Liquid silane-based compositions and methods for producing silicon-based materials

US9346966B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9346966-B2
Application numberUS-201213645551-A
CountryUS
Kind codeB2
Filing dateOct 5, 2012
Priority dateApr 6, 2010
Publication dateMay 24, 2016
Grant dateMay 24, 2016

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Abstract

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Described herein are synthesis schemes and methods for producing silicon based nanostructures and materials, including compositions and methods for synthesis of silicon-based nanowires and composites from three-component and four-component liquid silane/polymer inks. Materials and methods for producing silicon based micro and nanofibers that can be used in a variety of applications including material composites, electronic devices, sensors, photodetectors, batteries, ultracapacitors, and photosensitive substrates, and the like.

First claim

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What is claimed is: 1. A method for synthesizing silicon nanofibers, comprising: combining a liquid silane, a polymer and a solvent to form a viscous solution; passing a stream of viscous solution through a high electric field to form fibers; depositing the formed fibers onto a substrate; and transforming the deposited fibers. 2. A method as recited in claim 1 , wherein said liquid silane is a cyclosilane of the formula Si n H 2n selected from the group of cyclosilanes consisting of cyclopentasilane, cyclohexasilane and 1-silylcyclopentasilane. 3. A method as recited in claim 1 , wherein said liquid silane is a linear or branched cyclosilane of the formula Si n H 2n+2 . 4. A method as recited in claim 1 , wherein said polymer is selected from the group of polymers consisting of poly(methyl methacrylate), polycarbonate, poly(vinylidene fluoride-co-hexafluoropropylene), and polyvinyl butryal. 5. A method as recited in claim 1 , wherein said solvent is selected from the group of solvents consisting of toluene, xylene, cyclooctane, 1,2,4-trichlorobenzene, dichloromethane or mixtures thereof. 6. A method as recited in claim 1 , wherein said substrate is selected from the group of substrates consisting of a carbon fiber matte, a metal foil, and a mandrel. 7. A method as recited in claim 1 , wherein the deposited fibers are transformed using thermal processing at temperatures from 150° C. to 300° C. to produce polysilane-containing materials. 8. The method recited in claim 1 , wherein the deposited fibers are transformed using thermal processing at temperatures from 300° C. to 850° C. to produce amorphous silicon-containing materials. 9. The method as recited in claim 1 , wherein the deposited fibers are transformed using thermal processing at temperatures from 850° C. to 1414° C. to produce crystalline silicon-containing materials. 10. The method as recited in claim 1 , wherein the deposited fibers are transformed using laser processing to give crystalline silicon-containing materials. 11. A method for synthesizing silicon nanofibers, comprising: combining a liquid silane, a polymer, a solid phase and a solvent to form a viscous solution; passing a stream of viscous solution through a high electric field to form fibers; depositing the formed fibers onto a substrate; and transforming the deposited fibers. 12. A method as recited in claim 11 , wherein said liquid silane is a cyclosilane of the formula Si n H 2n selected from the group of cyclosilanes consisting of cyclopentasilane, cyclohexasilane and 1-silylcyclopentasilane. 13. A method as recited in claim 11 , wherein said liquid silane is a linear or branched cyclosilane of the formula Si n H 2n+2 . 14. A method as recited in claim 11 , wherein said solid phase is a metallic particle selected from the group of metal particles consisting of metallic particles of Al, Au, Ag, Cu, In—Sn—O, fluorine-doped tin oxide and carbon black. 15. A method as recited in claim 11 , wherein said solid phase is a semiconducting particle selected from the group of semiconducting particles consisting of carbon nanotubes, silicon nanowires, polydihydrosilane (Si n H 2 ) n , CdSe, CdTe, PbS, PbSe, ZnO and Si. 16. A method as recited in claim 11 , wherein said solid phase is a metal reagent selected from the group of metal reagents consisting of CaH 2 , CaBr 2 , Cp 2 Ti(CO) 2 , TiCl 4 , V(CO) 6 , Cr(CO) 6 , Cp 2 Cr, Mn 2 (CO) 10 , CpMn(CO) 3 , Fe(CO) 5 , Fe 2 (CO) 9 , Co 2 (CO) 8 , CO 4 (CO) 12 , Cp 2 Co, Cp 2 Ni, Ni(COD) 2 , BaH 2 , [Ru(CO) 4 ] ∞ , Os 3 (CO) 12 , Ru 3 (CO) 12 , HFeCo 3 (CO) 12 , and H 2 FeRu 3 (CO) 13 . 17. A method as recited in claim 11 , wherein said solid phase is a photoactive particle selected from the group of photoactive particles consisting of a carbon fullerene, a quantum dot of CdSe, PbS, Si or Ge, and a core-shell quantum dot of ZnSe/CdSe or Si/Ge. 18. A method as recited in claim 11 , further comprising: coating the transformed fibers with a coherent, conductive coating. 19. A method as recited in claim 11 , wherein the coating is a coating selected from the group of coatings consisting of graphite, carbon black, KB Carbon, carbon nanotubes and graphene. 20. A method of making silicon-containing composite wires comprising: combining a polymer and a solvent to form a viscous solution; flowing liquid silane through the inner annulus of a coaxial delivery tube while flowing the viscous polymer solution through the outer annulus; exposing the viscous mixture to a high electric field where continuous fibers are formed and deposited onto a substrate; and transforming the deposited fibers into a composite material that contains on the inside a polysilane, an amorphous silicon and/or a crystalline silicon fraction and on the outside a carbon coating. 21. A method as recited in claim 20 , wherein the liquid silane flowing through the inner annulus is selected from the group of cyclosilanes consisting of Si 6 H 12 cyclohexasilane, Si 6 H 12 1-silyl-cyclopentasilane and Si 5 H 10 cyclopentasilane. 22. A method as recited in claim 20 , wherein the liquid silane flowing through the inner annulus is selected from the group of linear and branched silanes having the formula Si n H 2n+2 . 23. A method as recited in claim 20 , wherein the solution flowing through the outer annulus is polyacrylonitrile in dimethylformamide. 24. A method for making silicon-containing battery electrode composite, comprising: combining a liquid silane of the formula Si n H 2n , with a polymer and a solvent to form a viscous solution; expelling the viscous solution through a high electric field wherein continuous fibers are formed and deposited onto a metal foil substrate; transforming the deposited fibers by thermal treatment under inert gas; forming a coherent, ion conductive coating on the transformed fibers; and mixing the coated silicon nanofibers with a binder and KB carbon to form an electrode.

Assignees

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Classifications

  • Nanowires · CPC title

  • Silicon, silicon germanium or germanium · CPC title

  • using solutions · CPC title

  • Cross-Sectional Technologies · mapped topic

  • C01B33/021Primary

    Preparation (chemical coating from the vapour phase C23C16/00) · CPC title

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What does patent US9346966B2 cover?
Described herein are synthesis schemes and methods for producing silicon based nanostructures and materials, including compositions and methods for synthesis of silicon-based nanowires and composites from three-component and four-component liquid silane/polymer inks. Materials and methods for producing silicon based micro and nanofibers that can be used in a variety of applications including ma…
Who is the assignee on this patent?
Ndsu Res Foundation
What technology area does this patent fall under?
Primary CPC classification C01B33/021. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 24 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).