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Vladimir K Dioumaev

age ~58

from San Jose, CA

Also known as:
  • Valadimir K Dioumaev
  • Vladimir U

Vladimir Dioumaev Phones & Addresses

  • San Jose, CA
  • Mountain View, CA
  • Coram, NY
  • Philadelphia, PA
  • Upton, NY
  • 3615 Morrie Dr, San Jose, CA 95127

Work

  • Company:
    Capacitor sciences, inc.
    Apr 2018
  • Position:
    Senior scientist

Education

  • Degree:
    Doctorates, Doctor of Philosophy
  • School / High School:
    Mcgill University
    1992 to 1997
  • Specialities:
    Chemistry

Skills

Materials Science • Chemistry • Nanotechnology • Polymers • Semiconductors • Catalysis • Design of Experiments • Thin Films • Nanoparticles • Inorganic Chemistry • Spectroscopy • Coatings • Materials • Nanomaterials • Photovoltaics • Experimentation • Formulation • Electrochemistry • Process Simulation • Silicon • Mass Spectrometry

Languages

English • Russian

Industries

Research

Resumes

Vladimir Dioumaev Photo 1

Senior Scientist

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Location:
San Francisco, CA
Industry:
Research
Work:
Capacitor Sciences, Inc.
Senior Scientist

Nano Hydrophobics Dec 2016 - Apr 2018
Chief Technology Officer of Nano Hydrophobics

Enovix Corp. Aug 2009 - Sep 2016
Senior Principal Engineer, Engineering Manager 2, Enovix Corp

Nanogram Corporation Dec 2005 - Jun 2009
Senior Scientist

Kovio Mar 2004 - May 2005
Staff Scientist
Education:
Mcgill University 1992 - 1997
Doctorates, Doctor of Philosophy, Chemistry
Skills:
Materials Science
Chemistry
Nanotechnology
Polymers
Semiconductors
Catalysis
Design of Experiments
Thin Films
Nanoparticles
Inorganic Chemistry
Spectroscopy
Coatings
Materials
Nanomaterials
Photovoltaics
Experimentation
Formulation
Electrochemistry
Process Simulation
Silicon
Mass Spectrometry
Languages:
English
Russian

Us Patents

  • Recyclable Catalysts Methods Of Making And Using The Same

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  • US Patent:
    7005525, Feb 28, 2006
  • Filed:
    Dec 9, 2003
  • Appl. No.:
    10/731378
  • Inventors:
    Vladimir K. Dioumaev - Coram NY, US
    R. Morris Bullock - Wading River NY, US
  • Assignee:
    Brookhaven Science Associates, LLC - Upton NY
  • International Classification:
    C07F 11/00
    C07F 7/04
    C07C 29/04
    B01J 31/00
  • US Classification:
    548101, 556 59, 556470, 556482, 568809, 568814, 568881, 502152, 502155
  • Abstract:
    Organometallic complexes are provided, which include a catalyst containing a transition metal, a ligand and a component having the formula GAr. Aris an aromatic ring system selected from phenyl, naphthalenyl, anthracenyl, fluorenyl, or indenyl. The aromatic ring system has at least a substituent selected from fluorine, hydrogen, hydrocarbyl or fluorinated hydrocarbyl, G is substituted or unsubstituted (CH)or (CF), wherein n is from 1 to 30, wherein further one or more CHor CFgroups are optionally replaced by NR, PR, SiR, BR, O or S, or R is hydrocarbyl or substituted hydrocarbyl, GArbeing covalently bonded to either said transition metal or said ligand of said catalyst, thereby rendering said cationic organometallic complex liquid. The catalyst of the organometallic complex can be [CpM(CO)(NHC)L]A, wherein M is an atom of molybdenum or tungsten, Cp is substituted or unsubstituted cyclopentadienyl radical represented by the formula [CQQQQQ], wherein Qto Qare independently selected from the group consisting of H radical, GArChydrocarbyl radical, substituted hydrocarbyl radical, substituted hydrocarbyl radical substituted by GAr, halogen radical, halogen-substituted hydrocarbyl radical, —OR, —C(O)R′, —COR′, —SiR′and —NR′R″, wherein R′ and R″ are independently selected from the group consisting of H radical, Chydrocarbyl radical, halogen radical, and halogen-substituted hydrocarbyl radical, wherein said Qto Qradicals are optionally linked to each other to form a stable bridging group, NHC is any N-heterocyclic carbene ligand, L is either any neutral electron donor ligand, wherein k is a number from 0 to 1 or L is an anionic ligand wherein k is 2, and A is an anion. Processes using the organometallic complexes as catalysts in catalytic reactions, such as for example, the hydrosilylation of aldehydes, ketones and esters are also provided.
  • Methods Of Forming A Doped Semiconductor Thin Film, Doped Semiconductor Thin Film Structures, Doped Silane Compositions, And Methods Of Making Such Compositions

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  • US Patent:
    7314513, Jan 1, 2008
  • Filed:
    Sep 24, 2004
  • Appl. No.:
    10/949013
  • Inventors:
    Fabio Zürcher - Brisbane CA, US
    Wenzhuo Guo - Cupertino CA, US
    Joerg Rockenberger - Redwood City CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Brent Ridley - San Carlos CA, US
    Klaus Kunze - Albuquerque NM, US
    James Montague Cleeves - Redwood City CA, US
  • Assignee:
    Kovio, Inc. - Sunnyvale CA
  • International Classification:
    C09D 183/16
  • US Classification:
    10628714, 10618719, 2521823, 25218233, 25218235, 25218232
  • Abstract:
    Methods for forming doped silane and/or semiconductor thin films, doped liquid phase silane compositions useful in such methods, and doped semiconductor thin films and structures. The composition is generally liquid at ambient temperatures and includes a Group IVA atom source and a dopant source. By irradiating a doped liquid silane during at least part of its deposition, a thin, substantially uniform doped oligomerized/polymerized silane film may be formed on a substrate. Such irradiation is believed to convert the doped silane film into a relatively high-molecular weight species with relatively high viscosity and relatively low volatility, typically by cross-linking, isomerization, oligomerization and/or polymerization. A film formed by the irradiation of doped liquid silanes can later be converted (generally by heating and annealing/recrystallization) into a doped, hydrogenated, amorphous silicon film or a doped, at least partially polycrystalline silicon film suitable for electronic devices. Thus, the present invention enables use of high throughput, low cost equipment and techniques for making doped semiconductor films of commercial quality and quantity from doped “liquid silicon. ”.
  • Polysilane Compositions, Methods For Their Synthesis And Films Formed Therefrom

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  • US Patent:
    7485691, Feb 3, 2009
  • Filed:
    Oct 6, 2005
  • Appl. No.:
    11/246014
  • Inventors:
    Wenzhuo Guo - Cupertino CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Joerg Rockenberger - Redwood City CA, US
    Brent Ridley - San Carlos CA, US
  • Assignee:
    Kovio, Inc - Milpitas CA
  • International Classification:
    C08G 77/06
    C08G 77/12
    C08G 77/04
    C07F 7/04
    C07F 7/08
  • US Classification:
    528 17, 528 31, 528 33, 556430, 556487
  • Abstract:
    Polysilanes, inks containing the same, and methods for their preparation are disclosed. The polysilane generally has the formula H—[(AHR)(c-AH)]—H, where each instance of A is independently Si or Ge; R is H, —AHR, halogen, aryl or substituted aryl; (n+a)≧10 if q=0, q≧3 if n=0, and (n+q)≧6 if both n and q≠0; p is 1 or 2; and m is from 3 to 12. In one aspect, the method generally includes the steps of combining a silane compound of the formula AHR, the formula AHRand/or the formula c-AHRwith a catalyst of the formula RRMX(or an immobilized derivative thereof) to form a poly(aryl)silane; then washing the poly(aryl)silane with an aqueous washing composition and contacting the poly(aryl)silane with an adsorbent to remove the metal M. In another aspect, the method includes the steps of halogenating a polyarylsilane to form a halopolysilane; and reducing the halopolysilane with a metal hydride to form the polysilane. The synthesis of semiconductor inks via dehydrocoupling of silanes and/or germanes allows for tuning of the ink properties (e. g.
  • Polysilane Compositions, Methods For Their Synthesis And Films Formed Therefrom

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  • US Patent:
    7491782, Feb 17, 2009
  • Filed:
    Aug 13, 2007
  • Appl. No.:
    11/893054
  • Inventors:
    Wenzhuo Guo - Cupertino CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Joerg Rockenberger - Redwood City CA, US
    Brent Ridley - San Carlos CA, US
  • Assignee:
    Kovio, Inc. - Milpitas CA
  • International Classification:
    C08G 77/00
    C08G 77/04
    C08G 77/12
  • US Classification:
    528 10, 528 31, 528 33, 528 37, 528 43
  • Abstract:
    Polysilanes, inks containing the same, and methods for their preparation are disclosed. The polysilane generally has the formula H—[(AHR)(c-AH)]—H, where each instance of A is independently Si or Ge; R is H, —AHR, halogen, aryl or substituted aryl; (n+a)≧10 if q=0, q≧3 if n=0, and (n+q)≧6 if both n and q≠0; p is 1 or 2; and m is from 3 to 12. In one aspect, the method generally includes the steps of combining a silane compound of the formula AHR, the formula AHRand/or the formula c-AHRwith a catalyst of the formula RRMX(or an immobilized derivative thereof) to form a poly(aryl)silane; then washing the poly(aryl)silane with an aqueous washing composition and contacting the poly(aryl)silane with an adsorbent to remove the metal M. In another aspect, the method includes the steps of halogenating a polyarylsilane to form a halopolysilane; and reducing the halopolysilane with a metal hydride to form the polysilane. The synthesis of semiconductor inks via dehydrocoupling of silanes and/or germanes allows for tuning of the ink properties (e. g.
  • Dopant Group-Substituted Semiconductor Precursor Compounds, Compositions Containing The Same, And Methods Of Making Such Compounds And Compositions

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  • US Patent:
    7674926, Mar 9, 2010
  • Filed:
    Oct 1, 2004
  • Appl. No.:
    10/956714
  • Inventors:
    Wenzhuo Guo - Cupertino CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Brent Ridley - San Carlos CA, US
    Joerg Rockenberger - Redwood City CA, US
    James Montague Cleeves - Redwood City CA, US
  • Assignee:
    Kovio, Inc. - Milpitas CA
  • International Classification:
    C07F 5/02
    C07F 9/02
    C07F 9/30
    C07F 7/02
  • US Classification:
    556404, 556 7, 556 8, 556 19, 556 20, 556 30, 556402
  • Abstract:
    Dopant-group substituted (cyclo)silane compounds, liquid-phase compositions containing such compounds, and methods for making the same. Such compounds (and/or ink compositions containing the same) are useful for printing or spin coating a doped silane film onto a substrate that can easily be converted into a doped amorphous or polycrystalline silicon film suitable for electronic devices. Thus, the present invention advantageously provides commercial qualities and quantities of doped semiconductor films from a doped “liquid silicon” composition.
  • Polysilane Compositions, Methods For Their Synthesis And Films Formed Therefrom

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  • US Patent:
    7723457, May 25, 2010
  • Filed:
    Dec 31, 2008
  • Appl. No.:
    12/347911
  • Inventors:
    Wenzhuo Guo - Cupertino CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Joerg Rockenberger - Redwood City CA, US
    Brent Ridley - San Carlos CA, US
  • Assignee:
    Kovio, Inc. - Milpitas CA
  • International Classification:
    C08G 77/06
    C08G 77/12
    C08G 77/04
    C07F 7/04
    C07F 7/08
  • US Classification:
    528 31, 528 17, 528 33, 556430, 556487
  • Abstract:
    Polysilanes, inks containing the same, and methods for their preparation are disclosed. The polysilane generally has the formula H-[(AHR)(c-AH)]—H, where each instance of A is independently Si or Ge; R is H, -AHR, halogen, aryl or substituted aryl; (n+a)≧10 if q=0, q≧3 if n=0, and (n+q)≧6 if both n and q≠0; p is 1 or 2; and m is from 3 to 12. In one aspect, the method generally includes the steps of combining a silane compound of the formula AHR, the formula AHRand/or the formula c-AHRwith a catalyst of the formula RRMX(or an immobilized derivative thereof) to form a poly(aryl)silane; then washing the poly(aryl)silane with an aqueous washing composition and contacting the poly(aryl)silane with an adsorbent to remove the metal M. In another aspect, the method includes the steps of halogenating a polyarylsilane to form a halopolysilane; and reducing the halopolysilane with a metal hydride to form the polysilane. The synthesis of semiconductor inks via dehydrocoupling of silanes and/or germanes allows for tuning of the ink properties (e. g.
  • Linear And Cross-Linked High Molecular Weight Polysilanes, Polygermanes, And Copolymers Thereof, Compositions Containing The Same, And Methods Of Making And Using Such Compounds And Compositions

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  • US Patent:
    7943721, May 17, 2011
  • Filed:
    Oct 5, 2006
  • Appl. No.:
    11/543414
  • Inventors:
    Vladimir K. Dioumaev - Mountain View CA, US
  • Assignee:
    Kovio, Inc. - Milpitas CA
  • International Classification:
    C08G 77/08
  • US Classification:
    528 31, 528 15, 528 16, 528 17, 528 18, 528 34, 528 39
  • Abstract:
    Methods are disclosed of making linear and cross-linked, HMW (high molecular weight) polysilanes and polygermanes, polyperhydrosilanes and polyperhydrogermanes, functional liquids containing the same, and methods of using the liquids in a range of desirable applications. The silane and germane polymers are generally composed of chains of Si and/or Ge substituted with R′ substituents, where each instance of R′ is, for example, independently hydrogen, halogen, alkenyl, alkynyl, hydrocarbyl, aromatic hydrocarbyl, heterocyclic aromatic hydrocarbyl, SiR″, GeR″, PR″, OR″, NR″, or SR″; where each instance of R″ is independently hydrogen or hydrocarbyl. The cross-linked polymers can be synthesized by dehalogenative coupling or dehydrocoupling. The linear polymers can be synthesized by ring-opening polymerization. The polymers can be further modified by halogenation and/or reaction with the source of hydride to furnish perhydrosilane and perhydrogermane polymers, which are used in liquid ink formulations.
  • Doped Polysilanes, Compositions Containing The Same, Methods For Making The Same, And Films Formed Therefrom

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  • US Patent:
    7951892, May 31, 2011
  • Filed:
    Oct 11, 2005
  • Appl. No.:
    11/249167
  • Inventors:
    Wenzhuo Guo - Cupertino CA, US
    Vladimir K. Dioumaev - Mountain View CA, US
    Joerg Rockenberger - Redwood City CA, US
  • Assignee:
    Kovio, Inc. - Milpitas CA
  • International Classification:
    C08G 77/00
  • US Classification:
    528 17, 528 31, 528 43
  • Abstract:
    Doped polysilanes, inks containing the same, and methods for their preparation and use are disclosed. The doped polysilane generally has the formula H-[AH(DR)]-[(AHR)]—H, where each instance of A is independently Si or Ge, and D is B, P, As or Sb. In preferred embodiments, R is H, -AHR, alkyl, aryl or substituted aryl, and Ris independently H, halogen, aryl or substituted aryl. In one aspect, the method of making a doped poly(aryl)silane generally includes the steps of combining a doped silane of the formula AH(DR)(optionally further including a silane of the formula AHR) with a catalyst of the formula RRMX(or an immobilized derivative thereof) to form a doped poly(aryl)silane, then removing the metal M. In another aspect, the method of making a doped polysilane includes the steps of halogenating a doped polyarylsilane, and reducing the doped halopolysilane with a metal hydride to form the doped polysilane. The synthesis of semiconductor inks via dehydrocoupling of doped silanes and/or germanes allows for tuning of the ink properties (e. g.

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