhile, consumer electronics, including computers and smart phones, continue to grow more and more complex, requiring effective utilization of a large numbers of transistors. One approach to improve three-dimensional (3D) integration is to stack chips or wafers on top of each other to form a 3D integrated structure. Direct hybrid bonding enables higher density interconnects between stacked elements. However, direct bonding between semiconductor elements utilizes planarized bonding surfaces with tight flatness tolerance which may create challenges.
Specific implementations will now be described with reference to the following drawings, which are provided by way of example, and not limitation.
When a bonding layer is formed over a semiconductor element, conductive contact pads are embedded in a nonconductive (e.g., dielectric) layer. A chemical mechanical processing (CMP) is performed to remove extra material on the dielectric layer to planarize the surface. The semiconductor can be prepared to be directly bonded to another semiconductor element or device without an intervening adhesive. Due to thermal expansion mismatch between the metal and the dielectric materials that are used, the thin film processes may result in stress in the bonding layer, e.g., the metal traces under tension and the dielectric material under compression. This stress can cause deformation and/or warpage in the semiconductor element, e.g., a device die or chip, a wafer, or a passive device. Therefore, there is a continuing need to reduce stresses in bonding layers and distortion in semiconductor elements.
To reduce the stress and distortion in the bonding layer due to the metal and dielectric material thermal expansion mismatch, in various embodiments, electrically non-functional (or dummy) metal pads can be embedded in the non-conductive dielectric material of the bonding layer to the regions that have no or fewer functional metal pads. This can be done in a way that the distribution of metal pads in dielectric material, including functional and non-functional, becomes more uniform. Thermal expansion mismatch between two mingled materials results in one material under tension and the other under compression. The thermal expansion coefficient of a metal, e.g., copper, is usually greater than the thermal expansion coefficient of a dielectric material, e.g., silicon oxide. Therefore, during a deposition or annealing process (or other process that uses elevated temperatures) when a semiconductor element cools down from an elevated temperature, the metal shrinks more than the dielectric material. Because the two materials are disposed side-by-side, the metal may be under tension and the dielectric material may be under compression. If the two materials are uniformly distributed with each other, however, the expansion of one material can be absorbed or counteracted by the contraction of the other. As such, the tensile and compressive stresses can be reduced or controlled. Therefore, uniform or approximately uniform distribution of metal pads in the dielectric material helps relieve the stress due to thermal expansion mismatch, and reduces distortion.
In various embodiments, the electrically non-functional or dummy metal pads in the interconnect or bonding layer may be shallower than the electrically functional or active pads. If the non-functional metal pads were to extend to a greater depth (e.g., to the same depth as the functional pads), then the dummy pads may short the metal traces buried in the interconnect layers below the dummy pad(s).
Conventionally, the functional metal pads in the dielectric layer may be formed by a dual damascene process.
A dual damascene process can be used to form the functional metal pads 112 together with the vias 110 in the dielectric layer 106 in
One characteristic of the dual damascene process shown in
Therefore, there is a motivation to replace the relatively complex dual damascene process using expensive masks with a simpler fabrication process. A single damascene process can reduce processing costs and simply fabrication.
The conductive (e.g., metal) layer 208 can be buried or embedded in the dielectric layer 204 close to the device layer 202. In some embodiments, the interconnect metal layer 208 can be an outermost layer of the device layer 202, e.g., the metal layer 208 may be formed in a dielectric layer provided over a semiconductor portion of the device layer 202 in a back-end-of-line (BEOL) process. In some embodiments, the metal layer 208 can be a redistribution layer (RDL) provided before the second dielectric layer 206 is deposited. The metal layer 208 can electrically communicate with one or more devices in the device layer 202 in some embodiments, e.g., maybe electrically connected to the active circuitry 201 in the device layer 202 through a via 205. At least one functional or active metal pad 212 and at least one non-functional metal pads 214 can be partially embedded in the second dielectric layer 206. Whereas the functional or active metal pads 212 extend from a top surface 216 through at least a portion of the second dielectric layer 206 to connect to (e.g., to contact) the buried metal layer 208, the non-functional metal pads 214 extends from the top surface 216 and terminates at a location shallower than the functional metal pads 212. The metal contact pads 212, 214 may take different cross-sectional shapes and dimensions, e.g., width or diameter, as viewed in the top surface 216, e.g., square, triangular, round, polygon, and etc. of different sizes. In some embodiments, the functional metal pads 212 can have a same first shape with a same first dimension, and the non-functional metal pads 214 can have a same second shape with a same second dimension. In some embodiments, the functional metal and the non-functional metal pads 212, 214 can have the same shape with the same dimension. In other embodiments, the functional metal pads 212 and the non-functional metal pads 214 may have different shapes and/or different dimensions. As can be seen in
Accordingly, in various embodiments disclosed herein, the functional conductive pads 212 can electrically connect to an electrically functional component of the semiconductor element 200, such as a trace (e.g., buried metal layer 208) that in turn connects to a device (e.g., circuitry 201) or any other suitable electrically functional component (e.g., interconnects in an interposer, a passive device, or any other suitable functional component). The dummy or nonfunctional pads 214 may be electrically inactive such that the dummy or electrically nonfunctional pads 214 are electrically isolated within the semiconductor element 200 (e.g., the dummy pads 214 do not electrically connect to a functional component or circuit in the semiconductor element 200). As explained herein in connection with
As compared to the structure of semiconductor element 100 in
Another example embodiment of the disclosure using a single damascene process to build functional and non-functional metal pads in a bonding layer is depicted in
As compared with
As shown in
In
Referring to
As explained herein, a plurality of (e.g., two) etching steps can be performed to form the functional and non-functional metal pads 312 and 314, respectively, in the semiconductor element 300 in
For example, one difference between the dual damascene process and the single damascene process are shown by the sidewall profiles of the holes or openings formed by the respective etch process(es), as discussed above with
The conductive feature 450 illustrated in
On the other hand, a conductive feature formed by the single damascene processes described herein does not have jagged or discontinuously angled sidewalls that are characteristic of conductive features formed by the dual damascene process as discussed above with
Returning to
After the metal filling process a planarization step, e.g., CMP, is applied to remove the excessive metal material to form a smooth top surface 316 of the second dielectric layer 306, as shown in
As shown in
As shown in
Referring now to
Various embodiments disclosed herein relate to directly bonded structures in which two or more elements can be directly bonded to one another without an intervening adhesive. Such processes and structures are referred to herein as “direct bonding” processes or “directly bonded” structures. Direct bonding can involve bonding of one material on one element and one material on the other element (also referred to as “uniform” direct bond herein), where the materials on the different elements need not be the same, without traditional adhesive materials. Direct bonding can also involve bonding of multiple materials on one element to multiple materials on the other element (e.g., hybrid bonding).
In some implementations (not illustrated), each bonding layer has one material. In these uniform direct bonding processes, only one material on each element is directly bonded. Example uniform direct bonding processes include the ZIBOND® techniques commercially available from Adeia of San Jose, CA. The materials of opposing bonding layers on the different elements can be the same or different, and may comprise elemental or compound materials. For example, in some embodiments, nonconductive bonding layers can be blanket deposited over the base substrate portions without being patterned with conductive features (e.g., without pads). In other embodiments, the bonding layers can be patterned on one or both elements, and can be the same or different from one another, but one material from each element is directly bonded without adhesive across surfaces of the elements (or across the surface of the smaller element if the elements are differently-sized). In another implementation of uniform direct bonding, one or both of the nonconductive bonding layers may include one or more conductive features, but the conductive features are not involved in the bonding. For example, in some implementations, opposing nonconductive bonding layers can be uniformly directly bonded to one another, and through substrate vias (TSVs) can be subsequently formed through one element after bonding to provide electrical communication to the other element.
In various embodiments, the bonding layers 808a and/or 808b can comprise a non-conductive material such as a dielectric material or an undoped semiconductor material, such as undoped silicon, which may include native oxide. Suitable dielectric bonding surface or materials for direct bonding include but are not limited to inorganic dielectrics, such as silicon oxide, silicon nitride, or silicon oxynitride, or can include carbon, such as silicon carbide, silicon oxycarbonitride, low K dielectric materials, SiCOH dielectrics, silicon carbonitride or diamond-like carbon or a material comprising a diamond surface. Such carbon-containing ceramic materials can be considered inorganic, despite the inclusion of carbon. In some embodiments, the dielectric materials at the bonding surface do not comprise polymer materials, such as epoxy (e.g., epoxy adhesives, cured epoxies, or epoxy composites such as FR-4 materials), resin or molding materials.
In other embodiments, the bonding layers can comprise an electrically conductive material, such as a deposited conductive oxide material, e.g., indium tin oxide (ITO), as disclosed in U.S. Provisional Patent Application No. 63/524,564, filed Jun. 30, 2023, the entire contents of which is incorporated by reference herein in its entirety for providing examples of conductive bonding layers without shorting contacts through the interface.
In direct bonding, first and second elements can be directly bonded to one another without an adhesive, which is different from a deposition process and results in a structurally different interface compared to that produced by deposition. In one application, a width of the first element in the bonded structure is similar to a width of the second element. In some other embodiments, a width of the first element in the bonded structure is different from a width of the second element. The width or area of the larger element in the bonded structure may be at least 10% larger than the width or area of the smaller element. Further, the interface between directly bonded structures, unlike the interface beneath deposited layers, can include a defect region in which nanometer-scale voids (nanovoids) are present. The nanovoids may be formed due to activation of one or both of the bonding surfaces (e.g., exposure to a plasma, explained below).
The bond interface between non-conductive bonding surfaces can include a higher concentration of materials from the activation and/or last chemical treatment processes compared to the bulk of the bonding layers. For example, in embodiments that utilize a nitrogen plasma for activation, a nitrogen concentration peak can be formed at the bond interface. In some embodiments, the nitrogen concentration peak may be detectable using secondary ion mass spectroscopy (SIMS) techniques. In various embodiments, for example, a nitrogen termination treatment (e.g., exposing the bonding surface to a nitrogen-containing plasma) can replace OH groups of a hydrolyzed (OH-terminated) surface with NH2 molecules, yielding a nitrogen-terminated surface. In embodiments that utilize an oxygen plasma for activation, an oxygen concentration peak can be formed at the bond interface between non-conductive bonding surfaces. In some embodiments, the bond interface can comprise silicon oxynitride, silicon oxycarbonitride, or silicon carbonitride. The direct bond can comprise a covalent bond, which is stronger than van Der Waals bonds. The bonding layers can also comprise polished surfaces that are planarized to a high degree of smoothness.
In direct bonding processes, such as uniform direct bonding and hybrid bonding, two elements are bonded together without an intervening adhesive. In non-direct bonding processes that utilize an adhesive, an intervening material is typically applied to one or both elements to effectuate a physical connection between the elements. For example, in some adhesive-based processes, a flowable adhesive (e.g., an organic adhesive, such as an epoxy), which can include conductive filler materials, can be applied to one or both elements and cured to form the physical (rather than chemical or covalent) connection between elements. Typical organic adhesives lack strong chemical or covalent bonds with either element. In such processes, the connections between the elements are weak and/or readily reversed, such as by reheating or defluxing.
By contrast, direct bonding processes join two elements by forming strong chemical bonds (e.g., covalent bonds) between opposing nonconductive materials. For example, in direct bonding processes between nonconductive materials, one or both nonconductive surfaces of the two elements are planarized and chemically prepared (e.g., activated and/or terminated) such that when the elements are brought into contact, strong chemical bonds (e.g., covalent bonds) are formed, which are stronger than Van der Waals or hydrogen bonds. In some implementations (e.g., between opposing dielectric surfaces, such as opposing silicon oxide surfaces), the chemical bonds can occur spontaneously at room temperature upon being brought into contact. In some implementations, the chemical bonds between opposing non-conductive materials can be strengthened after annealing the elements. As noted above, hybrid bonding is a species of direct bonding in which both non-conductive features directly bond to non-conductive features, and conductive features directly bond to conductive features of the elements being bonded. The non-conductive bonding materials and interface can be as described above, while the conductive bond can be formed, for example, as a direct metal-to-metal connection. In conventional metal bonding processes, a fusible metal alloy (e.g., solder) can be provided between the conductors of two elements, heated to melt the alloy, and cooled to form the connection between the two elements. The resulting bond often evinces sharp interfaces with conductors from both elements, and is subject to reversal by reheating. By way of contrast, direct metal bonding as employed in hybrid bonding does not require melting or an intermediate fusible metal alloy, and can result in strong mechanical and electrical connections, often demonstrating interdiffusion of the bonded conductive features with grain growth across the bonding interface between the elements, even without the much higher temperatures and pressures of thermocompression bonding.
The conductive features 806a and 806b of the illustrated embodiment are embedded in, and can be considered part of, a first bonding layer 808a of the first element 802 and a second bonding layer 808b of the second element 804, respectively. Field regions of the bonding layers 808a, 808b extend between and partially or fully surround the conductive features 806a, 806b. The bonding layers 808a, 808b can comprise layers of non-conductive materials suitable for direct bonding, as described above, and the field regions are directly bonded to one another without an adhesive. The non-conductive bonding layers 808a, 808b can be disposed on respective front sides 814a, 814b of base substrate portions 810a, 810b.
The first and second elements 802, 804 can comprise microelectronic elements, such as semiconductor elements, including, for example, integrated device dies, wafers, passive devices, discrete active devices such as power switches, MEMS, etc. In some embodiments, the base substrate portion can comprise a device portion, such as a bulk semiconductor (e.g., silicon) portion of the elements 802, 804, and back-end-of-line (BEOL) interconnect layers over such semiconductor portions. The bonding layers 808a, 808b can be provided as part of such BEOL layers during device fabrication, as part of redistribution layers (RDL), or as specific bonding layers added to existing devices, with bond pads extending from underlying contacts. Active devices and/or circuitry can be patterned and/or otherwise disposed in or on the base substrate portions 810a, 810b, and can electrically communicate with at least some of the conductive features 806a, 806b. Active devices and/or circuitry can be disposed at or near the front sides 814a, 814b of the base substrate portions 810a, 810b, and/or at or near opposite backsides 816a, 816b of the base substrate portions 810a, 810b. In other embodiments, the base substrate portions 810a, 810b may not include active circuitry, but may instead comprise dummy substrates, passive interposers, passive optical elements (e.g., glass substrates, gratings, lenses), etc. The bonding layers 808a, 808b are shown as being provided on the front sides of the elements, but similar bonding layers can be additionally or alternatively provided on the back sides of the elements.
In some embodiments, the base substrate portions 810a, 810b can have significantly different coefficients of thermal expansion (CTEs), and bonding elements that include such different based substrate portions can form a heterogenous bonded structure. The CTE difference between the base substrate portions 810a and 810b, and particularly between bulk semiconductor (typically single crystal) portions of the base substrate portions 810a, 810b, can be greater than 5 ppm/° C. or greater than 10 ppm/° C. For example, the CTE difference between the base substrate portions 810a and 810b can be in a range of 5 ppm/° C. to 100 ppm/° C., 5 ppm/° C. to 40 ppm/° C., 10 ppm/° C. to 100 ppm/° C., or 10 ppm/° C. to 40 ppm/° C.
In some embodiments, one of the base substrate portions 810a, 810b can comprise optoelectronic single crystal materials, including perovskite materials, that are useful for optical piezoelectric or pyroelectric applications, and the other of the base substrate portions 810a, 810b comprises a more conventional substrate material. For example, one of the base substrate portions 810a, 810b comprises lithium tantalate (LiTaO3) or lithium niobate (LiNbO3), and the other one of the base substrate portions 810a, 810b comprises silicon (Si), quartz, fused silica glass, sapphire, or a glass. In other embodiments, one of the base substrate portions 810a, 810b comprises a III-V single semiconductor material, such as gallium arsenide (GaAs) or gallium nitride (GaN), and the other one of the base substrate portions 810a, 810b can comprise a non-III-V semiconductor material, such as silicon (Si), or can comprise other materials with similar CTE, such as quartz, fused silica glass, sapphire, or a glass. In still other embodiments, one of the base substrate portions 810a, 810b comprises a semiconductor material and the other of the base substrate portions 810a, 810b comprises a packaging material, such as a glass, organic or ceramic substrate.
In some arrangements, the first element 802 can comprise a singulated element, such as a singulated integrated device die. In other arrangements, the first element 802 can comprise a carrier or substrate (e.g., a semiconductor wafer) that includes a plurality (e.g., tens, hundreds, or more) of device regions that, when singulated, forms a plurality of integrated device dies, though in other embodiments such a carrier can be a package substrate or a passive or active interposer. Similarly, the second element 804 can comprise a singulated element, such as a singulated integrated device die. In other arrangements, the second element 804 can comprise a carrier or substrate (e.g., a semiconductor wafer). The embodiments disclosed herein can accordingly apply to wafer-to-wafer (W2W), die-to-die (D2D), or die-to-wafer (D2W) bonding processes. In W2W processes, two or more wafers can be directly bonded to one another (e.g., direct hybrid bonded) and singulated using a suitable singulation process. After singulation, side edges of the singulated structure (e.g., the side edges of the two bonded elements) can be substantially flush (substantially aligned x-y dimensions) and/or the edges of the bonding interfaces for both bonded and singulated elements can be coextensive, and may include markings indicative of the common singulation process for the bonded structure (e.g., saw markings if a saw singulation process is used).
While only two elements 802, 804 are shown, any suitable number of elements can be stacked in the bonded structure 800. For example, a third element (not shown) can be stacked on the second element 804, a fourth element (not shown) can be stacked on the third element, and so forth. In such implementations, through substrate vias (TSVs) can be formed to provide vertical electrical communication between and/or among the vertically-stacked elements. Additionally or alternatively, one or more additional elements (not shown) can be stacked laterally adjacent one another along the first element 802. In some embodiments, a laterally stacked additional element may be smaller than the second element. In some embodiments, the bonded structure can be encapsulated with an insulating material, such as an inorganic dielectric (e.g., silicon oxide, silicon nitride, silicon oxynitrocarbide, etc.). One or more insulating layers can be provided over the bonded structure. For example, in some implementations, a first insulating layer can be conformally deposited over the bonded structure, and a second insulating layer (which may include be the same material as the first insulating layer, or a different material) can be provided over the first insulating layer.
To effectuate direct bonding between the bonding layers 808a, 808b, the bonding layers 808a, 808b can be prepared for direct bonding. Non-conductive bonding surfaces 812a, 812b at the upper or exterior surfaces of the bonding layers 808a, 808b can be prepared for direct bonding by polishing, for example, by chemical mechanical polishing (CMP). The roughness of the polished bonding surfaces 812a, 812b can be less than 30 Å rms. For example, the roughness of the bonding surfaces 812a and 812b can be in a range of about 0.1 Å rms to 15 Å rms, 0.5 Å rms to 10 Å rms, or 1 Å rms to 5 Å rms. Polishing can also be tuned to leave the conductive features 806a, 806b recessed relative to the field regions of the bonding layers 808a, 808b.
Preparation for direct bonding can also include cleaning and exposing one or both of the bonding surfaces 812a, 812b to a plasma and/or etchants to activate at least one of the surfaces 812a, 812b. In some embodiments, one or both of the surfaces 812a, 812b can be terminated with a species after activation or during activation (e.g., during the plasma and/or etch processes). Without being limited by theory, in some embodiments, the activation process can be performed to break chemical bonds at the bonding surface(s) 812a, 812b, and the termination process can provide additional chemical species at the bonding surface(s) 812a, 812b that alters the chemical bond and/or improves the bonding energy during direct bonding. In some embodiments, the activation and termination are provided in the same step, e.g., a plasma to activate and terminate the surface(s) 812a, 812b. In other embodiments, one or both of the bonding surfaces 812a, 812b can be terminated in a separate treatment to provide the additional species for direct bonding. In various embodiments, the terminating species can comprise nitrogen. For example, in some embodiments, the bonding surface(s) 812a, 812b can be exposed to a nitrogen-containing plasma. Other terminating species can be suitable for improving bonding energy, depending upon the materials of the bonding surfaces 812a, 812b. Further, in some embodiments, the bonding surface(s) 812a, 812b can be exposed to fluorine. For example, there may be one or multiple fluorine concentration peaks at or near a bond interface 818 between the first and second elements 802, 804. Typically, fluorine concentration peaks occur at interfaces between material layers. Additional examples of activation and/or termination treatments may be found in U.S. Pat. No. 9,391,143 at Col. 5, line 55 to Col. 7, line 3; Col. 8, line 52 to Col. 9, line 45; Col. 10, lines 24-36; Col. 11, lines 24-32, 42-47, 52-55, and 60-64; Col. 12, lines 3-14, 31-33, and 55-67; Col. 14, lines 38-40 and 44-50; and 10,434,749 at Col. 4, lines 41-50; Col. 5, lines 7-22, 39, 55-61; Col. 8, lines 25-31, 35-40, and 49-56; and Col. 12, lines 46-61, the activation and termination teachings of which are incorporated by reference herein.
Thus, in the directly bonded structure 800, the bond interface 818 between two non-conductive materials (e.g., the bonding layers 808a, 808b) can comprise a very smooth interface with higher nitrogen (or other terminating species) content and/or fluorine concentration peaks at the bond interface 818. In some embodiments, the nitrogen and/or fluorine concentration peaks may be detected using various types of inspection techniques, such as SIMS techniques. The polished bonding surfaces 812a and 812b can be slightly rougher (e.g., about 1 Å rms to 30 Å rms, 3 Å rms to 20 Å rms, or possibly rougher) after an activation process. In some embodiments, activation and/or termination can result in slightly smoother surfaces prior to bonding, such as where a plasma treatment preferentially erodes high points on the bonding surface.
The non-conductive bonding layers 808a and 808b can be directly bonded to one another without an adhesive. In some embodiments, the elements 802, 804 are brought together at room temperature, without the need for application of a voltage, and without the need for application of external pressure or force beyond that used to initiate contact between the two elements 802, 804. Contact alone can cause direct bonding between the non-conductive surfaces of the bonding layers 808a, 808b (e.g., covalent dielectric bonding). Subsequent annealing of the bonded structure 800 can cause the conductive features 806a, 806b to directly bond.
In some embodiments, prior to direct bonding, the conductive features 806a, 806b are recessed relative to the surrounding field regions, such that a total gap between opposing contacts after dielectric bonding and prior to anneal is less than 15 nm, or less than 10 nm. Because the recess depths for the conductive features 806a and 806b can vary across each element, due to process variation, the noted gap can represent a maximum or an average gap between corresponding conductive features 806a, 806b of two joined elements (prior to anneal). Upon annealing, the conductive features 806a and 806b can expand and contact one another to form a metal-to-metal direct bond.
During annealing, the conductive features 806a, 806b (e.g., metallic material) can expand while the direct bonds between surrounding non-conductive materials of the bonding layers 808a, 808b resist separation of the elements, such that the thermal expansion increases the internal contact pressure between the opposing conductive features. Annealing can also cause metallic grain growth across the bonding interface, such that grains from one element migrate across the bonding interface at least partially into the other element, and vice versa. Thus, in some hybrid bonding embodiments, opposing conductive materials are joined without heating above the conductive materials' melting temperature, such that bonds can form with lower anneal temperatures compared to soldering or thermocompression bonding.
In various embodiments, the conductive features 806a, 806b can comprise discrete pads, contacts, electrodes, or traces at least partially embedded in the non-conductive field regions of the bonding layers 808a, 808b. In some embodiments, the conductive features 806a, 806b can comprise exposed contact surfaces of TSVs (e.g., through silicon vias).
As noted above, in some embodiments, in the elements 802, 804 of
Beneficially, the use of hybrid bonding techniques (such as Direct Bond Interconnect, or DBI®, techniques commercially available from Adeia of San Jose, CA) can enable high density of connections between conductive features 806a, 806b across the direct bond interface 818 (e.g., small or fine pitches for regular arrays).
In some embodiments, a pitch p of the conductive features 806a, 806b, such as conductive traces embedded in the bonding surface of one of the bonded elements, may be less than 40 μm, less than 20 μm, less than 10 μm, less than 5 μm, less than 2 μm, or even less than 1 μm. For some applications, the ratio of the pitch of the conductive features 806a and 806b to one of the lateral dimensions (e.g., a diameter) of the bonding pad is less than is less than 20, or less than 10, or less than 5, or less than 3 and sometimes desirably less than 2. In various embodiments, the conductive features 806a and 806b and/or traces can comprise copper or copper alloys, although other metals may be suitable, such as nickel, aluminum, or alloys thereof. The conductive features disclosed herein, such as the conductive features 806a and 806b, can comprise fine-grain metal (e.g., a fine-grain copper). Further, a major lateral dimension (e.g., a pad diameter) can be small as well, e.g., in a range of about 0.25 μm to 30 μm, in a range of about 0.25 μm to 5 μm, or in a range of about 0.5 μm to 5 μm.
For hybrid bonded elements 802, 804, as shown, the orientations of one or more conductive features 806a, 806b from opposite elements can be opposite to one another. As is known in the art, conductive features in general can be formed with close to vertical sidewalls, particularly where directional reactive ion etching (RIE) defines the conductor sidewalls either directly though etching the conductive material or indirectly through etching surrounding insulators in damascene processes. However, some slight taper to the conductor sidewalls can be present, wherein the conductor becomes narrower farther away from the surface initially exposed to the etch. The taper can be even more pronounced when the conductive sidewall is defined directly or indirectly with isotropic wet or dry etching. In the illustrated embodiment, at least one conductive feature 806b in the bonding layer 808b (and/or at least one internal conductive feature, such as a BEOL feature) of the upper element 804 may be tapered or narrowed upwardly, away from the bonding surface 812b. By way of contrast, at least one conductive feature 806a in the bonding layer 808a (and/or at least one internal conductive feature, such as a BEOL feature) of the lower element 802 may be tapered or narrowed downwardly, away from the bonding surface 812a. Similarly, any bonding layers (not shown) on the backsides 816a, 816b of the elements 802, 804 may taper or narrow away from the backsides, with an opposite taper orientation relative to front side conductive features 806a, 806b of the same element.
As described above, in an anneal phase of hybrid bonding, the conductive features 806a, 806b can expand and contact one another to form a metal-to-metal direct bond. In some embodiments, the materials of the conductive features 806a, 806b of opposite elements 802, 804 can interdiffuse during the annealing process. In some embodiments, metal grains grow into each other across the bond interface 818. In some embodiments, the metal is or includes copper, which can have grains oriented along the 111 crystal plane for improved copper diffusion across the bond interface 818. In some embodiments, the conductive features 806a and 806b may include nanotwinned copper grain structure, which can aid in merging the conductive features during anneal. There is substantially no gap between the non-conductive bonding layers 808a and 808b at or near the bonded conductive features 806a and 806b. In some embodiments, a barrier layer may be provided under and/or laterally surrounding the conductive features 806a and 806b (e.g., which may include copper). In other embodiments, however, there may be no barrier layer under the conductive features 806a and 806b.
In various embodiments, the disclosure is a device comprising an interconnect structure having an upper surface prepared for direct bonding, a first contact pad extending to a first depth below the upper surface, and a second contact pad extending to a second depth below the upper surface, the second depth being less than the first depth.
In one aspect of the disclosure, the first contact pad comprises an active pad electrically connected to an underlying interconnect. Further, the first contact pad directly connects to the underlying interconnect without an intervening via.
In another aspect of the disclosure, the second contact pad comprises a dummy pad not electrically connected to the underlying interconnect.
In another aspect of the disclosure, the first contact pad and the second contact pad are made of metal. Further, the first contact pad and the second contact pad are made of copper.
In another aspect of the disclosure, the first contact pad is disposed in an opening having sidewalls that are continuous. Alternatively, the first contact pad is disposed in an opening having sidewalls that have no corner. The first contact pad is formed by a single damascene process.
In another aspect of the disclosure, the first pad and the second pad are approximately uniformly distributed on the upper surface of the interconnect structure. Alternatively, the first pad and the second pad are approximately uniformly distributed in the interconnect structure.
In another aspect of the disclosure, a ratio of the second depth to the first depth is greater than 50%. Alternatively, the ratio of the second depth to the first depth is greater than 85%.
In another aspect of the disclosure, the interconnect structure comprises a first dielectric layer comprises the upper surface, the first and second contact pads extending into the first dielectric layer.
In another aspect of the disclosure, the underlying interconnect is a redistribution layer (RDL) trace. Further, the underlying interconnect is an outermost metal layer of a microelectronic device.
In another aspect of the disclosure, the device further comprises a device layer, the device layer is disposed on the interconnect structure, wherein the device layer comprises circuitry electrically connected to the underlying interconnect.
In yet another aspect of the disclosure, the device layer comprises a complementary metal-oxide semiconductor (CMOS) device.
In some embodiments, the disclosure is a bonded structure comprising the device stated above and a second element comprising a second dielectric layer and a third contact pad at least partially embedded in the second dielectric layer, wherein the first dielectric layer is directly bonded to the second dielectric layer without an adhesive and the first contact pad is directly bonded to the third contact pad without an adhesive.
In some embodiments, the disclosure is a device comprising an interconnect structure having a surface prepared for direct bonding, and a plurality of pads embedded in the interconnect structure, the plurality of pads comprising a first plurality of active pads, and a second plurality of dummy pads, the dummy pads having a smaller thickness than the active pads.
In one aspect of the disclosure, each of the first plurality of active pads electrically connects to an underlying interconnect. Further, each of the first plurality of active pads directly connects to the underlying interconnect without an intervening via.
In another aspect of the disclosure, each of the second plurality of dummy pads is not electrically connected to the underlying interconnect.
In another aspect of the disclosure, the first plurality of active pads are formed by a single damascene process.
In another aspect of the disclosure, the plurality of pads are made of metal. Further, the plurality of pads are made of copper.
In another aspect of the disclosure, each active pad has sidewalls that are unitary. Alternatively, each active pad has sidewalls that have no corner.
In another aspect of the disclosure, the first plurality of active pads and the second plurality of dummy pads are approximately uniformly distributed on the surface of the interconnect structure. Alternatively, the first plurality of active pads and the second plurality of dummy pads are approximately uniformly distributed in the interconnect structure.
In another aspect of the disclosure, the surface of the interconnect structure comprises a first region having a first area density of the active pads and dummy pads with a first cross-sectional dimension and a second region having a second area density of the active pads and dummy pads with a second cross-sectional dimension, wherein the first area density is larger than the second area density, and wherein the second cross-sectional dimension is larger than the first cross-sectional dimension.
In yet another aspect of the disclosure, a ratio of the dummy pads thickness to the active pads thickness is greater than 50%. Further, the ratio of the depth is greater than 85%.
In some embodiments, the disclosure is a device comprising a device portion comprising a circuitry, an interconnect layer disposed on the device portion and having an upper bonding surface prepared for direct hybrid bonding to a second element, the interconnect layer comprising one or more non-conductive layers on the device portion, the one or more non-conductive layers having a first cavity and a second cavity formed therein, a buried conductive layer electrically connected to the circuitry and embedded in the one or more non-conductive layers at a first depth below the upper bonding surface, an electrically functional conductive pad disposed in the first cavity and extending from the upper bonding surface through at least a portion of the one or more non-conductive layers to connect to the buried conductive layer, the first cavity delimited by a continuous sidewall of the one or more non-conductive layers extending from the upper bonding surface, and an electrically non-functional conductive pad disposed in the second cavity and extending from the upper bonding surface through at least a portion of the one or more non-conductive layers, the electrically non-functional conductive pad terminating at a second depth that is less than the first depth.
In some embodiments, the disclosure is a method for fabricating a semiconductor element, comprising forming at least one first cavity in an interconnect layer of the semiconductor element, the at least one first cavity extending from an upper surface of the interconnect layer to a buried conductive layer of the semiconductor element, forming at least one second cavity in the interconnect layer laterally spaced apart from the at least one first cavity, the at least one second cavity extending from the upper surface of the interconnect layer and terminating at a depth of the dielectric layer above the buried conductive layer, providing a conductive material in the first and the second cavities, and preparing the upper surface of the interconnect layer for direct hybrid bonding to another element.
In one aspect of the disclosure, the method further comprising planarizing the upper surface by removing excessive metal material beyond the interconnect layer to form a bonding surface.
In another aspect of the disclosure, the conductive material is metal. Further, the conductive material is copper.
Unless the context clearly requires otherwise, throughout the description and the claims, the words “comprise,” “comprising,” “include,” “including” and the like are to be construed in an inclusive sense, as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including, but not limited to.” The word “coupled”, as generally used herein, refers to two or more elements that may be either directly connected, or connected by way of one or more intermediate elements. Likewise, the word “connected”, as generally used herein, refers to two or more elements that may be either directly connected, or connected by way of one or more intermediate elements. Additionally, the words “herein,” “above,” “below,” and words of similar import, when used in this application, shall refer to this application as a whole and not to any particular portions of this application. Moreover, as used herein, when a first element is described as being “on” or “over” a second element, the first element may be directly on or over the second element, such that the first and second elements directly contact, or the first element may be indirectly on or over the second element such that one or more elements intervene between the first and second elements. Where the context permits, words in the above Detailed Description using the singular or plural number may also include the plural or singular number respectively. The word “or” in reference to a list of two or more items, that word covers all of the following interpretations of the word: any of the items in the list, all of the items in the list, and any combination of the items in the list.
Moreover, conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” “for example,” “such as” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or states. Thus, such conditional language is not generally intended to imply that features, elements and/or states are in any way required for one or more embodiments.
While certain embodiments have been described, these embodiments have been presented by way of example only, and are not intended to limit the scope of the disclosure. Indeed, the novel apparatus, methods, and systems described herein may be embodied in a variety of other forms; furthermore, various omissions, substitutions, and changes in the form of the methods and systems described herein may be made without departing from the spirit of the disclosure. For example, while blocks are presented in a given arrangement, alternative embodiments may perform similar functionalities with different components and/or circuit topologies, and some blocks may be deleted, moved, added, subdivided, combined, and/or modified. Each of these blocks may be implemented in a variety of different ways. Any suitable combination of the elements and acts of the various embodiments described above can be combined to provide further embodiments. The accompanying claims and their equivalents are intended to cover such forms or modifications as would fall within the scope and spirit of the disclosure.
This application claims the benefit under 35 U.S.C. § 119(e)(1) of U.S. Provisional Application No. 63/477,551, filed Dec. 28, 2022, the entire content of which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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63477551 | Dec 2022 | US |