PROCESS FOR APPLYING A TWO-DIMENSIONAL MATERIAL TO A TARGET SUBSTRATE POST-LAMINATION
20230007789 · 2023-01-05
Inventors
- Elad Mentovich (Tel Aviv, IL)
- Boaz Atias (Maale Adumim, IL)
- Doron Naveh (Petah-Tikva, IL)
- Adi Levi (Rosh HaAyin, IL)
Cpc classification
H05K3/00
ELECTRICITY
International classification
Abstract
Processes for creating a two-dimensional-target structure are disclosed. An example process to create a two-dimensional-target structure may include the process of providing two-dimensional material grown on an initial substrate to create a two-dimensional-substrate structure; applying the two-dimensional-substrate structure to a target substrate via an adhesion promoter to create a lamination stack; applying a lamination process to the lamination stack; and then removing the initial substrate from the lamination stack, post-lamination, to create the two-dimensional-target structure. The two-dimensional-target structure may then be used in such rigid or flexible electronic devices and/or non-standard devices as the target substrate may be rigid or flexible and/or translucent in contrast to the initial substrate first used to grow the two-dimensional material.
Claims
1. A method of applying a two-dimensional material to a target substrate comprising: providing a target substrate; applying an adhesion promoter to a surface of the target substrate; applying a two-dimensional-substrate structure to the surface of the target substrate via the adhesion promoter to form a lamination stack, wherein the two-dimensional-substrate structure comprises an initial substrate layer and a two-dimensional material on at least one of a top surface of the initial substrate layer or a bottom surface of the initial substrate layer; applying a heat and a pressure to the lamination stack; and removing the initial substrate layer from the lamination stack, after the heat and the pressure are applied, to form a two-dimensional-target structure.
2. The method of claim 1, further comprising applying a heat and a pressure to the two-dimensional-target structure.
3. The method of claim 1, wherein the two-dimensional material comprises hexagonal Boron Nitride (h-BN), graphene, black phosphorus, black arsen-phosphorus, mxene, two-dimensional perovskites, or any combination thereof.
4. The method of claim 1, wherein the adhesion promoter layer comprises epoxy resin, polyester, silicone, rubber, polysulfides, polypropylene, polyethylene, polyurethane, polydimethylsiloxane (PDMS), polyimide (PI), parylene, polyetherimide (PEI), polyamide (PA), polylactic acid (PLA), hydrocarbon-based film adhesive, Kapton, self-assembled monolayer (SAM), parylen, polyvinyl alcohol PVA, Polystyrene PS, Polycarbonate (PC), cellulose acetate (CA), ethylene vinyl acetate (EVA), or any combination thereof.
5. The method of claim 1, wherein the initial substrate layer comprises nickel (Ni), copper (Cu), platina (Pt), cobalt (Co), chromium (Cr), iridium (Ir), manganese (Mn), iron (Fe), tungsten (W), silver (Ag), ruthenium (Ru), rhodium (Rh), gold (Au), molybdenum (Mo), palladium (Pd), gallium (Ga), Indium (In), tin (Sn), silicon (Si), silicon dioxide (SiO2), mica, sapphire, polymeric liquid glass, glass substrate, AI2O3 metals, hafnium, or any combination thereof.
6. The method of claim 1, wherein the target substrate comprises at least a semiconductor or other solid wafer.
7. The method of claim 6, wherein the semiconductor wafer comprises silicon (Si), germanium (Ge), II-VI compound, III-V compound, glass, sapphire, quartz, or any combination thereof.
8. The method of claim 1, wherein the target substrate comprises a polymer.
9. The method of claim 8, wherein the polymer comprises polyethylene terephthalate (PET), polydimethylsiloxane (PDMS), polytetrafluoroethylene (PTFE), low density polyethylene (LDPE), nylon, ply(vinylpyrrolidone) (PVP), polystyrene (PS), poly(methyl methacrylate) (PMMA), poly(vinyl alcohol) (PVA), poly(vinyl chloride) (PVC), poly(vinylidene fluoride) (PVDF), polyalactic acid (PLA), polyimide (PI), polyetherimide (PEI), polyamide (PA), acrylonitrile butadiene styrene (ANBS), styrenic resins, kapton, silicon (Si), silicon dioxide (SiO2), thin-film metal-oxide, or any combination thereof.
10. A method of applying a two-dimensional material to a target substrate comprising: providing a two-dimensional-substrate structure, wherein the two-dimensional-substrate structure comprises an initial substrate layer and a two-dimensional material on at least one of a top surface of the initial substrate layer or a bottom surface of the initial substrate layer; applying an adhesion promoter to a surface of the two-dimensional-substrate structure; applying a target substrate to the surface of the two-dimensional-substrate structure via the adhesion promoter to form a lamination stack; applying a heat and a pressure to the lamination stack; and removing the initial substrate layer from the lamination stack, after the heat and the pressure are applied, to form a two-dimensional-target structure.
11. The method of claim 10, further comprising applying a heat and a pressure to the two-dimensional-target structure.
12. The method of claim 10, wherein the two-dimensional material comprises hexagonal Boron Nitride (h-BN), graphene black phosphorus, black arsen-phosphorus, mxene, two-dimensional perovskites, or any combination thereof.
13. The method of claim 10, wherein the adhesion promoter layer comprises epoxy resin, polyester, silicone, rubber, polysulfides, polypropylene, polyethylene, polyurethane, polydimethylsiloxane (PDMS), polyimide (PI), parylene, polyetherimide (PEI), polyamide (PA), polylactic acid (PLA), hydrocarbon-based film adhesive, Kapton, self-assembled monolayer (SAM), parylen, polyvinyl alcohol PVA, Polystyrene PS, Polycarbonate (PC), cellulose acetate (CA), ethylene vinyl acetate (EVA), or any combination thereof.
14. The method of claim 10, wherein the initial substrate layer comprises nickel (Ni), copper (Cu), platina (Pt), cobalt (Co), chromium (Cr), iridium (Ir), manganese (Mn), iron (Fe), tungsten (W), silver (Ag), ruthenium (Ru), rhodium (Rh), gold (Au), molybdenum (Mo), palladium (Pd), gallium (Ga), Indium (In), tin (Sn), silicon (Si), silicon dioxide (SiO2), mica, sapphire, polymeric liquid glass, glass substrate, AI2O3 metals, hafnium, or any combination thereof.
15. The method of claim 10, wherein the target substrate comprises at least a semiconductor wafer or other solid wafer.
16. The method of claim 15, wherein the semiconductor wafer comprises silicon (Si), germanium (Ge), II-VI compound, III-V compound, glass, sapphire, quartz, or any combination thereof.
17. The method of claim 10, wherein the target substrate comprises a polymer.
18. The method of claim 17, wherein the polymer comprises polyethylene terephthalate (PET), polydimethylsiloxane (PDMS), polytetrafluoroethylene (PTFE), low density polyethylene (LDPE), nylon, ply(vinylpyrrolidone) (PVP), polystyrene (PS), poly(methyl methacrylate) (PMMA), poly(vinyl alcohol) (PVA), poly(vinyl chloride) (PVC), poly(vinylidene fluoride) (PVDF), polyalactic acid (PLA), polyimide (PI), polyetherimide (PEI), polyamide (PA), acrylonitrile butadiene styrene (ANBS), styrenic resins, or any combination thereof.
19. A two-dimensional-target structure formed by the process comprising the steps of: providing a target substrate; applying an adhesion promoter to a surface of the target substrate; applying a two-dimensional-substrate structure to the surface of the target substrate via the adhesion promoter to form a lamination stack, wherein the two-dimensional-substrate structure comprises an initial substrate layer and a two-dimensional material on at least one of a top surface of the initial substrate layer or a bottom surface of the initial substrate layer; applying a heat and a pressure to the lamination stack; and removing the initial substrate layer from the lamination stack, after the heat and the pressure are applied, to form a two-dimensional-target structure.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0028] Having thus described the disclosure in general terms, reference will now be made to the accompanying drawings, which are not necessarily drawn to scale, and wherein:
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
DETAILED DESCRIPTION
[0035] Example embodiments will now be described more fully hereinafter with reference to the accompanying drawings, in which some, but not all, embodiments are shown. Indeed, the embodiments may take many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will satisfy applicable legal requirements. Like reference numerals refer to like elements throughout. The terms “exemplary” and “example” as may be used herein are not provided to convey any qualitative assessment, but instead merely to convey an illustration of an example. As used herein, terms such as “front,” “rear,” “top,” “inside,” “outside,” “inner,” “outer,” etc. are used for explanatory purposes in the examples provided below to describe the relative position of certain components or portions of components. Furthermore, as would be evident to one of ordinary skill in the art in light of the present disclosure, the terms “substantially” and “approximately” indicate that the referenced element or associated description is accurate to within applicable engineering tolerances. Thus, use of any such terms should not be taken to limit the spirit and scope of embodiments of the present invention.
[0036] According to embodiments of the present invention, an initial substrate may be used to grow a two-dimensional material comprising insulative and conductive properties, which may collectively be referred to as a two-dimensional-substrate structure. The two-dimensional-substrate structure may be applied to a target substrate comprising rigid or flexible properties via an adhesion promoter to form a lamination stack, heat and pressure may then be applied under a vacuum or controlled gas atmosphere (such as the CVD System incorporated by reference herein) to the lamination stack, and then the initial substrate may be removed from the lamination stack to form a two-dimensional-target structure. By using an initial substrate to grow the two-dimensional material rather than growing the two-dimensional material directly on the target substrate, according to embodiments of the methods and structures described herein, the two-dimensional material can be applied to target substrates having properties that are not able to support the growth process. For example, the target structure may have a lower rigidity properties and lower melting points than the initial substrate, such as may be the case when the target structure is a flexible electronic device. As such, embodiments of the present invention may allow a two-dimensional-target structure to be applied to rigid or flexible electronic devices including composite membranes; composite membranes for audio speakers and receivers; composite membrane actuators; touch screens; foldable screens; foldable touch screens; flexible, stretchable, or foldable electronic devices; flexible LEDs; flexible photovoltaics; silicon-integration of 2D devices where 2D devices are connected with circuits implemented in silicon; light sources on silicon or other wafers; photodetectors integrated with wafers; transparent electrodes on rigid or flexible glass; rigid or flexible transparent electromagnetic shielding, and other such devices known in the art, wherein the target substrate (including the two-dimensional material) may have higher conductivity over conventional two-dimensional-target structures.
[0037] A lamination stack, generally, may be understood to be the stack, or layers, of materials used in electronic devices (e.g., a lamination stack may be used to form a PCB). For example, such materials may include a conductive substrate (e.g., metal) used to grow a two-dimensional material such as graphene, hexagonal Boron Nitride (h-BN), or other such rigid or flexible and conductive materials. According to embodiments of the present invention, the lamination stack may further include the target substrate and an adhesion promoter that is used to affix the target substrate to the two-dimensional-substrate structure. The lamination stack may be heated and pressurized to secure a bond between the two-dimensional material and the target structure via the adhesion promoter. The process of heating and pressurizing may also be referred to as a lamination process. In some aspects of the present invention, heat may be applied to the base of the lamination stack (e.g., from below the lamination stack), applied to the top of the lamination stack (e.g., from a heat-source placed above the lamination stack), or applied to surround the lamination stack (e.g., similar to an oven chamber heating the lamination stack from multiple sides).
[0038] In some embodiments, the target substrate may also comprise such rigid or flexible and conductive properties as the two-dimensional material or higher rigid or flexible and conductive properties from the two-dimensional material. In recent technology, there is an increasing demand for rigid or flexible, conductive, and/or translucent materials to be used in such devices as described herein. Accordingly, there is an increased demand for efficient processes to create the materials used in these devices
[0039] With reference to
[0040] The method (e.g.,
[0041] In some embodiments, the two-dimensional material may be grown using such methods known in the art to grow the two-dimensional materials listed herein on the respective initial substrates. For example, to grow graphene on an initial substrate comprising metal, the methods of segregation of bulk-dissolved carbon on the initial substrate or the method of surface decomposition of carbon-containing molecules may be used to grow graphene on the initial substrates.
[0042] With respect to
[0043] In some embodiments, the adhesion promoter may be applied to the target substrate, and the two-dimensional-substrate structure may be applied to the target substrate via the adhesion promoter, as shown in steps 1B, 2B, 3B of
[0044] In some embodiments, the initial substrate may be removed by any number of processes depending on the materials involved (e.g., the materials used in the initial substrate and the two-dimensional material grown on the initial substrate), which is described in further detail below.
[0045] In some embodiments, the initial substrate may comprise nickel (Ni), copper (Cu), platina (Pt), cobalt (Co), chromium (Cr), iridium (Ir), manganese (Mn), iron (Fe), tungsten (W), silver (Ag), ruthenium (Ru), rhodium (Rh), palladium (Pd), gallium (Ga), indium (In), tin (Sn), or any combination thereof. In some embodiments, the initial substrate may comprise other metals known in the art which may withstand heat and/or pressure used throughout the process herein described. In some embodiments, the two-dimensional materials that may grow from the above list may comprise graphene, hexagonal Boron Nitride (h-BN), transition-metal oxide, transition-metal dichalcogenide or any other elemental/molecular analogue thereof.
[0046] In some embodiments, the initial substrate may comprise non-metallic compounds such as sapphire, fused quartz, mica, graphite, graphene, carbon, III-V compounds, II-VI compounds, silicon (Si), germanium (Ge), selenium (Se), tellurium (Te), or any combination thereof. In some embodiments, the two-dimensional materials may be grown on a substrate made from the group of compounds listed supra.
[0047] In some embodiments, the two-dimensional material grown on the initial substrate may comprise hexagonal Boron Nitride (h-BN), graphene, black phosphorus, black arsen-phosphorus, mxene, two-dimensional perovskites, or any combination thereof. In some embodiments, the two-dimensional material may comprise such combinations of materials as gallium oxide (Ga.sub.2O.sub.3), germanium sulfide (GaS), germanium selenide (GaSe), germanium telluride (GaTe), indium oxide (In.sub.2O.sub.3), indium sulfide (InS, In.sub.2S.sub.3), indium selenide (InSe, In.sub.2Se.sub.3), indium tellurium (InTe, In.sub.2Te.sub.3), antimony sulfide (Sb.sub.2S.sub.3), antimony selenide (Sb.sub.2Se.sub.3), antimony telluride (Sb.sub.2Te.sub.3), germanium oxide (GeO), germanium sulfide (GeS), germanium selenide (GeSe), germanium telluride (GeTe), stin oxide (SnO.sub.x), tin sulfur (SnS.sub.x), tin selenium (SnSe.sub.x), and/or tin tellurium (SnTe.sub.x).
[0048] In some embodiments, the two-dimensional material may comprise such combinations of materials as molybdenum disulfide (MoS.sub.2), molybdenum diselenide (MoSe.sub.2), molybdenum telluride (MoTe.sub.2), tungsten disulfide (WS.sub.2), tungsten diselenide (WSe.sub.2), tungsten telluride (WTe.sub.2), tin disulfide (SnS.sub.2), tin diselenide (SnSe.sub.2), tin telluride (SnTe.sub.2), hafnium disulfide (HfS.sub.2), hafnium diselenide (HfSe.sub.2), hafnium telluride (HfTe.sub.2), platinum disulfide (PtS.sub.2), platinum diselenide (PtSe.sub.2), platinum telluride (PtTe.sub.2), titanium disulfide (TiS.sub.2), titanium diselenide (TiSe.sub.2), titanium telluride (TiTe.sub.2), rhenium disulfide (ReS.sub.2), rhenium diselenide (ReSe.sub.2), or rhenium telluride (ReTe.sub.2).
[0049] In some embodiments, the two-dimensional material grown on the initial substrate listed supra, which may comprise such materials as bismuth (Bi), antimony (Sb), tin (Sn), oxygen (O), sulfur (S), selenium (Se), tellurium (Te), or any combination thereof. In some embodiments, the two-dimensional material may comprise such combinations of materials as bismuth(III) oxide (Bi.sub.2O.sub.3), bismuth sulfide (Bi.sub.2S.sub.3), bismuth(III) selenide (Bi.sub.2Se.sub.3), bismuth telluride (Bi.sub.2Te.sub.3), antimony(III) oxide (Sb.sub.2O.sub.3), antimony sulfide (Sb.sub.2S.sub.3), antimony triselenide (Sb.sub.2Se.sub.3), antimony telluride (Sb.sub.2Te.sub.3), tin(II) oxide (Sn.sub.2O.sub.3), tin(II) sulfide (Sn.sub.2S.sub.3), tin(II) sulfide (Sn.sub.2Se.sub.3), or tin(II) telluride (Sn.sub.2Te.sub.3).
[0050] In some embodiments, the adhesion promoter used in the present invention may comprise hydrocarbon-based thin film adhesive, epoxy resin, polyester, silicone, rubber, polysulfides, polypropylene, polyethylene, polyurethane, polydimethylsiloxane (PDMS), polyimide (PI), parylene, polyetherimide (PEI), polyamide (PA), polylactic acid (PLA), kapton, self-assembled monolayer (SAM), parylen, polyvinyl alcohol PVA, polystyrene PS, polycarbonate (PC), cellulose acetate (CA), ethylene vinyl acetate (EVA), hexagonal Boron-Nitride (h-BN), or any combination thereof.
[0051] In some embodiments, the target substrate may comprise polydimethylsiloxane polyethylene terephthalate (PET), polydimethylsiloxane (PDMS), polytetrafluoroethylene (PTFE), low density polyethylene (LDPE), nylon, poly(vinylpyrrolidone) (PVP), polystyrene (PS), poly(methyl methacrylate) (PMMA), poly(vinyl alcohol) (PVA), poly(vinyl chloride) (PVC), poly(vinylidene fluoride) (PVDF), polyalactic acid (PLA), polyimide (PI), polyetherimide (PEI), polyamide (PA), acrylonitrile butadiene styrene (ANBS), styrenic resins (e.g., ABS, ASA, SMA), kapton, silicon (Si), silicon dioxide (SiO2), thin-film metal-oxide, or any combination thereof.
[0052] In some embodiments, the target substrate may comprise at least a semiconductor wafer or other solid wafer. In some embodiments, the semiconductor wafer (e.g., target substrate) may further comprise silicon (Si), germanium (Ge), II-VI compound, III-V compound, glass, sapphire, quartz, or any combination thereof.
[0053]
[0054] The method (e.g., method 300) may include the step of providing a two-dimensional-substrate structure, wherein the two-dimensional-substrate comprises a substrate layer (i.e., initial substrate layer), at step 301. As described above with reference to
[0055] With reference to
[0056] The method (e.g., method 400) may include the step of providing a target substrate at step 401. At step 402, an adhesion promoter may be applied to a surface of the target substrate. The two-dimensional-substrate structure (previously grown) may be applied to the target substrate via the adhesion promoter to form the lamination stack at step 403, wherein the two-dimensional-substrate structure comprises an initial substrate layer. As described above with reference to
[0057] In some embodiments, the initial substrate—post-lamination—may be removed via a process of metal etching of the initial substrate with certain metal etchants. For example, if the initial substrate comprises copper (Cu), then a copper etchant may be used to remove the initial substrate from the two-dimensional material. Similarly, if using nickel as an initial substrate, then a nickel etchant may be used. It may be understood by one of skill in the art, that each of the initial substrates listed herein may comprise different metal etchants.
[0058] In some embodiments, the initial substrate may be removed—post-lamination—via a process of applying a sacrificial substrate layer, further comprising transition metal dichalcogenide (TMDC) on a silicon/silicon dioxide substrate (Si/SiO.sub.2). In some embodiments, the two-dimensional material may comprise the TMDC and the initial substrate may comprise Si/SiO.sub.2. In some embodiments, the Si/SiO.sub.2 may be etched using known methods in the art at the time of this application. A sacrificial layer (e.g., an initial substrate such as nickel) may be used to grow the graphene, then the sacrificial layer (e.g., nickel) with the two-dimensional material may be transferred and attached to a target substrate such that the two-dimensional material is between the target substrate and the initial layer. Once the two-dimensional material has been attached to the target substrate, the initial layer may be etched from to expose a surface of the two-dimensional material (e.g., the surface previously occupied by the initial substrate).
[0059] In some embodiments, the two-dimensional materials may be grown on oxide materials comprising sapphire, and SiO.sub.2. For those oxide materials, further including the two-dimensional material grown on the oxide materials, the process to remove the initial substrate (e.g., oxide material) may comprise an interfacial removal by water absorption between a hydrophobic and hydrophilic interface. Such hydrophobic materials may comprise those materials that are repellant to water which comprise a contact angle of greater than 90 degrees (e.g., graphene). In contrast, hydrophilic materials may comprise those materials that are repellant to water, which comprise a contact angel of lesser than 90 degrees (e.g., sapphire, SiO.sub.2). In such interfacial removal processes via water absorption, water in liquid state or gaseous state (e.g., bubbles) may be applied to the lamination structure to separate the initial substrate from the two-dimensional material.
[0060] Many modifications and other embodiments of the present inventions set forth herein will come to mind to one skilled in the art to which these inventions pertain having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the present inventions are not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims. Moreover, although the foregoing descriptions and the associated drawings describe example embodiments in the context of certain example combinations of elements and/or functions, it should be appreciated that different combinations of elements and/or functions may be provided by alternative embodiments without departing from the scope of the appended claims. In this regard, for example, different combinations of elements and/or functions than those explicitly described above are also contemplated as may be set forth in some of the appended claims. Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.