WO2018165430A1 - Électrodes à hautes performances à domaines multiples, matériaux et précurseurs correspondants - Google Patents

Électrodes à hautes performances à domaines multiples, matériaux et précurseurs correspondants Download PDF

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Publication number
WO2018165430A1
WO2018165430A1 PCT/US2018/021551 US2018021551W WO2018165430A1 WO 2018165430 A1 WO2018165430 A1 WO 2018165430A1 US 2018021551 W US2018021551 W US 2018021551W WO 2018165430 A1 WO2018165430 A1 WO 2018165430A1
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Prior art keywords
thin film
carbon
micron
particles
conduit
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PCT/US2018/021551
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English (en)
Inventor
Ling FEI
Yong Lak Joo
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Axium Ip, Llc
Cornell University
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Publication of WO2018165430A1 publication Critical patent/WO2018165430A1/fr

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139—Processes of manufacture
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0402—Methods of deposition of the material
    • H01M4/0419—Methods of deposition of the material involving spraying
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0471—Processes of manufacture in general involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/386—Silicon or alloys based on silicon
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/483—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides for non-aqueous cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624—Electric conductive fillers
    • H01M4/625—Carbon or graphite
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B5/00—Electrostatic spraying apparatus; Spraying apparatus with means for charging the spray electrically; Apparatus for spraying liquids or other fluent materials by other electric means
    • B05B5/025—Discharge apparatus, e.g. electrostatic spray guns
    • B05B5/03—Discharge apparatus, e.g. electrostatic spray guns characterised by the use of gas, e.g. electrostatically assisted pneumatic spraying
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the field relates to electrodes, particularly negative electrodes in lithium ion batteries, cells and batteries comprising the same, and the manufacturing thereof.
  • Batteries comprise one or more electrochemical cell, such cells generally comprising a cathode, an anode and an electrolyte.
  • Lithium ion batteries are high energy density batteries that are fairly commonly used in consumer electronics and electric vehicles. In lithium ion batteries, lithium ions generally move from the negative electrode to the positive electrode during discharge and vice versa when charging. In the as-fabricated and discharged state, lithium ion batteries often comprise a lithium compound (such as a lithium metal oxide) at the cathode (positive electrode) and another material, generally carbon, at the anode (negative electrode).
  • Electrode materials and/or electrodes including thin layer electrodes, such as battery electrodes and/or electrode materials (e.g., lithium ion or lithium sulfur battery negative electrode materials and/or electrodes) (e.g., the thin layer electrode comprising a carbon and silicon).
  • battery electrodes and/or electrode materials e.g., lithium ion or lithium sulfur battery negative electrode materials and/or electrodes
  • the thin layer electrode comprising a carbon and silicon.
  • such materials and/or electrodes have excellent capacities, good capacity retention, high volumetric energy density (and high overall density), and/or other advantages that are discussed herein.
  • Alternate approaches to achieving higher performance materials and electrodes have had extremely limited and incremental success, with some attempts resulting in catastrophic failure, and/or development of un-scalable, cost prohibitive, and/or otherwise non- commercializable products and processes.
  • products and processes suitable for high throughput manufacturing and production including roll-to-roll processing, of high performance materials and electrodes, such as described in more detail herein.
  • an electrode material e.g., silicon-carbon electrode material
  • an electrode e.g., silicon-carbon electrode
  • the electrode material, electrode, or precursor thereof comprises an electrode active material (e.g., silicon, a silicon oxide, or a combination thereof), such as in the form of particles (e.g., nano- and/or micro-scale particles) comprising the same.
  • the composition or film materials e.g., thin film materials, such as thin film electrodes
  • the composition or film materials e.g., thin film materials, such as thin film electrodes
  • a first domain comprises a carbonaceous (e.g., grapheme) component and a (e.g., non-graphenic and non-graphitic) active electrode material, such as wherein the carbonaceous (e.g., grapheme) component forms a carbonaceous web securing the active electrode material therein.
  • a second domain comprises a second carbonacoues (e.g., grapheme) component, such as in the absence of the active electrode material (e.g., wherein the carbonaceous components of the first (base) and second (top) domains are the same or different).
  • the second domain is positioned in proximity to the separator and/or forms an interface with the electrolyte.
  • control of such morphologies facilitates better coverage and/or protection of the active electrode materials during lithiation and de-lithiation, such as by reducing delamination of the particles during usage (e.g., battery cycling).
  • such configuration functions to minimize or reduce unnecessary interaction between the active electrode material and the electrolyte, which may result in unwanted reactions and/or cycling inefficiencies.
  • the configuration functions to secure an increased fraction of the active electrode material to and/or within the film during cell cycling (e.g., even if the active electrode material fractures and/or breaks apart during cycling, it remains secure).
  • the second domain is thin enough to allow sufficient access to the active electrode material; otherwise, difficulty in allowing access (e.g., lithium ingress and egress) to the active electrode material causes inefficiencies of their own, such as illustrated herein.
  • a process for manufacturing a film comprises depositing a first (e.g., base) composition on a substrate (e.g., a current collector, such as a metal foil), followed by depositing a second (e.g., top) composition on the first composition, the film collectively comprising the first and second compositions.
  • a first (e.g., base) composition on a substrate (e.g., a current collector, such as a metal foil), followed by depositing a second (e.g., top) composition on the first composition, the film collectively comprising the first and second compositions.
  • the first composition comprises an active electrode material (e.g., a plurality of particles comprising SiOx) and a carbonaceous material (e.g., a conductive carbonacoues material, such as a grapheme component) and the second composition comprises a carbonaceous material (e.g., a conductive carbonacoues material, such as a graphenic component), wherein the carbonaceous material of the first and second compositions are the same or different.
  • active electrode material e.g., a plurality of particles comprising SiOx
  • a carbonaceous material e.g., a conductive carbonacoues material, such as a grapheme component
  • the second composition comprises a carbonaceous material (e.g., a conductive carbonacoues material, such as a graphenic component)
  • the first (e.g., base) composition is deposited by producing a first plume or aerosol from a first fluid stock (e.g., from a plume or aerosol producing nozzle, such as described herein), the first fluid stock comprising a plurality of first inclusion particles and a liquid medium, the first inclusion particles comprising a plurality of active electrode material-containing particles, and a plurality of first carbon inclusion components; and collecting the first composition on the substrate, the first composition comprising the plurality of first inclusion particles.
  • a first fluid stock e.g., from a plume or aerosol producing nozzle, such as described herein
  • the first fluid stock comprising a plurality of first inclusion particles and a liquid medium, the first inclusion particles comprising a plurality of active electrode material-containing particles, and a plurality of first carbon inclusion components
  • the process comprises depositing a plurality of second carbon inclusion components on the first composition, thereby forming a second (e.g., top) composition, the first and second carbon inclusion components being the same or different, and the first and second compositions collectively (or when taken together) forming a film (e.g., an electrode film or a precursor thereof).
  • depositing of the second carbon inclusion components on the first composition comprises producing a second plume or aerosol from a second fluid stock (e.g., from a plume or aerosol producing nozzle), the second fluid stock comprising a plurality of second inclusion particles and a liquid medium, the inclusion particles comprising the plurality of second carbon inclusions; and collecting the second composition on the first composition, the second composition comprising the plurality of second inclusion particles.
  • a second fluid stock e.g., from a plume or aerosol producing nozzle
  • the second fluid stock comprising a plurality of second inclusion particles and a liquid medium, the inclusion particles comprising the plurality of second carbon inclusions
  • the process further comprises thermally treating the first composition or the film.
  • a graphenic component with high oxygen content e.g., graphene oxide
  • thermal treatment of the first (e.g., base) composition and/or film functions to reduce the graphenic component (e.g., from graphene oxide to reduced graphene oxide).
  • the thermally treated film is utilized as an electrode provided herein with or without further processing.
  • Electrodes e.g., anodes
  • electrode materials provided herein can be used in any suitable battery, energy storage, or other electrode containing device.
  • the electrode provided herein is useful in a lithium battery, such as a lithium ion or lithium sulfur battery.
  • the battery comprises the electrode (e.g., as an anode), a separator, and a second electrode (e.g., a cathode), with the separator configured between the two electrodes.
  • the cathode of the lithium ion battery is a lithium metal oxide, lithium metal phosphate, or other suitable material.
  • the cathode of the lithium sulfur battery comprises a sulfur compound (e.g., a sulfide, polysulfide, organosulfur, sulfur, or the like), such as deposited on a carbon substrate (e.g., a porous carbon substrate).
  • a (e.g., first and/or second) plume or aerosol is generated by providing a (e.g., first and/or second) fluid stock to a first inlet of a first conduit of a nozzle, the first conduit being enclosed along the length of the conduit by a first wall having a first interior surface and a first exterior surface, the first conduit having a first outlet, and providing a voltage to the nozzle.
  • a first plume or aerosol is generated by providing a first fluid stock to a first inlet of a first conduit of a nozzle, the first conduit being enclosed along the length of the conduit by a first wall having a first interior surface and a first exterior surface, the first conduit having a first outlet, and providing a voltage to the first nozzle.
  • a second plume or aerosol is generated by providing the second fluid stock to a third inlet of a third conduit of a second nozzle, the third conduit being enclosed along the length of the third conduit by a third wall having a third interior surface and a third exterior surface, the third conduit having a third outlet, and providing a voltage to the second nozzle.
  • a plume or aerosol (e.g., the first and/or second plume or aerosol) is generated by electrospraying the fluid stock (e.g., with an electrospray nozzle).
  • the plume or aerosol (e.g., the first and/or second plume or aerosol) is generated in the presence of a high velocity gas (e.g., air), such as having a velocity of at least 0.1 m/s (e.g., at least 0.5 m/s, or more, such as described herein).
  • a high velocity gas is provided by providing a pressurized gas (e.g., air), such as to a nozzle producing the plume or aerosol.
  • a first plume or aerosol is generated by (i) providing a first fluid stock to a first inlet of a first conduit of a nozzle, the first conduit being enclosed along the length of the conduit by a first wall having a first interior surface and a first exterior surface, the first conduit having a first outlet, (ii) providing a voltage to the first nozzle, and (iii) providing a first pressurized gas to a second inlet of a second conduit of the first nozzle, the second conduit having a second inlet and a second outlet, and at least a portion of the second conduit being positioned in surrounding relation to the first conduit.
  • the second conduit is enclosed by a second wall, the second wall having a second interior surface.
  • the distance between the interior surface of the second wall and the exterior surface of the first wall is any suitable distance, such as about 0.01 mm to about 30 mm. In some embodiments, the distance between the interior surface of the second wall and the exterior surface of the first wall is suitable for providing a desired velocity at the nozzle outlet (e.g., at the first and/or second outlet), such as at least 0.5 m/s, or other suitable velocity described herein.
  • a second plume or aerosol is generated by providing a second fluid stock to a third inlet of a third conduit of a second nozzle, the third conduit being enclosed along the length of the third conduit by a third wall having a third interior surface and a third exterior surface, the third conduit having a third outlet, (ii) providing a voltage to the second nozzle, and (iii) providing a second pressurized gas to a fourth inlet of a fourth conduit of the second nozzle, the fourth conduit having a fourth inlet and a fourth outlet, and at least a portion of the fourth conduit being positioned in surrounding relation to the third conduit.
  • the fourth conduit is enclosed by a fourth wall, the fourth wall having an interior surface.
  • the distance between the interior surface of the fourth wall and the exterior surface of the third wall is any suitable distance, such as about 0.01 mm to about 30 mm. In some embodiments, the distance between the interior surface of the fourth wall and the exterior surface of the third wall is suitable for providing a desired velocity at the nozzle outlet (e.g., at the third and/or fourth outlet), such as at least 0.5 m/s, or other suitable velocity described herein.
  • films e.g., thin films
  • a first composition e.g., configured in a layered configuration, the first composition constituting a first domain and the second composition constituting a second domain
  • the first composition comprises about 50 wt. % or more (e.g., about 50 wt. % to about 99.9 wt. %) active electrode material (e.g., SiOx) or inclusions comprising active electrode material (e.g., SiOx).
  • the film or combination of the first and second compositions comprises at least 40 wt % (e.g., about 50 wt. % to about 95 wt. %) active electrode material (e.g., SiOx) or inclusions comprising active electrode material (e.g., SiOx).
  • active electrode material e.g., SiOx
  • inclusions comprising active electrode material e.g., SiOx
  • a thin film comprising a first domain and a second domain, the first domain comprising a plurality of particles (e.g., microparticles) secured within one or more carbonaceous web, the carbonaceous web comprising a plurality of first carbonaceous components, and the second domain comprising a plurality of second carbonaceous components, the first and second carbonaceous components being the same or different.
  • the plurality of particles and the plurality of first carbonaceous components are present in the first domain in a particle to first carbonaceous component weight ratio of about 1 : 10 to about 20: 1.
  • the first domain has a first average thickness
  • the second domain has a second average thickness
  • the ratio of the first average thickness to the second average thickness being at least 1 : 1.
  • the particles having an average smallest dimension of about 0.01 micron to about 10 micron.
  • the thin film having an average film thickness of about 50 micron or less.
  • the second domain is configured (e.g., forming a layer) on a surface of the first domain (e.g., which forms a layer on the substrate).
  • a substrate provided herein is a conductive substrate, such as a metal (e.g., metal foil), such as comprising aluminum or copper.
  • a first composition is collected on a substrate, such as wherein the substrate has a substrate surface in opposing relation to the first nozzle.
  • a second composition is collected on the first substrate, the first composition (e.g., a film) having a surface in opposing relation to the second nozzle.
  • a substrate is affixed to or a part of a conveyor system.
  • a substrate is provided in a roll, unrolled and conveyed in opposing relation to a first nozzle (or bank of first nozzles) (e.g., collecting a first composition on a surface thereof), subsequently conveyed in opposing relation to a second nozzle (or bank of second nozzles) (e.g., collecting a second composition on a surface of the first composition), and re-rolled (e.g., a roll- to-roll process).
  • the first composition or combination of the first and second composition is subjected to reductive conditions (e.g., thermos-reductive conditions suitable for reducing the oxygen content of a carbon inclusion (e.g., oxidized grapheme component) prior to or following re-rolling.
  • reductive conditions e.g., thermos-reductive conditions suitable for reducing the oxygen content of a carbon inclusion (e.g., oxidized grapheme component) prior to or following re-rolling.
  • any suitable active electrode material is optionally utilized, and is generally different from the carbon inclusion material.
  • the active electrode material is utilized in a process, composition, electrode or material herein in the form of an inclusion particle comprising the active electrode material.
  • the active electrode material is a silicon containing material, such as is active in lithium batteries.
  • the silicon-containing material has the formula SiOx, wherein 0 ⁇ x ⁇ 2.
  • 0 ⁇ x ⁇ 1.5 Preferably, 0 ⁇ x ⁇ 1.5. More preferably, 0 ⁇ x ⁇ 0.5.
  • the active electrode material-containing particles have an average smallest dimension of about 0.1 micron to about 50 micron (e.g., about 0.1 micron to about 15 micron, or about 0.5 to about 5 micron).
  • Some preferred active electrode material inclusion (e.g. particle) morphologies, including sizes, are further described in more detail herein and in co-pending U.S. Patent Application entitled “Active Materials for High Performance Electrodes, Materials, and Precursors Thereof," U.S. Provisional Application No. 62/468,867, which is incorporated by reference herein in its entirety.
  • carbon inclusion material (used interchangeably herein with “carbonaceous inclusion materials”) is optionally used in a process or composition herein.
  • exemplary carbon inclusion materials include carbon allotropes and analogs or derivatives thereof, such as those modified with hydrogen, oxygen, nitrogen, sulfur, halide, or the like, or combinations thereof.
  • the carbon allotropes can also include structural defects, such as opened or modified rings, or the like.
  • carbon inclusions include, by way of non- limiting example, carbon nanotubes, graphite, graphene, or analogs or derivatives thereof.
  • the carbon inclusion comprises graphene, graphene oxide, reduced graphene oxide, carbon nanotubes or a combination thereof.
  • reference to such materials includes those modified with other elements (e.g., less than 5 wt. %, less than 3 wt. %, less than 1 wt. %, or the like - for clarity, such amounts don't refer to the oxygen content of graphene oxide or reduced graphene oxide unless otherwise stated herein), such as hydrogen, oxygen, nitrogen, sulfur, halides, or the like, or combinations thereof and are pristine or comprise defects.
  • the carbon inclusion of the first and second fluid stocks or compositions are independently selected and are the same or different.
  • the carbon inclusion of the first and second fluid stocks and/or first and second compositions are independently selected from graphenic components, such as graphene oxides (e.g., optionally modified as discussed herein).
  • graphenic components such as graphene oxides (e.g., optionally modified as discussed herein).
  • the graphenic components comprise at least 50 wt. % carbon and about 10 wt. % to about 50 wt. % oxygen (e.g., and less than 5 wt. % other elements, such as described herein).
  • the first and second carbon inclusions are graphenic components (e.g., reduced graphene oxides) comprising at least 85 wt. % carbon and about 0.1 wt. % to about 15 wt. % oxygen (e.g., and less than 5 wt. % other elements, such as described herein). More details and/or alternative carbon inclusion (e.g., graphenic) components are described in more detail herein.
  • graphenic components e.g., reduced graphene oxides
  • graphenic components comprising at least 85 wt. % carbon and about 0.1 wt. % to about 15 wt. % oxygen (e.g., and less than 5 wt. % other elements, such as described herein). More details and/or alternative carbon inclusion (e.g., graphenic) components are described in more detail herein.
  • the carbonaceous components (e.g., of the first and/or second domain or composition) have an average lateral dimension that is equal to or greater than the average of the smallest dimension of the particles.
  • the average lateral dimension of the carbonaceous components is about ten times or less the average of the smallest dimension of the particles.
  • the second composition or fluid stock provided herein comprises less (e.g., non-graphitic/non-graphenic) active electrode material, active material inclusions, or SiOx than does the first composition.
  • the second composition or fluid stock comprises at least 25 % less (e.g., at least 50 % less, at least 75 % less, at least 85 % less, at least 90 % less, at least 95 % less, or the like) (e.g., by weight) (non-graphitic/non-graphenic) active electrode material, active material inclusions or SiOx than the first composition.
  • the first carbon inclusion constitutes about 5 wt. % to about 50 wt.
  • the second carbon inclusion constitutes at least 50 wt. % (e.g., at least 60 wt. %, at least 70 wt. %, at least 80 wt. %, at least 90 wt. %, at least 95 wt. %, or the like) of the second composition.
  • the weight ratio of active electrode material or active electrode material containing inclusions to first carbon inclusions, in a first fluid stock provided herein is at least 1 :4 (e.g., at least 1 :2 or 1 :2 to 10: 1). In more specific embodiments, the weight ratio is at least 1 : 1, e.g., at least 2: 1.
  • the weight ratio of active electrode material or active electrode material containing inclusions to overall carbon inclusions, including both the first and second carbon inclusions, in a film or combination of first and second compositions provided herein is at least 1 :4 (e.g., at least 1 :2). In more specific embodiments, the weight ratio is at least 1 : 1, e.g., at least 2: 1. In some embodiments, the weight ratio of active electrode material (or inclusions comprising the same) to overall carbon inclusions, including both the first and second carbon inclusions, in a film after reductive or thermal treatment is at least 1 : 1, e.g., at least 3 :2.
  • a first composition has a first average thickness
  • the second composition has a second average thickness, with the ratio of the first average thickness to the second average thickness being at least 1 : 1.
  • the ratio of the first average thickness to the second average thickness is at least 2: 1.
  • the ratio of the first average thickness to the second average thickness is at least 5: 1 (e.g., at least 10: 1).
  • the first composition is highly loaded on the substrate, such as having a loading by area (“areal loading") of at least 0.3 mg/cm 2 .
  • the loading of the first composition or domain is at least 0.5 mg/cm 2 , such as at least 1 mg/cm 2 .
  • the loading of the second composition or second domain is low (e.g., relative to the first composition or domain), such as having an areal loading of less than 0.3 mg/cm 2 .
  • the second composition or domain has an areal loading of about 0.001 mg/cm 2 to about 0.3 mg/cm 2 , such as about 0.005 mg/cm 2 to about 0.2 mg/cm 2 or about 0.01 mg/cm 2 to about 0.1 mg/cm 2 .
  • a film provided herein is a thin film, such as having an overall thickness (e.g., incorporating both the first and second domains or compositions, but not the substrate) of about 100 micron or less (e.g., about 50 micron or less, about 5 micron to about 25 micron, about 10 micron to 20 micron, or the like).
  • the film has an average thickness of about 5 micron to about 35 micron.
  • the first domain or composition has an average thickness of less than 25 micron (e.g., about 3 micron to about 25 micron).
  • the second domain has an average thickness of about 0.1 micron to about 10 micron.
  • the film has a thickness variation of less than 50%, e.g., less than 30%, less than 20%), less than 10%, or the like. Any suitable bulk density is contemplated, such as about 0.3 grams per cubic cm or more, such as about 0.5 grams per cubic cm or more.
  • a film provided herein has an externally exposed surface, the externally exposed surface comprising at least 90% (e.g., at least 95%, at least 97%, at least 98%), at least 99%, or the like) carbon inclusion (e.g., second and/or first carbon inclusion/component) by surface area.
  • less than 5% (e.g., less than 3%, less than 2%, less than 1%, or the like) of the surface of the film is comprised of the active electrode material.
  • the carbonaceous components constitute at least 70 wt. % of the film surface. In more specific embodiments, the carbonaceous components constitute at least 80 wt. % of the film surface. In still more specific embodiments, the carbonaceous components constitute at least 90 wt. % (e.g., at least 95 wt. %) of the film surface. In some embodiments, the active electrode material or active electrode material-containing inclusions constitute about 50 wt. % to about 95 wt. % of the film. In certain embodiments, the carbonaceous components constitute about 5 wt. % to about 50 wt. % of the film.
  • the one or more carbonaceous web provided therein defines a plurality of pockets with one or more of the particles (active electrode material containing inclusions) being configured therewithin.
  • the particles active electrode material containing inclusions
  • 1 ⁇ b ⁇ 20 wherein b is the average number of particles configured within the pocket(s) having particles configured therewithin.
  • the number of particles configured within the pockets can be higher.
  • values and characteristics described for individual components herein also include disclosure of such values and characteristics as an average of a plurality (i.e., more than one) of such components.
  • disclosure of average values and characteristics herein also includes a disclosure of an individual value and characteristic as applied to a single component herein.
  • FIG. 1 illustrates an electrode comprising a carbon web securing nanostructures on a substrate.
  • FIG. 2 shows an exemplary illustration of a gas controlled electrospray system and processes provided herein.
  • FIG. 3 shows an exemplary illustration of a process of a graphene component securing nanostructures to a substrate.
  • FIG. 4 shows an exemplary illustration of a plurality of carbon inclusions (graphene components) collectively forming a carbon web to secure nanostructures on a substrate.
  • FIG. 5 illustrates exemplary microscopic images of exemplary carbon webs securing active electrode components to a substrate.
  • FIG. 6 illustrates specific capacity data for various exemplary electrodes provided herein where the silicon particle composition is prepared without ball milling, with 30 minutes of ball milling, and with 2 hours of ball milling.
  • FIG. 7 illustrates exemplary reduced graphene oxide (rGO) structures.
  • FIG. 8 illustrates exemplary electrospray nozzle apparatuses utilized to manufacture certain electrodes and electrode materials provided herein.
  • FIG. 9 illustrates exemplary particles comprising active material and having low roundness in (a) pristine form, as well as (b) and (c) covered by carbon (at various zoom levels).
  • FIG. 10 illustrates the capacity retention of half cells prepared using exemplary anode materials described herein.
  • FIG. 11 illustrates the cycling efficiencies of half cells prepared using Si/C fiber anode materials.
  • FIG. 12 illustrates capacity retention and cycling efficiencies of full cells prepared using highly loaded, high sphericity anode materials described herein.
  • FIG. 13 illustrates exemplary graphene oxide (GO) structures.
  • Some embodiments provided herein describe a process for manufacturing an electrode or electrode material (e.g., for use in a lithium battery, such as a lithium ion or lithium sulfur battery).
  • Other embodiments provided herein describe compositions, films, and/or electrodes comprising a multi-domained structure, such as comprising plurality of silicon-containing particles and a plurality of grapheme components (e.g., for use as an electrode or electrode material described herein).
  • Silicon anodes are being developed for use in lithium batteries. Silicon has a larger energy density than currently used anode materials, but the large volume change of silicon when lithium is inserted is a major obstacle in commercializing lithium-silicon batteries.
  • silicon containing electrode materials suffer from poor performance characteristics, such as poor capacity retention on cycling, such as due to the formation of solid electrolyte interface (SEI) layers, pulverization, and the like.
  • silicon in a battery forms a solid electrolyte interface layer and this layer cracks and the silicon fragments and/or delaminates, limiting the number of charge/discharge cycling of the battery.
  • Spraying active electrode material containing inclusions (e.g., silicon particles) with a carbonaceous inclusion (e.g., graphene oxide) forms films with less silicon or other (non-graphitic/graphenic) active material on the surface, and the load of silicon can be increased without compromising battery performance.
  • additional spraying of a second material (e.g., graphene oxide) on top of the active electrode containing composition or domain further protects the active electrode material and increases cell performance, even while maintaining a constant overall active electrode material (e.g., silicon) loading.
  • a second material e.g., graphene oxide
  • the active electrode material e.g., silicon
  • the active (e.g., silicon) material becomes uncovered exposed to electrolyte, causing rapid decline in cell performance, such as through pulverization, SEI formation, fragmentation, delamination, or the like, limiting the battery's lifecycle.
  • Controlled and uniform systems whereby silicon materials are protected from adverse (e.g., SEI formation, pulverization, etc.) effects are desired (e.g., with carbon (e.g., graphene) components that envelope active electrode material (e.g., silicon and/or silicon oxide containing) particles, minimizing SEI formation and trapping active material particles, such as during cracking and/or breaking during lithiation/delithiation cycling).
  • active electrode material e.g., silicon and/or silicon oxide containing
  • a process for manufacturing an electrode, an electrode material, an electrode precursor, an electrode precursor material, and/or a part, composition, or domain thereof in certain embodiments, such processes involve generating a plume or aerosol in from a fluid stock comprising a plurality of inclusion components and a liquid medium.
  • generation of an electrode, electrode material, or active electrode part, composition, or domain thereof, or a precursor thereof comprises generating a plume or aerosol from a fluid stock comprising a plurality of inclusions and a liquid medium, the plurality of inclusions comprising a carbonaceous component (e.g., a grapheme component) and an active electrode component (e.g., particles comprising active electrode, such as SiOx).
  • a carbonaceous component e.g., a grapheme component
  • an active electrode component e.g., particles comprising active electrode, such as SiOx
  • generating a protective or top coat, part, composition, or domain of an electrode material, electrode, or precursor thereof comprises generating a plume or aerosol from a fluid stock comprising a plurality of inclusions and a liquid medium, the plurality of inclusions comprising a carbonaceous component (e.g., a grapheme component).
  • a carbonaceous component e.g., a grapheme component
  • processes herein comprise generating a first or base coat comprising an active material (e.g., inclusions comprising SiOx) and a carbonaceous component (e.g., a grapheme component, such as graphene oxide in precursor materials or reduced graphene oxide in electrode materials) and a protective or top coat comprising a carbonaceous component (e.g., a graphenic component, such as graphene oxide in precursor materials or reduced graphene oxide in electrode materials).
  • an active material e.g., inclusions comprising SiOx
  • a carbonaceous component e.g., a grapheme component, such as graphene oxide in precursor materials or reduced graphene oxide in electrode materials
  • a protective or top coat comprising a carbonaceous component (e.g., a graphenic component, such as graphene oxide in precursor materials or reduced graphene oxide in electrode materials).
  • a process for (i) generating a first plume or aerosol from a first fluid stock, the fluid stock comprising a conductive (e.g., carbon) inclusion (e.g., a graphene inclusion component) and an active electrode material (e.g., SiOx) inclusion and (ii) generating a second plume or aerosol form a second fluid stock, the second fluid stock comprising a conductive (e.g., carbon) inclusion (e.g., a graphene inclusion component) (e.g., in the absence of or at lower concentrations of an active electrode material).
  • a conductive e.g., carbon
  • an active electrode material e.g., SiOx
  • the first plume or aerosol is generated and deposited as a first (e.g., base) composition (or layer or domain) on a substrate, followed by the second plume or aerosol being generated and deposited on the first (e.g., base) composition (or layer or domain) as a second (e.g., top) composition (or layer or domain).
  • first e.g., base
  • second plume or aerosol being generated and deposited on the first (e.g., base) composition (or layer or domain) as a second (e.g., top) composition (or layer or domain).
  • the plumes or aerosols are generated using a suitable technique, such as an electrospray technique.
  • the process further comprises generating one or both of the plumes or aerosols in the presence of a high velocity gas.
  • the high velocity gas facilitates the fine dispersion of the plume or aerosol particulates, which, in turn, facilitates the controlled and uniform deposition of the inclusion parts on a substrate surface (e.g., the first composition forming a substrate surface for the second composition).
  • the direction of the flow of the gas and the plume/aerosol are in the same general direction (e.g., having a directional mean within 15 degrees, 10 degrees, 5 degrees, or the like of each other).
  • a fluid stock is electrosprayed with a gas (e.g., a controlled gas flow).
  • the fluid stock and the gas are ejected from an electrospray nozzle in a similar direction.
  • the direction of ejection of the fluid stock and the gas from the electrospray nozzle is within about 30 degrees of one another, or, more preferably within about 15 degrees of one another (e.g., within about 10 degrees or within about 5 degrees of one another).
  • the fluid stock and the gas are configured to be ejected from the nozzle in a coaxial or substantially coaxial configuration. In some instances, configurations and processes described herein allow for an enhanced driving force of electrospray, combining the driving forces of electric field gradient with high speed gas.
  • configurations provided herein allow for process throughput up to tens or hundreds of times greater than simple electrospray manufacturing and allow for the electrospray of high viscosity and/or highly loaded (e.g., with carbon and silicon inclusion materials described herein) fluids.
  • electrospray techniques and systems provided herein allow for the manufacture of highly uniform materials (e.g., compositions, films, electrodes, electrode materials, and electrode precursor materials).
  • other or conventional electrospray is not generally of commercial use in many applications because of, e.g., non-uniform deposition of drops and non-uniform dispersion of fillers in and between droplets, especially for high loaded systems.
  • electrospray techniques utilizing the fluid stocks and/or inclusions provided herein
  • electrospray techniques are optionally utilized in the manufacture of electrodes or depositions described herein, as applicable.
  • electrospray (e.g., using a process and/or system provided herein) of the fluid stock results in the formation of a plume comprising a plurality of droplets (collectively referred to herein so as to encompass, e.g., droplet solutions, droplet suspensions, and/or solid particles in an electrospray plume), or of a jet, which subsequently deforms into a plume comprising a plurality of droplets.
  • electrospray (e.g., using a process and/or system provided herein) of a fluid stock, such as provided herein results in the formation of a plume comprising a plurality of droplets.
  • the processes described herein results in the formation of small droplets (e.g., micron- or nano-scale droplets) having highly uniform size distributions (e.g., especially relative to standard electrospray techniques). In certain instances, this uniformity allows for much greater control of deposition formation, such as thickness, thickness uniformity, compositional uniformity (e.g., in composites), and the like.
  • films provided herein have an average thickness (d f ) that is about 10 mm or less, such as about 5 mm or less, about 2 mm or less, or about 1 mm or less.
  • the thickness of the film is about 500 micron (micrometer, ⁇ ) or less, such as about 250 micron or less, about 200 micron or less, about 100 micron or less, about or the like (e.g., down to about 1 micron, about 5 micron, about 10 micron, 25 micron, 50 micron, 100 micron, or the like).
  • the films provided herein have good thickness uniformity, such as wherein the thinnest portion of the film is > d f /10, > d f /5, > df/4, > d f /3, > d f /2, or the like.
  • the thickest portion of the film is ⁇ 10 x d f , ⁇ 5 x d f , ⁇ 3 x d f , ⁇ 2 x d f , ⁇ 1.5 x d f , ⁇ 1.2 x d f , or the like.
  • the minimum thickness of the film is greater than 0.9 d f , (more preferably greater than 0.95 d f ) and the maximum thickness of the film is less than 1.1 d f , (more preferably, less than 1.05 d f ).
  • FIG. 2 shows an exemplary illustration of a gas controlled electrospray system provided herein 200.
  • gas-controlled systems (and processes) provided herein provide electrospray (e.g., using V D C or VAC) of a fluid stock with a gas (illustrated by the downward arrows) 201 (e.g., having a controlled flow, such as circumferentially configured with the dispensing of the fluid stock) from a nozzle 202 (e.g., coaxially arranged, as illustrated in FIG. 2).
  • the droplets 203 proximal to the nozzle are smaller relative to non-gas controlled techniques (e.g., in some instances due to the controlled air flow at the nozzle end 204), and even smaller still as the droplets 205 move away from the nozzle toward the collector (droplets distal to the nozzle 206 and/or proximal to a collector 207).
  • such uniformity e.g., uniformity of size, horizontal distribution, etc.
  • dispersion of small droplets provides for a deposition 208 having a greatly improved uniformity of thickness, dispersion of inclusions, etc. As illustrated in FIG.
  • uniform dispersion of active materials and carbon materials in a fluid stock and resulting electrospray plume facilitate the deposition of a carbon material (e.g., graphene, GO, rGO sheet) 302 over a plurality of active material inclusions 303, thereby facilitating the wrapping of the active material inclusions 303 therein.
  • a carbon material e.g., graphene, GO, rGO sheet
  • further deposition of carbon materials 402 and active material inclusions 403 provides a layered electrode structure 405 comprising a plurality of active material inclusions 405 wrapped and/or secured within a web of the carbon material 402.
  • FIG. 4 illustrates a plurality of graphene envelopes comprising an external surface and an internal surface.
  • the graphene envelope optionally comprises one or more graphene component, such as illustrated in FIG. 4.
  • various graphene components of a composition described herein is a part of one or more graphene envelopes described herein.
  • the external surface of one graphene envelope, or a portion thereof optionally forms a portion of the internal surface of an adjacent graphene envelope.
  • the internal surface of a graphene envelope defines a graphene envelope pocket, such as illustrated in FIG. 4.
  • one or more particles comprising an electrode active material is configured within the graphene envelope pocket.
  • FIG. 5 illustrates images of exemplary electrodes provided herein comprising electrode active material wrapped within a carbon web - or a plurality of graphene envelopes with active electrode material configured therewithin (such as demonstrated by the illustration of FIG. 4).
  • such systems, processes and process steps are configured to facilitate high throughput electrospraying using a single or a banked nozzle system.
  • the systems and processes are configured for direct current voltage (V D C) or alternating current voltage (VAC) electrospraying, such as gas-controlled, direct current voltage or alternate current voltage (VAC) electrospraying.
  • V D C direct current voltage
  • VAC alternating current voltage
  • processes and systems provided herein are suitable for and/or configured to manufacture electrode precursor materials, electrode materials, uniform electrodes (e.g., on a current collector), such as having uniform thickness, capacity, component distribution, etc., or the like.
  • ejecting of a charged fluid stock from an electrospray nozzle produces a fluid jet, which is disrupted to form a plume comprising a plurality of droplets (or plume particulates).
  • droplets are in varying states of dryness (e.g., wherein more dry droplets comprise less fluid medium relative to solid inclusion materials) as they move toward a collector, with the droplets near the collector being dryer (i.e., comprising less fluid medium) (or even completely dry) than those droplets near the nozzle.
  • the plume comprises (e.g., especially in closest proximity to the collector substrate surface) droplets wherein all fluid medium has been evaporated.
  • a plume (or portion thereof) provided herein, comprises about 80 wt. % or less fluid, about 60 wt. % or less of a fluid, about 40 wt. % or less of a fluid, about 20 wt. % or less of a fluid, about 10 wt. % or less of a fluid, or about 5 wt. % or less of a fluid.
  • plume droplets (particularly in proximity to the collector substrate surface) are disrupted and small enough to reduce or minimize the number of inclusions included within each droplet. In certain instances, reducing and/or minimizing the number of inclusions in each droplets facilitates good distribution of inclusions throughout the plume, particularly in proximity to the collector. In some instances, good distribution of inclusions within the plume facilitates good distribution of inclusions as collected on the collector substrate.
  • processes and individual spray processing steps provided herein comprise generating a plume or aerosol (e.g., by electrospraying a fluid stock) with a high velocity gas (e.g., > 0.1 m/s, > 0.5 m/s, > 1 m/s, > 5 m/s, > 10 m/s, > 20 m/s, > 25 m/s, > 50 m/s, or other velocities provided herein).
  • a high velocity gas e.g., > 0.1 m/s, > 0.5 m/s, > 1 m/s, > 5 m/s, > 10 m/s, > 20 m/s, > 25 m/s, > 50 m/s, or other velocities provided herein.
  • a high velocity gas e.g., > 0.1 m/s, > 0.5 m/s, > 1 m/s, > 5 m/s, > 10 m/s, > 20 m/s, >
  • droplets of the plume comprise (e.g., on average) less than 100 inclusions (e.g., sum of active electrode material component inclusion(s) and graphene component inclusion(s) in the droplets), less than 50 inclusions, less than 20 inclusions, less than 10 inclusions or the like.
  • the collector is a distance d away from the electrospray nozzle and the droplets of the plume within d/2, d/3, or d/4 away from the collector comprise (e.g., on average) about 100 inclusions or less, about 50 inclusions or less, about 20 inclusions or less, about 10 inclusions or less, about 5 inclusions or less, about 3 inclusions or less, or the like.
  • the good dispersion of the droplets and the low concentration of inclusions per droplets facilitates the formation of a well -dispersed and well-controlled multi- component system, such as described herein.
  • a process provided herein comprises producing an electrostatically charged plume comprising a plurality of particles and/or droplets (e.g., an area or section of air comprising a plurality of particles and/or droplets dispersed therein).
  • the plurality of particles and/or droplets have an average diameter of about 500 micron or less, about 250 micron or less, about 100 microns or less, about 50 microns or less, less than 30 micron, about 20 microns or less, less than 15 micron, or about 10 microns or less.
  • the plurality of particles and/or droplets have an average diameter of about 5 microns or less, e.g., about 1 micron or less.
  • the size of the particles and/or droplets is highly uniform, with the standard deviation of the particle and/or droplet size being about 50% of the average size of the particles and/or droplets, or less (e.g., about 40% or less, about 30% or less, about 20% or less, about 10% or less, or the like) (e.g., at any given distance from the nozzle, e.g., about 10 cm or more, about 15 cm or more, about 20 cm or more, about 25 cm or more, from the nozzle).
  • electrospraying of a fluid stock or producing an electrostatically charged plume of a fluid stock comprises (i) providing a fluid stock to a first inlet of a first conduit of an electrospray nozzle, the first conduit being enclosed along the length of the conduit by a wall having an interior surface and an exterior surface, the first conduit having a first outlet; and (ii) providing a voltage to the electrospray nozzle (e.g., thereby providing an electric field).
  • a first fluid stock comprises a plurality (i.e., more than one) of active electrode material (e.g., silicon) containing particles, a plurality of carbon inclusions (e.g., (first) graphene components), and fluid medium (e.g., an aqueous medium, such as comprising water), and a second fluid stock comprises a plurality of carbon inclusions (e.g., (third) graphene components), and fluid medium (e.g., an aqueous medium, such as comprising water).
  • active electrode material e.g., silicon
  • fluid medium e.g., an aqueous medium, such as comprising water
  • second fluid stock comprises a plurality of carbon inclusions (e.g., (third) graphene components), and fluid medium (e.g., an aqueous medium, such as comprising water).
  • the plurality of active electrode material (e.g., silicon) containing particles have at least one average dimension (e.g., overall average dimension or average smallest dimension) of less than 100 micron ( ⁇ ) (e.g., about 0.5 micron to about 20 micron, such as about 1 micron to about 10 micron) (e.g., less than 50 micron, less than 20 micron, less than 10 micron, 0.2 micron to 10 micron, or less than 0.2 micron (200 nm)) (e.g., the smallest dimension).
  • ⁇ micron
  • ⁇ e.g., about 0.5 micron to about 20 micron, such as about 1 micron to about 10 micron
  • the carbon inclusion of the first and/or second fluid stock(s) and/or the collected (first and/or second) composition(s) are oxidized graphene components (e.g., graphene oxide).
  • the carbon inclusions (e.g., (first) graphene components) of the first and second fluid stocks (and/or compositions) independently comprise (e.g., on average) at least 50 wt. % carbon (e.g., about 60 wt. % to about 80 wt. % carbon).
  • the carbon inclusions (e.g., (first) graphene components) of the first and/or second fluid stocks and/or compositions independently comprise (e.g., on average) about 5 wt. % to about 50 wt. % oxygen (e.g., about 10 wt. % to about 40 wt. % oxygen).
  • individual droplets (generated from a fluid stock having an active electrode inclusion and a carbon inclusion) optionally comprise either or both of the active material and/or carbon inclusions.
  • some or all of the fluid of the droplets (of the plume) may be evaporated during the electrospray process (e.g., prior to deposition).
  • concentrations of inclusion materials in droplets described herein, or a composition comprising the same are generally higher than the concentrations of such materials in the fluid stock, or even in the jet (where evaporation of the fluid begins).
  • droplets or compositions comprising the droplets having inclusions concentrations of at least 1.5x, at least 2x, at least 3x, at least 5x, at least lOx, or the like (e.g., wherein the inclusions make up to 70 wt. % or more, 80 wt. % or more, 90 wt. % or more, or even 100 wt. % of the droplets or composition/plume comprising the same) of the concentrations of the fluid stock comprising the same.
  • a fluid stock (e.g., first and/or second fluid stock(s)) provided herein comprises at least 0.1 wt. % graphene component, at least 0.5 wt. % graphene component, or at least 1 wt. % graphene component, e.g., at least 2 wt.
  • the fluid stock(s) comprises about 2 wt. % to about 15 wt. % (e.g., about 10 wt. % to about 15 wt. %) graphene component.
  • a fluid stock is provided to a nozzle herein at any suitable flow rate, such as about 0.01 mL/min or more, about 0.05 mL/min or more, about 0.1 mL/min or more, about 0.2 mL/min or more, or about 0.01 mL/min to about 10 mL/min.
  • the controlled air flow allows for an increase rate and uniformity in dispersion and breaking up of the jet and the plume, allowing for increased fluid stock flow rates, while also increasing deposition uniformity and performance characteristics.
  • the fluid stock is provided to the first inlet at a rate (e.g., where a direct current voltage (V D C) is applied to the electrospray system) of about 0.01 to about 10 mL/min, e.g., about 0.05 mL/min to about 5 mL/min, or about 0.5 mL/min to about 5 mL/min.
  • the fluid stock is provided to the first inlet at a rate of about 0.1 mL/min or more, e.g., about 0.1 mL/min to about 25 mL/min, about 0.3 mL/min or more, about 0.5 mL/min or more, about 1 mL/min or more, about to about 2.5 mL/min, or about 5 mL/min or more.
  • a process described herein comprises providing a fluid stock to a first inlet of a first conduit of an electrospray nozzle, the first conduit being enclosed along the length of the conduit by a wall having an interior surface and an exterior surface, the first conduit having a first outlet.
  • the walls of the first conduit form a capillary tube, or other structure.
  • the first conduit is cylindrical, but embodiments herein are not limited to such configurations.
  • FIG. 8 illustrates exemplary electrospray nozzle apparatuses 800 and 830 provided herein. Illustrated by both nozzle components 800 and 830 some embodiments, the nozzle apparatus comprises a nozzle component comprising a first (inner) conduit, the first conduit being enclosed along the length of the conduit by a first wall 801 and 831 having an interior and an exterior surface, and the first conduit having a first inlet (or supply) end 802 and 832 (e.g., fluidly connected to a first supply chamber and configured to receive a fluid stock) and a first outlet end 803 and 833. Generally, the first conduit has a first diameter 804 and 834 (e.g., the average diameter as measured to the inner surface of the wall enclosing the conduit).
  • a first diameter 804 and 834 e.g., the average diameter as measured to the inner surface of the wall enclosing the conduit.
  • the nozzle component comprising a second (outer) conduit, the second conduit being enclosed along the length of the conduit by a second wall 805 and 835 having an interior and an exterior surface, and the second conduit having a second inlet (or supply) end 806 and 836 (e.g., fluidly connected to a second supply chamber and configured to receive a gas - such as a high velocity or pressurized gas (e.g., air)) and a second outlet end 807 and 837.
  • a gas - such as a high velocity or pressurized gas (e.g., air)
  • the second inlet (supply) end 806 and 836 is connected to a supply chamber.
  • the second inlet (supply) end 806 and 836 are connected to the second supply chamber via a supply component.
  • connection supply component e.g., tube
  • inlet supply component 815 and 845 which is fluidly connected to the inlet end of the conduit.
  • the figure illustrates such a configuration for the outer conduit, but such a configuration is also contemplated for the inner and any intermediate conduits as well.
  • the first conduit has a first diameter 808 and 838 (e.g., the average diameter as measured to the inner surface of the wall enclosing the conduit).
  • the first and second conduits have any suitable shape.
  • the conduits are cylindrical (e.g., circular or elliptical), prismatic (e.g., an octagonal prism), conical (e.g., a truncated cone - e.g., as illustrated by the outer conduit 835) (e.g., circular or elliptical), pyramidal (e.g., a truncated pyramid, such as a truncated octagonal pyramid), or the like.
  • the conduits are cylindrical (e.g., wherein the conduits and walls enclosing said conduits form needles).
  • the walls of a conduit are parallel, or within about 1 or 2 degrees of parallel (e.g., wherein the conduit forms a cylinder or prism).
  • the nozzle apparatus 800 comprise a first and second conduit having parallel walls 801 and 805 (e.g., parallel to the wall on the opposite side of the conduit, e.g., as illustrated by 801a / 801b and 805a / 805b, or to a central longitudinal axis 809).
  • the walls of a conduit are not parallel (e.g., wherein the diameter is wider at the inlet end than the outlet end, such as when the conduit forms a cone (e.g., truncated cone) or pyramid (e.g., truncated pyramid)).
  • the nozzle apparatus 830 comprise a first conduit having parallel walls 831 (e.g., parallel to the wall on the opposite side of the conduit, e.g., as illustrated by 83 la / 83 lb, or to a central longitudinal axis 839) and a second conduit having non-parallel walls 835 (e.g., not parallel or angled to the wall on the opposite side of the conduit, e.g., as illustrated by 835a / 835b, or to a central longitudinal axis 839).
  • the walls of a conduit are within about 15 degrees of parallel (e.g., as measured against the central longitudinal axis, or half of the angle between opposite sides of the wall), or within about 10 degrees of parallel.
  • the walls of a conduit are within about 5 degrees of parallel (e.g., within about 3 degrees or 2 degrees of parallel).
  • conical or pyramidal conduits are utilized.
  • the diameters for conduits not having parallel walls refer to the average width or diameter of said conduit.
  • the angle of the cone or pyramid is about 15 degrees or less (e.g., the average angle of the conduit sides/walls as measured against a central longitudinal axis or against the conduit side/wall opposite), or about 10 degrees or less.
  • the angle of the cone or pyramid is about 5 degrees or less (e.g., about 3 degrees or less).
  • the first conduit 801 and 831 and second conduit 805 and 835 having a conduit overlap length 810 and 840, wherein the first conduit is positioned inside the second conduit (for at least a portion of the length of the first and/or second conduit).
  • the exterior surface of the first wall and the interior surface of the second wall are separated by a conduit gap 811 and 841.
  • the first outlet end protrudes beyond the second outlet end by a protrusion length 812 and 842.
  • the ratio of the conduit overlap length-to- second diameter is any suitable amount, such as an amount described herein.
  • the ratio of the protrusion length-to-second diameter is any suitable amount, such as an amount described herein, e.g., about 1 or less.
  • FIG. 8 also illustrates cross-sections of various nozzle components provided herein 850, 860 and 870.
  • Each comprises a first conduit 851, 861 and 871 and second conduit 854, 864, and 874.
  • the first conduit is enclosed along the length of the conduit by a first wall 852, 862 and 872 having an interior and an exterior surface and the second conduit is enclosed along the length of the conduit by a second wall 855, 865 and 875 having an interior and an exterior surface.
  • the first conduit has any suitable first diameter 853, 863 and 864 and any suitable second diameter 856, 866, and 876.
  • the cross- dimensional shape of the conduit is any suitable shape, and is optionally different at different points along the conduit.
  • coaxially configured nozzles provided herein and coaxial gas controlled electrospraying comprises providing a first conduit or fluid stock along a first longitudinal axis, and providing a second conduit or gas (e.g., pressurized or high velocity gas) around a second longitudinal axis (e.g., and electrospraying the fluid stock in a process thereof).
  • a second conduit or gas e.g., pressurized or high velocity gas
  • the first and second longitudinal axes are the same. In other embodiments, the first and second longitudinal axes are different.
  • the first and second longitudinal axes are within 500 microns, within 100 microns, within 50 microns, or the like of each other. In some embodiments, the first and second longitudinal axes are aligned within 15 degrees, within 10 degrees, within 5 degrees, within 3 degrees, within 1 degree, or the like of each other.
  • FIG. 8 illustrates a cross section of a nozzle component 870 having an inner conduit 871 that is off-center (or does not share a central longitudinal axis) with an outer conduit 874.
  • the conduit gap (e.g., measurement between the outer surface of the inner wall and inner surface of the outer wall) is optionally averaged - e.g., determined by halving the difference between the diameter of the inner surface of the outer wall 876 and the diameter of the outer surface of the inner wall 872.
  • the smallest distance between the inner surface of the outer wall 876 and the diameter of the outer surface of the inner wall 872 is at least 10% (e.g., at least 25%, at least 50%), or any suitable percentage) of the largest distance between the inner surface of the outer wall 876 and the diameter of the outer surface of the inner wall 872.
  • a process herein comprises or a system provided herein is configured to provide a voltage (e.g., V D C or VAC) to an electrospray nozzle, such as one provided herein.
  • a voltage e.g., V D C or VAC
  • the voltage is provided to the inner conduit (e.g., the walls thereof).
  • application of the voltage to the nozzle provides an electric field at the nozzle (e.g., at the outlet of the inner conduit thereof).
  • the electric field results in the formation of a "cone” (e.g., Taylor cone) at the nozzle (e.g., at the outlet of the inner conduit thereof), and ultimately a jet and/or a plume.
  • a "cone” e.g., Taylor cone
  • the jet and/or plume is broken up into small and highly charged liquid droplets (or particles), which are dispersed, e.g., due to Coulomb repulsion.
  • droplets and particles are referred to interchangeably, wherein the particles comprise droplets (e.g., comprising a liquid medium of the fluid stock) or dried particles (e.g., wherein the liquid medium of the fluid stock has been evaporated during the electrospray process).
  • any suitable voltage e.g., direct or alternating current voltage
  • the voltage applied is about 8kV D c to about 30 kV D c, e.g., about 10 kV D c to about 25 kV D c-
  • the voltage applied is about 10 kVAc (e.g., wherein the voltage refers to the root mean square voltage (Vrms)) or more.
  • the voltage applied is about 20 ICVAC or more, e.g., about 30 ICVAC or more.
  • the voltage applied is about 10 ICVAC to about 25 ICVAC-
  • a power supply system is configured to provide the voltage to the nozzle.
  • the alternating voltage (VAC) has any suitable frequency, such as about 25 Hz or more, e.g., about 50 Hz to about 500 Hz. In more specific embodiments, the frequency is about 60 Hz to about 400 Hz, e.g., about 60 Hz to about 120 Hz, or about 60 Hz to about 250 Hz.
  • the voltage applied to a nozzle is about 8 kV D c to about 30 kV D c- In specific embodiments, the voltage applied to the nozzle is about 10 kVoc to about 25 kVoc- In other embodiments, the voltage applied to the nozzle is about 10 kV A c or more (e.g., about 15 kV A c or more, or about 20 kV A c to about 25 kV A c)- In some embodiments, the alternating voltage (VAC) has a frequency of about 50 Hz to about 350 Hz.
  • a process herein provides a pressurized gas to an outer inlet of an outer conduit of an electrospray nozzle.
  • the outer conduit is enclosed along the length of the conduit by an outer wall having an interior surface, the outer conduit having an outer conduit inlet and an outer conduit outlet.
  • the pressurized gas is provided from a pressurized canister, by a pump, or by any other suitable mechanism. Generally, providing pressurized gas to the inlet of the outer channel results in a high velocity gas being discharged from the outlet of the outer channel of the electrospray nozzle.
  • any suitable gas pressure or gas velocity is optionally utilized in processes and/or systems herein.
  • the gas pressure applied e.g., to the inlet of the outer channel
  • the gas pressure is about 20 psi or more, about 25 psi or more, about 35 psi or more, about 45 psi or more, or any other suitable pressure.
  • the velocity of the gas at the nozzle is about 0.5 m/s or more, about 1 m/s or more, about 5 m/s or more, about 10 m/s or more, about 25 m/s or more.
  • the velocity is about 50 m/s or more. In still more specific embodiments, the velocity is about 100 m/s or more, e.g., about 200 m/s or more, or about 300 m/s.
  • the gas is any suitable gas, such as comprising air, oxygen, nitrogen, argon, hydrogen, or a combination thereof.
  • the inner and outer conduits have any suitable diameter.
  • the diameter of the outer conduit is about 0.1 mm to about 10 mm, e.g., about 1 mm to about 10 mm.
  • the diameter of the outer conduit is about 0. 1 mm to about 5 mm, e.g., about 1 mm to about 3 mm.
  • the diameter of the inner conduit is about 0.01 mm to about 8 mm, e.g., about 0.5 mm to about 5 mm, e.g., about 1 mm to about 4 mm.
  • the inner conduit is configured inside the outer conduit, preferably along an identical axis, but slight offset configurations are also considered to be within the scope of the instant disclosure.
  • an outer wall surrounds the outer conduit, the outer wall having an interior surface (e.g., defining the outer conduit).
  • the average distance between the exterior surface of the inner wall and the interior surface of the outer wall is any suitable distance.
  • the conduit gap is about 0.1 mm or more, e.g., about 0.5 mm or more, or about 1 mm or more. In certain embodiments, the gap is small enough to facilitate a high velocity gas at the nozzle and to facilitate sufficient disruption of the charged fluid (jet) ejected from the nozzle (e.g., such as to provide sufficiently small droplet sizes and sufficiently uniform inclusion dispersion in the plume and on the collection substrate). In some embodiments, the conduit gap is about 0.01 mm to about 30 mm, such as about 0.05 mm to about 20 mm, about 0.1 mm to about 10 mm, or the like. In more specific embodiments, the conduit gap is about 0.5 mm to about 5 mm.
  • the inner conduit and the outer conduit run along an identical or similar longitudinal axis, the length of which both the inner and outer conduit running along that axis being the conduit overlap length.
  • the inner conduit length, the outer conduit length, and the conduit overlap length is about 0.1 mm or more, e.g., about 0.1 mm to about 100 mm, or more.
  • the inner conduit length, the outer conduit length, and the conduit overlap length is about 0.5 mm to about 100 mm, e.g., about 1 mm to about 100 mm, about 1 mm to about 50 mm, about 1 mm to about 20 mm, or the like.
  • the ratio of the conduit overlap length to the first diameter being about 1 to about 100 (e.g., about 10), or about 0.1 to about 10, e.g., about 0.1 to about 5 or about 1 to about 10.
  • the inner conduit is longer than the outer conduit, the inner conduit protruding beyond the outer conduit, e.g., as illustrated in FIG. 8.
  • the protrusion length is about -0.5 mm to about 1.5 mm, e.g., about 0 mm to about 1.5 mm, or about 0 mm.
  • processes herein comprise collecting and/or systems herein are configured to collect small particles and/or droplets of the plume onto a substrate.
  • collection of these small particles/droplets allows for the formation of a uniform deposition on the substrate.
  • the substrate is positioned opposite the outlet of the nozzle.
  • processes provided herein comprise collecting a first composition (e.g., a deposition or film (e.g., a film being a layer of material, such as prepared by a deposition technique described herein) resulting from the electrospraying of a first fluid stock as described herein) on a substrate (e.g., metal foil), and collecting a second composition (e.g., resulting from electrospraying of a second fluid stock as described herein) on the first composition.
  • a first composition e.g., a deposition or film (e.g., a film being a layer of material, such as prepared by a deposition technique described herein) resulting from the electrospraying of a first fluid stock as described herein
  • a substrate e.g., metal foil
  • a second composition e.g., resulting from electrospraying of a second fluid stock as described herein
  • the first composition or deposition, or combination of first and second composition e.g., a precursor for an electrode or electrode material described herein
  • first and second composition comprises a plurality of active electrode material (e.g., silicon) containing particles and a plurality of carbon inclusions (e.g., (first) graphene components), such as described in the fluid stock herein.
  • the fluid of the fluid stock(s) is partially or completely removed (e.g., by evaporation during the electrospray process).
  • the composition(s) or deposition(s), or combination of first and second compositions comprise a plurality of the active electrode containing inclusions (e.g., SiOx particles, such as microparticles described herein) secured within a carbonaceous web, such as a graphenic web comprising a plurality of graphenic inclusion components.
  • inclusions e.g., SiOx particles, such as microparticles described herein
  • the substrate is a grounded substrate or positioned between a plume generating nozzle and a grounded surface.
  • the substrate has a surface that is positioned in opposing relation to a plume generating nozzle outlet (e.g., there is "line of sight" between the nozzle outlet and the substrate surface).
  • the opposing substrate is directly opposing the nozzle (e.g., configured orthogonal to nozzle conduit configuration, such as illustrated in FIG. 2).
  • the opposing substrate is angled or offset from directly opposing the nozzle.
  • the substrate is affixed to or is a part of a conveyor system.
  • the substrate is attached to a conveyor belt or is a part of a conveyor belt.
  • the substrate is a metal (e.g., a foil, such as of copper, aluminum, or the like) or other current collector type material (e.g., wherein a process herein is utilized to manufacture an anode material directly on a current collector), or on a substrate from which the electrode material is readily removed (e.g., wherein a process herein is utilized to manufacture anode powder materials).
  • processes provided herein further comprise chemically and/or thermally treating a collected composition (e.g., such as to at least partially de-oxygenate the highly oxygenated first graphene component (e.g., graphene oxide)), or otherwise subjecting the collected composition to reductive conditions (e.g., suitable to reduce an oxygenated graphenic component).
  • a process described herein comprises thermally treating (e.g., to at least 100 °C) a collected composition to provide a treated composition.
  • the treated composition comprises a plurality of active electrode material (e.g., silicon) containing particles and a plurality of carbon inclusions (e.g., (second) graphene components), wherein the carbon inclusions of the treated composition comprise a greater weight percentage of carbon and a lower weight percentage of oxygen than do the carbon inclusions of the fluid stock.
  • the carbon inclusions of the treated composition are oxidized graphene components that have been reduced.
  • the carbon inclusions (e.g., treated graphene components) of the (e.g., thermally) treated composition comprise about 90 wt. % or more carbon and about 0.1 wt. % to about 10 wt. % oxygen.
  • chemical and/or thermal treatment is optionally performed while the collected composition is on the substrate, or after removal of the collected composition from the substrate.
  • the first (active electrode material containing or base) composition is treated prior to or following deposition of the second (or top, e.g., non-active electrode or silicon material containing) composition thereon.
  • a film comprising both the first and second composition is treated.
  • a process herein comprises a step of reducing the graphene component (e.g., decreasing the oxygen content thereof). In some embodiments, a process herein comprises thermally or chemically or otherwise reducing the graphene component. In certain embodiments, the reduced graphene component is a reduced graphene oxide. In some embodiments, the reduced graphene component or reduced graphene oxide is a graphene (pristine or defective, such as comprising one or more opened internal rings, or the like) that is optionally functionalized with oxygen, such as described for graphene oxides (e.g., wherein the oxygen wt. % is less than the oxygen wt. % of the graphene component of the fluid stock).
  • reduced graphene component e.g., reduced graphene oxide (rGO)
  • rGO reduced graphene oxide
  • thermal e.g., heating, such as to 200 °C or more, such as under inert (e.g., nitrogen, argon, etc. atmosphere) or reductive conditions (e.g., hydrogen gas, mixed inert and hydrogen gas, or the like)
  • irradiation e.g., hydrogen gas, mixed inert and hydrogen gas, or the like
  • chemical e.g., by treating with hydrazine, hydrogen plasma, urea, or the like
  • other e.g., using strong pulse light
  • FIG. 7 illustrates various exemplary reduced graphene oxide (rGO) structures.
  • the structure may have a basic two dimensional honeycomb lattice structure of graphene, with (or without) defects and with (or without) other atoms present (e.g., hydrogen and/or oxygen, including, e.g., oxidized structures, such as discussed and illustrated herein).
  • the reduced graphene component or reduced graphene oxide comprises about 60% or more carbon (e.g., 60% to 99%), such as about 70 wt. % or greater, about 75 wt. % or more, about 80 wt. % or greater, about 85 wt. % or greater, about 90 wt. % or greater, or about 95 wt. % or greater (e.g., up to about 99 wt.
  • the reduced graphene component (e.g., rGO) comprises about 35 wt. % or less (e.g., 0.1 wt. % to 35 wt. %) oxygen, e.g., about 25 wt. % or less (e.g., 0.1 wt. % to 25 wt. %) oxygen, or about, about 20 wt. % or less, about 15 wt. % or less, about 10 wt. % or less (e.g., down to about 0.01 wt. %, down to about 0.1 wt. %, down to about 1 wt. % or the like) oxygen.
  • the reduced graphene component (e.g., rGO) comprises about 0.1 wt. % to about 10 wt. % oxygen, e.g., about 4 wt. % to about 9 wt. %, about 5 wt, % to about 8 wt, %, or the like.
  • the total percentage of carbon and oxygen does not constitute 100% of the reduced graphene component, with the additional mass comprising any suitable atoms, such as hydrogen, or other agents, as discussed for the non- reduced graphene components herein.
  • a graphene component e.g., graphene oxide
  • the collected deposition is thermally treated (e.g., to a temperature of about 100 °C or more, e.g., about 150 °C to about 350 °C, about 200 °C to about 300 °C, about 200 °C, about 250 °C, or any suitable temperature), such as to at least partially reduce the graphene oxide (i.e., decrease the percentage of oxygen relative to carbon in the graphene oxide).
  • thermal treatment of the graphene web shrinks the graphene web around the particles enclosed within the graphene pocket.
  • the shrunk web further protects the particles therewithin (e.g., by further minimizing electrolyte interaction with the particle), such as by reducing or minimizing the space within the envelope in which electrolyte can be trapped.
  • the pocket such as the shrunk pocket, retains its flexibility, allowing the particles to expand (e.g., up to at least 200% the original volume, at least 300% the original volume, at least 400% the original volume, or the like), such as within the pocket (e.g., allowing the particles to expand without becoming unnecessarily exposed to electrolyte, which can react with silicon to form a detrimental SEI layer when the silicon is lithiated).
  • the void space volume (volume within envelope not taken up by particles therewithin) within the shrunk pocket is reduced (e.g., relative to the pre-thermally treated envelope) by at least 10%, at least 20%, at least 30%), at least 50%>, or the like following thermal treatment of the web.
  • the void space volume within the pocket is any suitable volume, such as less than 100%), less than 50%>, less than 25%>, less than 10%>, or the like of the volume of the particles therein.
  • any other suitable technique is optionally utilized to reduce the graphene oxide following deposition. In some instances, reduction of the graphene oxide following deposition improve the performance characteristics of the material (e.g., by, in some instances, increasing conductivity of the carbon inclusion).
  • various figures provided herein illustrate that in some instances, materials provided herein demonstrate improved performance (e.g., specific capacity) characteristics with reduced graphene oxide (rGO), relative to graphene oxide (GO).
  • rGO reduced graphene oxide
  • GO graphene oxide
  • processes herein omit the reduction steps, such as wherein a graphene component suitable for an electrode material is utilized directly in the fluid stock.
  • an electrospray process described herein is a gas assisted or gas controlled electrospray process.
  • a fluid stock provided herein is electrosprayed with a gas stream.
  • a fluid stock described herein is injected into a gas stream during electrospraying.
  • a process of producing of an electrostatically charged plume from a fluid stock further comprises providing a pressurized gas to a second inlet of a second conduit of a nozzle described herein.
  • the second conduit has a second inlet and a second outlet, and at least a portion of the first conduit being positioned inside the second conduit (i.e., at least a portion of the second conduit being positioned in surrounding relation to the first conduit).
  • the gap between the outer wall of the inner conduit and the inner wall of the outer conduit is small enough to facilitate a high velocity gas at the nozzle, such as to facilitate sufficient disruption of the charged fluid (jet) ejected from the nozzle (e.g., such as to provide plume or aerosol dispersions described herein).
  • the conduit gap is about 0.01 mm to about 30 mm, such as about 0.05 mm to about 20 mm, about 0.1 mm to about 10 mm, or the like.
  • the gas stream (e.g., at the second outlet) has a high velocity, such as a velocity of at least 1 m/s, e.g., at least 5 m/s, at least 10 m/s, at least 20 m/s, or more.
  • a process provided herein comprises compressing of a collected and/or (e.g., thermally) treated composition or film described herein.
  • a collected and/or (e.g., thermally) treated composition or film is compressed such as to provide a compressed composition having a density of about 0.4 g per cubic centimeter (g/cc) or greater, such as about 0.5 g/cc or greater, or about 0.5 g/cc to about 2 g/cc (e.g., 0.7 g/cc to 2 g/cc) (e.g., about 1 g/cm 3 or more, about 1.5 g/cm 3 or more, or the like).
  • a collected, (e.g., thermally) treated, and/or compressed composition or film has a thickness of about 1 mm or less, or about 200 micron or less (e.g., on the substrate).
  • a process provided herein further comprises compressing (e.g., calendering or otherwise compressing) a film or deposition provided herein.
  • compression of the deposition provides increased electrode density and/or a thinner electrode, which, in some instances, provides improved volumetric energy density of the electrode.
  • volumetric energy density of the electrode is improved by at least 1.1 times, e.g., about 1.2x or more, about 1.25x or more, or about 1.5x or more, such as up to about 2x or more.
  • volumetric energy density (of the anode) provided herein is about 500 mAh/cubic cm (cc) or more, such as about 750 mAh/cc or more, about 1000 mAh/cc or more, or the like.
  • such a compression step is utilized when electrode active material (e.g., comprising SiOx) structures are micron scale (e.g., that is about 1 micron or greater, such as about 2 micron or greater, or about 2 micron to about 100 micron, or as otherwise described herein) dimension (or, e.g., an average dimension).
  • electrode active material e.g., comprising SiOx
  • micron scale e.g., that is about 1 micron or greater, such as about 2 micron or greater, or about 2 micron to about 100 micron, or as otherwise described herein
  • compression of electrode materials comprising active electrode materials of the micron scale are particularly useful in increasing density of the material as the micron scaled structures can leave larger voids during deposition (e.g., relative to nanoscaled structures).
  • the film or deposition is compressed to a thickness about 90% or less, about 80% or less, about 70% or less, about 60% or less, or about 50% or less of the pre-compressed deposition thickness.
  • an electrode or electrode material
  • the electrode comprising (a) an inclusion (e.g., micro- and/or nano- structured) comprising an active material (e.g., electrode active material, such as silicon) and (b) a carbon (or carbonaceous) component (e.g., referred to interchangeably herein as a carbon inclusion).
  • the process comprises producing a first and second electrostatically charged plume comprising a plurality of (e.g., micro- and/or nano-scale) particles and/or droplets from a first and a second fluid stock, such as described herein.
  • such plumes are prepared by providing a fluid stock to an inlet of a conduit of an electrospray nozzle (e.g., and applying a voltage to the electrospray nozzle).
  • the process comprises applying a voltage to the nozzle (e.g., wall of the conduit).
  • the voltage provides an electric field (e.g., at an outlet of the nozzle conduit, such as to expel the fluid stock as a jet and/or plume from the nozzle, e.g., outlet thereof).
  • the conduit is enclosed along the length of the conduit by a wall having an interior surface and an exterior surface, the conduit having an outlet.
  • a first fluid stock comprising a (e.g., nanostructured) inclusion comprising an active material (e.g., an electrode active material), a carbon inclusion, and a liquid medium (e.g., water).
  • a second fluid stock comprises a carbon inclusion.
  • the process further comprises collecting a first and second deposition, composition or layer (e.g., collectively as a film) on a substrate (e.g., a conducting substrate, such as a current collector described herein).
  • the film comprises (a) an inclusion comprising an active material and (b) a carbon component (e.g., a carbon web, such as securing (e.g., wrapping, trapping, and/or enveloping) the inclusion materials (e.g., nanostructured inclusion materials) comprising the active material therein).
  • a carbon component e.g., a carbon web, such as securing (e.g., wrapping, trapping, and/or enveloping) the inclusion materials (e.g., nanostructured inclusion materials) comprising the active material therein.
  • the film comprises a top coat comprising a carbon component, such as described herein, the topcoat being free or substantially free of the active (e.g., silicon) material.
  • a film or deposition provided herein is a thin layer film or deposition, e.g., having an average thickness of about 1 mm or less, e.g., about 1 micron to about 1 mm.
  • the deposition has a thickness of about 500 micron or less, e.g., about 1 micron to about 500 micron, about 1 micron to about 250 micron, or about 10 micron to about 200 micron, about 20 micron or less, about 0.5 micron to about 20 micron, or the like.
  • the processes and systems described herein not only allow for the manufacture of thin layer depositions, but of highly uniform thin layer films or depositions.
  • the films or depositions provided herein have an average thickness, wherein the thickness variation is less than 50% of the average thickness, e.g., less than 30% of the average thickness, or less than 20% of the average thickness.
  • the substrate is any suitable substrate (e.g., a grounded substrate, or a substrate located between the electrospray nozzle and a grounded plate).
  • the substrate is a current collector material (e.g., a metal, such as copper or aluminum, foil or sheet).
  • any reductive (e.g., thermal reductive) treatment is optionally performed without removing the deposited material from the substrate.
  • compositions or electrodes comprising an electrode material, or precursor thereof, and a substrate, such as described herein (e.g., a conductive substrate, such as a metal - e.g., an aluminum or copper foil).
  • a substrate such as described herein (e.g., a conductive substrate, such as a metal - e.g., an aluminum or copper foil).
  • a fluid stock (e.g., for electrospraying) provided herein comprises any suitable components.
  • the fluid stock comprises a liquid medium and one or more inclusion component.
  • a fluid stock for forming a base coat comprises a liquid medium, an active electrode material, or a precursor thereof, and a carbon material (e.g., a carbon inclusion, such as a graphene component, described herein), and a fluid stock for forming a top coat comprises a liquid medium, and a carbon material (e.g., a carbon inclusion, such as a graphene component, described herein).
  • Other additional inclusion materials are optionally included in either or both fluid stock.
  • any suitable fluid stock is utilized in a process provided herein.
  • an active-electrode material containing fluid stock comprises less than 30 wt. % active electrode material (e.g., silicon) containing particles.
  • the fluid stock comprises less than 20 wt. % active electrode material (e.g., silicon) containing particles.
  • the first fluid stock comprises about 0.2 wt. % to about 10 wt. % active electrode material (e.g., silicon) containing particles.
  • electrospray processes occur with a gas stream, higher loading of particles and/or carbon inclusions are possible.
  • the active-electrode material containing fluid stock comprises about 1 wt. % or more (e.g., about 2.0 wt. % or more) active electrode material (e.g., silicon) containing particles.
  • the fluid stock comprises about 5 wt. % or more active electrode material (e.g., silicon) containing particles.
  • the active-electrode material containing fluid stock comprises about 5 wt. % to about 20 wt. % active electrode material (e.g., silicon) containing particles.
  • the weight ratio of active electrode material (e.g., silicon) containing particles to carbon inclusion (e.g., graphene components) in the active- electrode material containing fluid stock or other composition (e.g., first layer or composition of a film) herein (e.g., collected and/or thermally treated films or first compositions, domains, or layers) is at least 1 : 10, e.g., at least 1 :5, at least 1 :3, at least 1 :2, at least 2:3, at least 1 : 1, at least 3 :2, or at least 2: 1 (e.g., up to 10: 1 or up to 20: 1).
  • the weight ratio of active electrode material (e.g., silicon) containing particles to carbon inclusion (e.g., graphene components) is about 1 : 10 to about 10: 1, about 1 :3 to about 5: 1, about 1 :2 to about 3 : 1, about 2:3 to about 2: 1, or the like (e.g., in the first composition, overall film, and/or first fluid stock herein). In more specific embodiments, the ratio is at least 2:3, at least 1 : 1, or the like. In certain embodiments, at least 50 wt. % of the solid particulates included in the first fluid stock comprise active electrode material particulate inclusions and grapheme inclusions (graphene component). In specific embodiments, at least 70 wt.
  • active electrode material e.g., silicon
  • carbon inclusion e.g., graphene components
  • the solid particulates included in the active-electrode material containing fluid stock comprise active electrode material particulate inclusions and carbonaceous (e.g., grapheme) inclusions.
  • at least 95 wt. % of the solid particulates included in the first fluid stock comprise active electrode material particulate inclusions and grapheme inclusions.
  • similar or identical ratios of active material to carbon inclusion are provided herein for the materials and electrodes described herein, though in some instances wherein the carbon inclusion material (e.g., graphene component) is reduced, higher ratios are also contemplated for electrodes and electrode materials herein due to the weight loss resulting from the reduction process (e.g., due to the removal of oxygen from the carbon inclusion material). In preferred embodiments, higher ratios of active material to carbon material are preferred in order to improve the capacity of the resultant electrode materials, while not increased to such an extent so as to overly diminish cell cycling performance (e.g., by providing an insufficient amount of carbon inclusion material to sufficiently protect the active electrode material, such as from SEI formation, pulverization, or the like).
  • the carbon inclusion material e.g., graphene component
  • higher ratios of active material to carbon material are preferred in order to improve the capacity of the resultant electrode materials, while not increased to such an extent so as to overly diminish cell cycling performance (e.g., by providing an insufficient amount of carbon inclusion material to
  • Carbon inclusions e.g., graphene components
  • active material or precursors thereof
  • concentrations are preferred that increase or maximize throughput capabilities, while avoiding clogging the nozzle systems and/or causing unwanted aggregation, clumping, etc. of inclusion materials.
  • graphene components are included in the fluid stock in an amount sufficiently low to allow good dispersion and unpacking of the graphene sheets (e.g., to reduce or minimize folding of the graphene sheets onto one another).
  • either fluid stock independently comprises about 0.01 wt.
  • the base coat fluid stock comprises about 0.01 wt. % or more active material (e.g., silicon-containing particles). In more specific embodiments, either fluid stock independently comprises about 0.1 wt. % to about 10 wt. % carbon inclusion (e.g., graphene component, such as GO). In some embodiments, either fluid stock independently comprises about 1 wt. % to about 5 wt. % carbon inclusion (e.g., graphene component, such as GO). In more specific embodiments, the base coat fluid stock comprises about 0.1 wt. % to about 30 wt. % active material (e.g., silicon-containing particles).
  • active material e.g., silicon-containing particles
  • the base coat fluid stock comprises about 0.2 wt. % to about 20 wt. % (e.g., about 0.2 wt. % to about 10 wt. %) active material (e.g., silicon-containing particles). In some embodiments, the base coat fluid stock comprises about 1 wt. % to about 15 wt. % (e.g., about 5 wt. % to about 10 wt. %) active material (e.g., silicon-containing particles).
  • the concentration of the electrode active material and/or inclusions comprising the electrode active material (e.g., individually or in combination) provided in the fluid stock is about 0.05 wt % or more, e.g., about 0.1 wt % to about 25 wt %, about 0.2 wt % to about 10 wt %, about 0.5 wt % to about 5 wt %, about 1 wt % to about 3 wt %, about 2 wt %, or the like).
  • the fluid stock has any suitable viscosity.
  • fluid stocks utilized in systems and processes herein have a viscosity of about 0.5 centipoise (cP) or more, e.g., about 5 cP or more, or about 1 cP to about 10 Poise. In more specific embodiments, the viscosity is about 10 cP to about 10 Poise.
  • the viscosity of the fluid stocks is independently (i.e., the fluid stock viscosities are the same or different, such as within the parameters provided) at least 200 centipoise (cP), such as at least 500 cP, at least 1000 cP, at least 2000 cP, at least 2,500 cP, at least 3,000 cP, at least 4,000 cP, or the like (e.g., up to 20,000 cP, up to about 10,000 cP, or the like). In preferred embodiments, the viscosity of the fluid stock is about 2,000 cP to about 10,000 cP.
  • relatively small amounts of carbon inclusion are required to form a carbon web, securing the active material of the electrode material and/or electrode.
  • such low carbon loading requirements provide for very high capacities of the overall electrode, not just high capacities of the active material of the electrode.
  • the electrode comprises very high concentrations of active material and, e.g., does not require the use of additional binders (e.g., forming a binder-free electrode), fillers, or the like.
  • additional binders e.g., forming a binder-free electrode
  • such high concentrations of active electrode material in the electrode and/or electrode material provided herein allows for the manufacture of electrodes having the desired capacities while using very little material.
  • processes provided herein are well designed to not only manufacture high capacity materials, but to also manufacture thin electrode materials having very good uniformity and very low defect characteristics (e.g., which defects may result in reduced capacity upon cycling).
  • the carbon inclusion comprises about 20 wt % or less (e.g., about 10 wt % or less, about 5 wt % or less, or about 0.5 wt % to about 3 wt %) of the deposition, or about 20 wt % or less (e.g., about 10 wt % or less, about 5 wt % or less, or about 0.5 wt % to about 3 wt %) of the additives of the fluid stock (i.e., of the non-liquid medium components of the fluid stock).
  • the weight ratio of inclusions is about 8:2 to about 999: 1, e.g., about 85: 15 to about 995:5, about 9: 1 to about 99: 1.
  • the percentage of inclusions (e.g., micro- and/or nano-structures) comprising active material in the electrode or electrode material is about 25 wt % or more, e.g., about 50 wt % or more, about 75 wt % or more, about 80 wt % or more, about 85 wt % or more, about 90 wt % or more, about 95 wt % or more, or the like.
  • the amount of active material in the electrode or electrode material is about 20 wt % or more, e.g., about 40 wt % or more, about 50 wt % or more, about 60 wt % or more, about 70 wt % or more, about 80 wt % or more, about 90 wt % or more, or the like.
  • the liquid medium comprises any suitable solvent or suspending agent.
  • the liquid medium is merely utilized as a vehicle and is ultimately removed, e.g., by evaporation during the electrospraying process and/or upon drying of the deposition.
  • the liquid medium is aqueous.
  • the liquid medium comprises water, alcohol ((e.g., n-, tert-, sec-, or iso-) butanol, (e.g., n-, or iso-) propanol, ethanol, methanol, or combinations thereof), tetrahydrofuran (TUF), dimethylformamide (DMF), N-methyl-2-pyrrolidone ( MP), Dimethylacetamide (DMAc), or combinations thereof.
  • the liquid medium comprises water.
  • any additives in the fluid stock are dissolved and/or well dispersed prior to electrospray, e.g., in order to minimize clogging of the electrospray nozzle (and/or other system components), ensure good uniformity of dispersion of any inclusions in the resulting deposition, and/or the like.
  • the fluid stock is agitated prior to being provided to the nozzle (e.g., inner conduit inlet thereof), or the system is configured to agitate a fluid stock prior to being provided to the nozzle (e.g., by providing a mechanical stirrer or sonication system associated with a fluid stock reservoir, e.g., which is fluidly connected to the inlet of the inner conduit of an electrospray nozzle provided herein).
  • any suitable active electrode material or silicon inclusion material is optionally utilized in electrodes, films, compositions, domains, fluid stocks, aerosols, precursors, or the like described herein.
  • the active electrode material comprises a high energy capacity material (e.g., having a theoretical capacity of greater than graphite, such as > 400 mAh/g, > 500 mAh/g, > 750 mAh/g, > 1,000 mAh/g, or more).
  • the active electrode material is not graphite (non-graphitic).
  • the active electrode material comprises a material having high volume expansion upon lithiation (e.g., > 150%, or > 200%).
  • the active electrode material comprises Si, Ge, Sn, Co, Cu, Fe, any oxidation state thereof, or any combination thereof.
  • the anode or high energy capacity material comprises Si, Ge, Sn, Al, an oxide thereof, a carbide thereof, or an alloy thereof.
  • the anode or high energy capacity material comprises SiOx (e.g., wherein 0 ⁇ x ⁇ 2, or 0 ⁇ x ⁇ 1.5), SiO a N b C c (e.g., wherein 0 ⁇ a ⁇ 2, 0 ⁇ b ⁇ 4/3, and 0 ⁇ c ⁇ 1, and, e.g., wherein a/2 + 3b/4 + c is about 1 or less), Sn, SnOx (e.g., wherein 0 ⁇ x ⁇ 2, or 0 ⁇ x ⁇ 1.5), Si, Al, Ge, or an Si alloy.
  • SiOx e.g., wherein 0 ⁇ x ⁇ 2, or 0 ⁇ x ⁇ 1.5
  • SiOx e.g., wherein 0 ⁇ x ⁇ 2, or 0 ⁇ x ⁇ 1.5
  • SiOx e.g., wherein 0 ⁇ x ⁇ 2, or 0 ⁇ x
  • silicon inclusion materials comprise an active silicon electrode material (e.g., Si, SiOx, or the like) or a precursor thereof.
  • the silicon material comprises a plurality of structures comprising a silicon material.
  • the silicon material is a silicon material that is active in an electrode, such as a negative electrode in a lithium ion battery.
  • the silicon material is, by way of non- limiting example, elemental silicon, and/or a silicon oxide (e.g., having a formula: SiOx, wherein 0 ⁇ x ⁇ 2, e.g., 0 ⁇ x ⁇ 1.5, or 0 ⁇ x ⁇ 1).
  • x is 0 to about 1.5.
  • Any suitable inclusion structure is optionally utilized, such as a fiber, particle, sheet, rod, and/or the like.
  • the silicon-containing inclusion structures are micron or submicron in size, such as nanoscaled structures.
  • silicon-containing inclusions provided herein have an average dimension of less than 100 micron, such as less than 50 micron, or less than 30 micron.
  • the silicon-containing inclusions have an average dimension of less than 25 micron, less than 2 micron, less than 15 micron, less than 10 micron or the like.
  • the silicon-containing inclusions have an average dimension of at least 200 nm, e.g., about 200 nm to about 10 micron.
  • nanostructured inclusions are preferred, such as having an average dimension of about 200 nm or less, such as about 10 nm to about 200 nm.
  • silicon-containing inclusions have a high aspect ratio (length divided by width), such as being in a fiber or rod form, or a low aspect ratio, such as in a spherical form.
  • the silicon- containing inclusions have an average aspect ratio of about 1 to about 100, or more.
  • the silicon-containing inclusions have an average aspect ratio of 1 to about 50, or 1 to about 20, or 1 to about 10.
  • silicon-containing inclusions provided herein have at least one average dimension of less than 100 micron, such as less than 50 micron, or less than 30 micron. In more specific embodiments, the silicon-containing inclusions have an average dimension of less than 25 micron, less than 2 micron, less than 15 micron, less than 10 micron or the like. In certain embodiments, the silicon-containing inclusions have at least one average dimension of at least 200 nm, e.g., about 200 nm to about 10 micron.
  • the silicon-containing inclusions have at least one average dimension of about 200 nm or less, such as about 10 nm to about 200 nm (e.g., a high aspect ratio nanofiber or nanorod, wherein the nanofibers or nanorods have an average diameter of about 10 nm to about 200 nm and a length up to 10 times, up to 100 times, or more the diameter).
  • silicon-containing inclusions utilized herein further comprise an additional material (e.g., as a composite), such as carbon (e.g., amorphous and/or crystalline carbon).
  • Silicon-containing inclusions described herein optionally comprise (e.g., on average) any suitable amount of active electrode silicon material (e.g., Si and/or SiOx), such as about 30 wt. % or more of active electrode silicon material, about 50 wt. % or more of active electrode silicon material, about 70 wt. % or more of active electrode silicon material, or the like.
  • active electrode silicon material e.g., Si and/or SiOx
  • active electrode material containing inclusions or particles used in compositions, films, electrodes, processes, and the like herein comprise silicon and/or a silicon oxide (SiOx, wherein 0 ⁇ x ⁇ 2).
  • the silicon-containing particles comprise a sub-stoichiometric silicon oxide (i.e., SiOx, wherein 0 ⁇ x ⁇ 2).
  • particles described herein as comprising SiOx may comprise both Si and silicon oxide, SiOa (0 ⁇ a ⁇ 2), for an overall x value of 0 ⁇ x ⁇ 2, preferably 0 ⁇ x ⁇ 0.5.
  • inclusions comprising SiOx include reference to the overall x value of an inclusion (e.g., the inclusions may comprise both elemental silicon (Si) and substoichiometic and/or fully oxidized silicon oxide), unless noted otherwise.
  • silicon-containing particles comprise (e.g., on average) about 50 wt % or more silicon (e.g., elemental silicon (Si)).
  • such particles also comprise SiOx (e.g., wherein 0 ⁇ x ⁇ 2).
  • such particles comprise both Si and SiOx (e.g., with SiOx being present on the surface of the particles).
  • silicon-containing particles comprise (e.g., on average) about 0.1 wt % to about 25 wt % (e.g., about 1 wt. % to about 10 wt. %) SiOx.
  • the particles have an average dimension (e.g., overall average dimension) of about 10 nm or more, e.g., about 200 nm or more.
  • the average dimension is about 200 nm (0.2 micron) to about 20 micron, e.g., about 1 to about 10 micron, about 0.5 micron to about 5 micron, or about 1 micron to about 5 micron.
  • the particles have one or more dimension (e.g., length, width, diameter, length, smallest dimension, or the like) having an average size of about 10 nm or more, e.g., about 200 nm or more.
  • the average dimension is about 200 nm (0.2 micron) to about 20 micron, e.g., about 1 to about 10 micron, about 0.5 micron to about 5 micron, or about 1 micron to about 5 micron.
  • particles have an average aspect ratio of 1 or more, such as 1 to about 100, 1 to about 10, or the like.
  • the active electrode material containing (e.g., silicon-containing) particles have an average aspect ratio of 1 to about 100, such as 1 to about 10.
  • active electrode material containing (e.g., silicon-containing) particles have an average dimension (or an average smallest dimension) of about 10 microns or less, e.g., about 200 nm to about 10 micron, or about 1 micron to about 5 micron.
  • the active electrode material (e.g., silicon) containing particles provided herein have high roundness, low sphericity, and/or a small maximum size.
  • the particles have high roundness, low sphericity, and a small maximum size.
  • the particles have other beneficial characteristics, such as low standard deviation in size, and/or the like.
  • control of such characteristics improves control of swelling directionality during lithiation and de-lithiation and/or facilitates better coverage and/or protection of the particles during lithiation and de-lithiation, such as by reducing delamination of the particles during usage (e.g., battery cycling).
  • particles provided herein, as well as particles provided in compositions, electrodes, powders, liquid compositions, aerosols, and the like, and in processes herein are characterized by a number of characteristics.
  • the particles characterized herein have a smallest dimension of less than 100 micron, less than 75 micron, less than 50 micron, less than 40 micron, less than 30 micron, less than 20 micron, less than 10 micron, or the like (e.g., down to about 0.05 micron, about 0.1 micron, about 0.2 micron, or the like).
  • the particles a largest dimension of at least 0.1 micron, at least 0.2 micron, at least 0.3 micron, at least 0.5 micron, at least 1 micron, or the like.
  • compositions and the like provided herein optionally comprise other particles outside of these ranges (particularly at the lower end), but such particles don't necessarily have the characteristics described herein.
  • (e.g., non-precursor) particles provided herein have an average largest dimension of about 20 micron or less, such as about 15 micron or less, about 0.1 micron to about 10 micron, or about 0.2 micron to about 5 micron.
  • fewer than 3% (e.g., fewer than 1%, fewer than 0.5%, fewer than 0.2%, fewer than 0.1%) of the (e.g., non-precursor) particles have a largest dimension of greater than 20 micron. In specific embodiments, fewer than 3% (e.g., fewer than 1%, fewer than 0.5%, fewer than 0.2%, fewer than 0.1%) of the (e.g., non-precursor) particles have a largest dimension of greater than 15 micron.
  • fewer than 3% (e.g., fewer than 1%, fewer than 0.5%, fewer than 0.2%, fewer than 0.1%) of the (e.g., non-precursor) particles have a largest dimension of greater than 10 micron.
  • less than 10 wt. % (e.g., less than 5 wt. %, less than 3 wt. %, less than 1 wt. % or the like) of the particles have a largest dimension of greater than 20 micron.
  • the particles have a largest dimension of greater than 15 micron. In more specific embodiments, less than 10 wt. % (e.g., less than 5 wt. %, less than 3 wt. %, less than 1 wt. % or the like) of the particles have a largest dimension of greater than 10 micron.
  • the particles have an average roundness of about 0.2 or more. In specific embodiments, the particles have an average roundness of about 0.3 or more. In more specific embodiments, the particles have an average roundness of about 0.4 or more. In still more specific embodiments, the particles have an average roundness of about 0.5 or more. In yet more specific embodiments, the particles have an average roundness of about 0.6 or more. Roundness is determined by a suitable measure available in the art, such as either one of the following:
  • N total number of corners
  • the particles have an average sphericity of about 0.8 or less. In specific embodiments, the particles have an average sphericity of about 0.7 or less. In more specific embodiments, the particles have an average sphericity of about 0.6 or less. In still more specific embodiments, the particles have an average sphericity of about 0.5 or less. In yet more specific embodiments, the particles have an average sphericity of about 0.4 or less. In certain embodiments, the particles have an average aspect ratio of at least 1.1, of at least 1.2, of at least 1.3, of at least 1.5, of at least 2, or the like. Sphericity is determined by a suitable measure available in the art, such as either one of the following:
  • the particles have a standard deviation of the largest dimension thereof equal to about twice average largest dimension thereof or less (or, the coefficient of variance (CV), being the standard deviation (SD) / average, is equal to or less than about 2).
  • the coefficient of variance is ⁇ 1.5, ⁇ 1.2, ⁇ 1, ⁇ 0.9, ⁇ 0.8, or the like.
  • fewer than 50%, fewer than 40%, fewer than 30%, fewer than 20%, fewer than 10%) or the like are caked (e.g., by number or by weight).
  • caking of the particles occurs when aggregated domains form within a particle composition, such as wherein aggregated domains have a size of greater than 50 micron, greater than 40 micron, greater than 30 micron, greater than 20 micron, or the like (e.g., wherein the aggregate flows, such as with a bulk solid or powder of which it is a part, but the particles comprising the aggregate do not independently flow).
  • an inclusion (e.g., in the fluid stock, droplets, and/or electrode or deposition) comprises a composite of an active electrode material.
  • the inclusion further comprises a second material (e.g., carbon, ceramic, or the like).
  • the inclusions are nanoscale inclusions, such as nanofibers, nanorods, or nanoparticles.
  • the inclusion is a composite (e.g., nanofiber) comprising carbon and a silicon material (e.g., having the formula SiOx, wherein 0 ⁇ x ⁇ 2, or other active silicon material, such as described herein).
  • such materials are optionally manufactured according to any suitable technique, with exemplary techniques being described in US Patent Application No. 14/382,423, entitled “Silicon Nanocomposite Nanofibers," US Patent Application No. 14/457,994, entitled “Carbon and Carbon Precursors in Nanofibers,” and US Patent Application No. 62/111,908, entitled “Silicon-Carbon Nanostructured Composites,” all of which are incorporated herein for the disclosure of such materials and methods of manufacturing such materials.
  • nanostructures comprising electrode active material provided herein are manufactured by dispersing silicon nanoparticles (i.e., nanoparticles comprising silicon, and, in some instances, oxides thereof) in a fluid stock (e.g., with a polymer and liquid medium), electrospinning (e.g., gas-assisted electrospinning) the fluid stock, carbonizing the product (e.g., nanofibers) thereof.
  • the inclusion is a carbon nanostructure (e.g., a carbon nanotube or a hollow carbon nanofiber) infused with a silicon material described herein (e.g., silicon or an SiOx material described herein).
  • FIG. 10 illustrates the capacity retention
  • FIG. 11 illustrates the cycling efficiencies of half cells prepared using exemplary silicon-carbon composite fiber materials as the active electrode containing inclusion material in the anode materials described herein.
  • the carbon material is any suitable carbon material, such as a nanostructured carbon material.
  • the carbon material is a carbon sheet, a carbon ribbon, or the like.
  • the carbonaceous inclusions are grapheme components (e.g., graphene, graphene oxide, reduced graphene oxide, sheets thereof, ribbons thereof, or the like), carbon nanotubes (e.g., multi-walled carbon nanotubes (MWCNTs)), graphite, other carbon allotropes, or oxides, analogs or derivatives thereof, such as described herein.
  • the carbon inclusion material is a graphene component, e.g., graphene or an analog there, such as graphene that has one or more carbon atom thereof substituted with one or more additional atom, such as oxygen, halide, hydrogen, and/or the like.
  • graphene or graphenic components herein have a general two- dimensional structure (e.g., with 1 -25 layers), with a honey-comb lattice structure (which in some instances, such as in non-pristine graphene, graphene oxide, reduced graphene oxide, or the like, may comprise certain defects therein, such as described and illustrated herein).
  • the graphene component is an oxidized graphene component.
  • the carbon material is or comprises a graphene component, such as graphene, graphene oxide, reduced graphene oxide, or a combination thereof.
  • the oxidized graphene component comprises about 60% or more carbon (e.g., 60% to 99%).
  • the oxidized graphene component comprises about 60 wt. % to about 90 wt. % carbon, or about 60 wt. % to about 80 wt. % carbon.
  • the oxidized graphene component comprises about 40 wt. % oxygen or less, such as about 10 wt.
  • the oxidized graphene component comprises sufficient oxygen so as to facilitate dispersion and opening of the graphene sheets in an aqueous medium.
  • the total percentage of carbon and oxygen does not constitute 100% of the graphene component or analog, with the additional mass comprising any suitable atoms, such as hydrogen (and/or, e.g., nitrogen (e.g., in the form of amine, alkyl amine, and/or the like).
  • graphene components utilized in the processes and materials utilized herein optionally comprise pristine graphene sheets, or defective graphene sheets, such as wherein one or more internal and/or external rings are oxidized and/or opened, etc.
  • a graphene oxide is utilized in the fluid stock and, following electrospraying of the fluid stock, the collected deposition is thermally treated (e.g., to a temperature of about 100 °C or more, e.g., 150 °C to 400 °C, about 150 °C to about 350 °C, about 200 °C to about 300 °C, about 200 °C, about 250 °C, or any suitable temperature), such as to at least partially reduce the graphene oxide (i.e., decrease the percentage of oxygen relative to carbon in the graphene oxide).
  • any other suitable technique is optionally utilized to reduce the graphene oxide following deposition.
  • reduction of the graphene oxide following deposition improve the performance characteristics of the material (e.g., by, in some instances, increasing conductivity of the carbon inclusion).
  • various figures provided herein illustrate that in some instances, materials provided herein demonstrate improved performance (e.g., specific capacity) characteristics with reduced graphene oxide (rGO), relative to graphene oxide (GO).
  • rGO reduced graphene oxide
  • GO graphene oxide
  • a carbon inclusion utilized in fluid stocks and materials herein has any suitable dimension.
  • the carbon inclusion is a two dimensional material, such as a graphene component (e.g., graphene oxide, reduced graphene oxide, graphene, or the like).
  • the two dimensional material e.g., graphene component
  • has a first dimension and a second dimension e.g., length and width
  • active material inclusions have three dimensions (e.g., length, width, height for particles, or diameter and length for rods/fibers) having an average dimension.
  • carbon inclusions utilized are of a size sufficient to coat or wrap, such as in an envelope or web, the active material inclusions upon electrospray deposition.
  • the average dimension of a (e.g., two dimensional) carbon inclusion is equal to or greater than the average dimension of the active material inclusions.
  • larger carbon inclusions provide the ability to wrap or envelop multiple active material inclusions.
  • the average dimension of the carbon inclusion is about O. lx to about 500x the average dimension of the active material inclusion.
  • the average dimension of the carbon inclusion is about lx to about 200x the average dimension of the active material inclusion.
  • the dimension of the carbon inclusion is about 5x to about 25x, such as about lOx, the average dimension of the active material inclusion (e.g., wherein the electrode active material inclusions have an average dimension of about 200 nm or more). In other specific embodiments, the dimension of the carbon inclusion is about 50x to about 250x, such as about lOOx, the average dimension of the active material inclusion (e.g., wherein the electrode active material inclusions have an average dimension of about 200 nm or less). In some embodiments, the average dimension of a two- dimensional carbon inclusion is about 1 micron to about 20 micron (e.g., about 5 micron to about 10 micron).
  • carbon inclusions e.g., two-dimensional carbon inclusions, such as graphene components
  • carbon inclusions e.g., two-dimensional carbon inclusions, such as graphene components
  • have at least one average dimension e.g., lateral dimension (longest side length), width and/or length) (that is, the measure of the dimension, on average, within the carbon inclusions of the processes or compositions provided herein) that is at least equal to the average dimension (or the average smallest dimension - particularly in instances where higher aspect ratio (e.g., >2, >5, >10, or the like) active electrode material containing particles are utilized) of the active electrode material containing (e.g., silicon-containing) particles.
  • the average dimension e.g., lateral dimension (longest side length), width and/or length
  • the average dimension e.g., the average smallest dimension - particularly in instances where higher aspect ratio (e.g., >2, >5, >10, or the like) active electrode material containing particles are utilized) of the active electrode material
  • carbon inclusions provided herein have at least one average dimension that is >lx (e.g., > l . lx, >1.2x, >1.5x, >2x, >3x, >4x, or the like) the average dimension (or the average of the smallest dimension) of the active electrode material containing particles.
  • carbon inclusions (e.g., graphene components) provided herein have at least one average dimension (e.g., width and/or length) that is at least five times (e.g., about 2 times to about 20 times, about 10 times, or about 100 times) the average dimension (or the average smallest dimension) of the active electrode material containing (e.g., silicon-containing) particles.
  • the carbon inclusions e.g., graphene components
  • the thickness of the carbon inclusion is about 1 nm or about 1 nm to about 10 nm, or about 3-5 nm.
  • a carbon inclusion or graphene components described herein comprises one or more layers (e.g., graphene component layers) thereof (e.g., each graphene layer comprising a graphene, graphene oxide, reduced graphene oxide, or the like).
  • a graphene component provided herein comprises an average of about 1 to about 25 layers thereof.
  • graphene envelopes described herein comprising such carbon inclusions or graphene components comprise such thicknesses and/or number of layers therein.
  • the carbon inclusion e.g., two-dimensional carbon inclusions, such as graphene components
  • has an average dimension e.g., lateral dimension, width and/or length of about 0.5 micron or more, about 1 micron or more, about 5 micron or more, about 1 micron to about 100 micron, about 5 micron to about 50 micron, or the like.
  • compositions e.g., base compositions or domains
  • webs, envelopes, films, or the like e.g., of compositions provided herein
  • carbon inclusions e.g., graphene component or oxidized graphene component
  • particles e.g., electrode active material, such as silicon
  • the carbon inclusion is an oxidized graphene component and the weight ratio of particles (e.g., comprising silicon) to oxidized graphene component (e.g., graphene oxide) is about 1 :5 to about 5: 1, e.g., about 1 : 1 to about 5: 1, or about 1 : 1 to about 3 : 1.
  • ratio of particles (e.g., comprising silicon) to oxidized graphene component (e.g., graphene oxide) is about 3 :2 to about 5: 1.
  • compositions provided herein comprise 20 wt. % or more, about 30 wt. % or more, about 40 wt. % or more, about 50 wt.
  • pre-thermally treated compositions or films have lower wt. % that post-thermally treated compositions (e.g., because upon thermal treatment, the carbonaceous inclusion, such as graphene oxide, is reduced, losing oxygen and molecular weight and mass).
  • pre-thermally treated compositions comprise about 30 wt. % to about 80 wt. % active electrode material (e.g., SiOx).
  • post-thermally treated compositions comprise about 50 wt. % to about 95 wt. % electrode active material (e.g., SiOx).
  • electrode active material e.g., SiOx
  • compositions provided herein comprise 5 wt. % or more, about 10 wt. % or more, about 30 wt. % or more, or the like of carbon inclusion materials (e.g., grapheme component).
  • up to about 80 wt %, up to about 70 wt. %, up to about 50 wt. %, up to about 30 wt. % or the like of carbon inclusion materials (e.g., grapheme component) is optionally included.
  • pre-thermally treated compositions comprise about 20 wt. % to about 80 wt. % carbon inclusion materials (e.g., grapheme component).
  • post-thermally treated compositions comprise about 10 wt. % to about 50 wt. % carbon inclusion materials (e.g., grapheme component).
  • a composition or film provided herein comprises a plurality of active electrode material containing (e.g., silicon-containing) particles and a plurality of carbon inclusions (e.g., oxidized graphene components).
  • a (e.g., pre- and/or post-thermally treated) composition or film provided herein comprises active electrode material containing particles secured within a carbonaceous web (e.g., grapheme web).
  • the web defines one or more pockets (e.g., grapheme pockets) within which one or more of the active electrode material containing particles are configured.
  • the composition or film comprises a plurality of graphene envelopes, the graphene envelopes comprising an external surface and an internal surface, the internal surface defining a graphene pocket.
  • one or more of the active electrode material containing (e.g., silicon-containing) particles are configured within the graphene pocket.
  • the graphene envelopes comprise one or more of the carbon inclusions of a (e.g., first or base) composition or layer (e.g., oxidized graphene component(s)).
  • a graphene pocket(s) comprise at least 1 active electrode containing particle configured therewithin (e.g., on average).
  • a graphene pocket comprises, on average, greater than 1 (e.g., at least 1.05) active electrode containing particles configured therewithin.
  • a graphene pocket(s) comprise 1 to 200 or 1 to 100 active electrode material containing (e.g., silicon-containing) particles configured therewithin (e.g., 1 ⁇ n ⁇ 100, 1.01 ⁇ n ⁇ 200, 1.05 ⁇ n ⁇ 100, or the like wherein n is the number of active electrode containing particles configured within the envelope) (e.g., on average).
  • the graphene pocket(s) comprise 1-50 (e.g., 1-5, or 2-5) (e.g., 1 ⁇ n ⁇ 50, l ⁇ n ⁇ 5, 2 ⁇ n ⁇ 5) active electrode material containing (e.g., silicon- containing) particles configured therewithin (e.g., on average).
  • a (e.g., thermally) treated composition or film comprises a plurality of active electrode material containing (e.g., silicon-containing) particles and a plurality of carbon inclusions (e.g., oxidized graphene components that have been (e.g., thermally) reduced).
  • a composition or film e.g., pre- and/or post-thermally treated composition or film
  • the web defines one or more pockets (e.g., grapheme pockets) within which one or more of the active electrode material containing particles are configured.
  • the (e.g., thermally) treated composition or film comprises a plurality of graphene envelopes, the graphene envelopes comprising an external surface and an internal surface, the internal surface defining a graphene pocket.
  • one or more of the active electrode material containing (e.g., silicon-containing) particles are configured within the graphene pocket.
  • the graphene envelopes or pocket walls comprise one or more of the carbon inclusions of the treated composition or film (e.g., oxidized graphene component(s) that have been (e.g., thermally) reduced).
  • a graphene pocket(s) comprise 1-100 active electrode material containing (e.g., silicon-containing) particles configured therewithin (e.g., on average).
  • the graphene pocket(s) comprise 1-50 (e.g., 1-5, or 2-5) active electrode material containing (e.g., silicon-containing) particles configured therewithin (e.g., on average).
  • pockets described herein have a volume that is greater than the volume of the particle(s) configured therewithin. In certain instances, pocket volume excess is desirable, particularly when the active electrode material expands during lithiation, such as Si and/or SiOx.
  • the excess volume allows the particles to expand while reducing the opportunity for the web coating to become displace and/or while reducing the overall volume expansion of the electrode material.
  • the void space within the pocket is at least 3% greater (e.g., at least 5% greater, at least 10% greater, at least 20% greater, or the like) than the volume of the active electrode containing particle(s) configured therewithin.
  • a composition (e.g., pre- and/or post-thermally treated composition) provided herein comprises active electrode material containing particles secured within a carbonaceous web (e.g., grapheme web).
  • the web defines one or more pockets (e.g., grapheme pockets) within which one or more of the active electrode material containing particles are configured.
  • a grapheme web is a collection of a plurality of grapheme component sheets (e.g., graphene sheets, graphene oxide sheets, reduced graphene oxide sheets, or combinations thereof) that collectively form a layer having a surface area larger than the surface area of a single sheet.
  • the grapheme components overlap, adjoin, abut, or otherwise interact or interface with one another (e.g., through non- covalent forces).
  • the carbonaceous (e.g., grapheme) film comprises a continuous web defining a large number of carbonaceous pockets therein.
  • the continuous web extends throughout the composition, providing a continuous, self-supporting film.
  • a carbonaceous web forms a coating or wrap around one or more active electrode material containing particles in a single graphenic pocket, such as without having interconnectivity with a second graphenic pocket structure.
  • FIG. 5 and FIG. 9 illustrates graphenic webs having a high degree of interconnectivity between graphenic pockets.
  • a film or composition provided herein has an externally exposed surface (e.g., including the top surface and other exposed surfaces of the materials exemplified in the figures herein), the externally exposed surface being comprised primarily of carbonaceous material.
  • the electrode active material e.g., SiOx
  • the electrode active material has very little external exposure in the film or composition, even more limited than in cases where a top coat is not present, such as described herein. In some instances, this is important to maximizing electrode performance characteristics, such as by minimizing pulverization and/or SEI formation.
  • compositions, films, or (coated) particles provided herein comprise less than 3 % electrode active material or SiOx by surface area. In more preferred embodiments, compositions, films, or (coated) particles provided herein comprise less than 1 % electrode active material or SiOx by surface area. In some embodiments, compositions, films, or (coated) particles provided herein is at least 90 % graphenic (e.g., characterized by a graphene component described herein) by surface area. In preferred embodiments, compositions, films, or (coated) particles provided herein is at least 95 % grapheme by surface area. In more preferred embodiments, compositions, films, or (coated) particles provided herein is at least 98 % (e.g., at least 99%) grapheme by surface area.
  • a composition or film e.g., comprising a base and top coat
  • a plurality of active electrode material e.g., silicon
  • carbon inclusions e.g., graphene components, oxidized graphene components, oxidized graphene components that have been reduced, or the like.
  • the carbon inclusions are oxidized graphene components.
  • the carbon inclusions are graphene components (e.g., oxidized graphene components that have been reduced).
  • the compositions comprise a plurality of silicon-carbon composite domains.
  • silicon-carbon composite domains comprise an (e.g., graphene) envelope, the envelope comprising an external surface and an internal surface, the internal surface defining an envelope pocket.
  • one or more of the plurality of active electrode material (e.g., silicon) containing particles are configured within the envelope pocket.
  • the envelope comprises one or more of the plurality of carbon inclusions (e.g., graphene components, oxidized graphene components, or the like).
  • composition comprising graphene oxide and a plurality of silicon-containing particles, the graphene oxide configured to form a plurality of graphene oxide envelopes, the plurality of silicon-containing particles being configured within the plurality of graphene oxide envelopes.
  • composition comprising reduced graphene oxide and a plurality of silicon-containing particles, the reduced graphene oxide configured to form a plurality of reduced graphene oxide envelopes, the plurality of silicon-containing particles being configured within the plurality of reduced graphene oxide envelopes.
  • envelopes e.g., graphene envelopes
  • a plurality of particles e.g., comprising electrode active material, such as silicon
  • a (e.g., micro- or nano-structured) silicon material is dispersed in and/or on a carbon (e.g., graphene) matrix, web (e.g., wherein the graphene matrix or web comprises a graphene structure or analog as described herein), pockets, and/or envelopes.
  • the carbon web e.g., comprising envelopes thereof
  • the carbon web is about 25 wt. % or more (e.g., about 50 wt % or more, about 60 wt % or more, about 75 wt % or more, about 85 wt % or more, about 90 wt % or more, or about 95 wt % or more) graphene component.
  • the silicon material comprises a plurality of nanostructures (e.g., such nanostructures comprising a nanoscale (e.g., having an average dimension of less than 2 micron, or less than 1 micron) structure in any one or more dimension, such as nanostructured fibers, particles, sheets, rods, and/or the like) comprising a silicon material.
  • the silicon material comprises a plurality of larger structures, such as microstructures (e.g., having an average dimension of less than 100 micron, less than 50 micron, or less than 30 micron, preferably less than 25 micron, less than 20 micron, less than 15 micron, less than 10 micron, or the like, such as down to about 200 nm).
  • Suitable electrode active materials and/or silicon-containing or based materials, inclusions, or structures are as described herein. Further, in some instances, such as wherein larger structures are utilized, larger droplets or particles are necessarily formed upon electrospray according to the processes described herein.
  • silicon materials included herein include a silicon material that is active in an electrode, such as a negative electrode in a lithium ion battery, such as elemental silicon, and/or a silicon oxide (e.g., having a formula: SiOx, wherein 0 ⁇ x ⁇ 2, e.g., 0 ⁇ x ⁇ 1.5, 0 ⁇ x ⁇ 1, or x ⁇ 0).
  • silicon materials and/or inclusions included in the compositions, materials, and electrodes described herein comprise silicon (elemental silicon), such as crystalline silicon.
  • silicon-containing particles provided herein comprise 40 wt.
  • silicon-containing particles provided herein comprise 50 wt. % (e.g., 60 wt % or more, 70 wt. % or more, 80 wt % or more, or the like) or more electrode active silicon material (e.g., SiOx). In some embodiments, silicon-containing particles provided herein comprise 40 wt. % or more electrode active silicon (Si). In specific embodiments, silicon- containing particles provided herein comprise 50 wt. % (e.g., 60 wt % or more, 70 wt. % or more, about 70 wt.
  • Si silicon
  • SiOx SiOx
  • compositions comprising a plurality of active electrode inclusions (e.g., silicon-containing particles) and a plurality of carbon inclusions (e.g., graphene components, such as a reduced graphene oxide component, such as rGO).
  • the carbon inclusions e.g., graphene components
  • each envelope comprises one or more (e.g., at least 2) carbon inclusions (e.g., graphene components, such as a reduced graphene oxide component, such as rGO).
  • each envelope comprises an internal surface and an external surface, the internal surface defining an envelope pocket.
  • individual carbon inclusions optionally form all or part of one or more envelope, such as illustrated in FIG. 4.
  • the external surface of one envelope forms all or part of the internal surface of a second envelope.
  • the web and/or envelopes taken together with active electrode materials comprise a plurality of composite domains within the composition or material.
  • composite domains comprise an envelope and active material (e.g., inclusions, such as particles thereof).
  • compositions or material comprising a graphene component, such as an oxidized graphene component (e.g., graphene oxide).
  • a composition or material herein comprises a plurality of graphene envelopes, the graphene envelopes comprising one or more oxidized graphene components (e.g., graphene oxide).
  • such compositions or materials are precursor materials to electrode materials described herein.
  • such precursor materials are converted to electrode materials via reductive reaction conditions, such as through thermal, chemical, or other processes described herein.
  • the oxidized graphene component is a graphene component functionalized with oxygen, such as with carbonyl groups, carboxyl groups (e.g., carboxylic acid groups, carboxylate groups, COOR groups, such as wherein R is a C1-C6 alkyl, or the like), -OH groups, epoxide groups, and/or the like.
  • the oxidized graphene component (or graphene oxide) comprises about 60% or more carbon (e.g., 60% to 99%).
  • the oxidized graphene component comprises about 60 wt. % to about 90 wt. % carbon, or about 60 wt. % to about 80 wt. % carbon.
  • the oxidized graphene component comprises about 40 wt. % oxygen or less, such as about 10 wt. % oxygen to about 40 wt. % oxygen, about 35 wt. % oxygen or less, about 1 wt. % to 35 wt. % oxygen, or the like.
  • the weight ratio of active electrode material or silicon-containing particles to carbon inclusion of compositions, films, or materials is about 1 : 10 to about 20: 1.
  • Other ratios, such as those described herein are also contemplated. In various instances, such ratios include ratios of the active electrode material containing domain, composition or coat, or of the entire film (e.g., both base and top coats).
  • compositions or material comprising a graphene component, such as an oxidized graphene component that has been reduced (e.g., reduced graphene oxide).
  • a composition or material herein comprises a plurality of graphene envelopes, the graphene envelopes comprising one or more (oxidized or reduced oxidized) graphene components (e.g., reduced graphene oxide).
  • such compositions or materials are electrode materials prepared from precursor materials described herein.
  • such electrode materials are converted from precursor materials via reductive reaction conditions, such as through thermal, chemical, or other processes described herein.
  • the (e.g., reduced oxidized) graphene component is a graphene component functionalized with oxygen, such as with carbonyl groups, carboxyl groups (e.g., carboxylic acid groups, carboxylate groups, COOR groups, such as wherein R is a C1-C6 alkyl, or the like), -OH groups, epoxide groups, and/or the like.
  • oxygen such as with carbonyl groups, carboxyl groups (e.g., carboxylic acid groups, carboxylate groups, COOR groups, such as wherein R is a C1-C6 alkyl, or the like), -OH groups, epoxide groups, and/or the like.
  • oxidized graphene components generally comprise less oxidation that oxidized graphene components, residual oxidation and defects remain present in some instances.
  • the graphene component e.g., reduced graphene oxide
  • the graphene component (e.g., rGO) comprises about 35 wt. % or less (e.g., 0.1 wt. % to 35 wt. %) oxygen, e.g., about 25 wt. % or less (e.g., 0.1 wt. % to 25 wt. %) oxygen, or about, about 20 wt.
  • the graphene component (e.g., rGO) comprises about 0.1 wt. % to about 10 wt. % oxygen, e.g., about 4 wt. % to about 9 wt. %, about 5 wt, % to about 8 wt, %, or the like.
  • the weight ratio of active electrode material or silicon-containing particles to carbon inclusion of compositions or materials is about 1 :5 to about 20: 1.
  • envelopes of compositions, materials, and electrodes described herein comprise any suitable number of active material inclusions (or precursors thereof) in the pockets thereof.
  • individual envelopes comprise one or more inclusions therein.
  • individual envelopes comprise 2 or more (e.g., 2-10, 2-5, or the like) inclusions therein.
  • inclusions e.g., micro- structured inclusions, such as having a particle size (or average dimension) of greater than about 200 nm on average, about 1 micron to about 10 micron, or the like are utilized
  • fewer inclusions are found within the envelope pockets, such as about 1 to about 10, or about 2 to about 5 inclusions on average, or 1 to 10, e.g., 2 to 5, in individual envelopes.
  • inclusions e.g., nano-structured inclusions, such as having one or more, or an average dimension, of less than 200 nm
  • more inclusions may be found within the envelope pockets, such as about 1 to about 1000 on average (e.g., about 50 to about 200, such as about 100), or 1 to 1000 (e.g., 50 to 20, such as about 100) in individual envelopes.
  • articles of manufacture comprising a silicon/carbon deposition described herein, e.g., a thin-layered deposition, manufactured or capable of being manufactured according to the processes described herein.
  • a substrate such as a conductive substrate (e.g., current collector), comprising an electrode or deposition described herein on the surface thereof.
  • devices such as energy storage devices, including, e.g., batteries, such as lithium ion batteries, comprising such materials described herein.
  • an electrode or, e.g., a lithium ion battery comprising such an electrode
  • a carbon web securing a plurality of nanostructured inclusions
  • the nanostructured inclusions comprising an electrode active material (e.g., a negative electrode active material, such as a silicon material described herein).
  • FIG. 1 illustrates an electrode deposition 101 on a current collector 104.
  • the electrode may comprise carbon web 102 securing a plurality of electrode active nanostructures 103.
  • FIG. 1 illustrates an electrode deposition 101 on a current collector 104.
  • the electrode may comprise carbon web 102 securing a plurality of electrode active nanostructures 103.
  • the carbon material 102 such as carbon sheets or ribbons (e.g., graphene, graphene oxide (GO), reduced graphene oxide (rGO), or other graphene analogs), wrap and secure the electrode active nanostructures 103.
  • the carbon material 102 securing the electrode active material 103 functions to protect the electrode active material 103 from interactions with electrolyte, from pulverization, and/or the like.
  • the carbon material 102 facilitates electron conductivity in the electrode.
  • the active electrode material is included in the form of or as a part of a particulate inclusion (e.g., nanoscaled - such as less than about 2 micron in at least one dimension - particulate (e.g., nanoparticles being less than about 2 micron in all dimensions, and nanorods and nanofibers being less than about 2 micron in diameter and greater or less than about 2 micron in a second dimension); or other small structured particle, such as having an average dimension as described herein, such as less than 30 micron, less than 20 micron, less than 15 micron, or the like (e.g., particles, rods or other structure configuration).
  • a particulate inclusion e.g., nanoscaled - such as less than about 2 micron in at least one dimension - particulate (e.g., nanoparticles being less than about 2 micron in all dimensions, and nanorods and nanofibers being less than about 2 micron in diameter and greater or less than about 2 micron in a second dimension)
  • nano-inclusions e.g., nanoparticles
  • nanoscale morphologies that are about 1 micron or less, about 500 nm or less, about 250 nm or less, or about 100 nm or less.
  • at least one dimension e.g., all dimensions for a nanoparticle
  • the particulate inclusion is in the form of a high aspect ratio structures, such as a nanorod or nanofiber.
  • the high aspect structures have a first dimension that is about 2 microns or less, such as about 1 micron or less, about 0.5 micron or less, or about 0.1 micron to about 0.2 micron.
  • such high aspect ratio structures have an aspect ratio of about 10 or more, about 20 or more, about 25 or more, or about 50 or more, such as up to about 250.
  • the second dimension of the high aspect ratio structures is about 50 micron or less, such as about 1 micron to about 50 micron, about 2 micron to about 25 micron, or the like.
  • microscaled particles comprising active material (e.g., SiOx) in (a) pristine form, as well as (b) and (c) covered by carbon (e.g., graphene oxide) (at various zoom levels).
  • active material e.g., SiOx
  • carbon e.g., graphene oxide
  • FIG. 9 illustrates microscaled particles comprising active material (e.g., SiOx) in (a) pristine form, as well as (b) and (c) covered by carbon (e.g., graphene oxide) (at various zoom levels).
  • active material e.g., SiOx
  • carbon e.g., graphene oxide
  • electrodes and/or electrode materials (e.g., films) provided herein have a first cycle Coulombic efficiency of about 80% or more, more preferably about 85% or more. In more preferred embodiments, the electrodes and/or electrode materials (e.g., films) provided herein have a first cycle Coulombic efficiency of about 88% or more, more preferably about 90% or more.
  • a thin layer electrode e.g., comprising an electrode material provided herein
  • a current collector e.g., in two parts.
  • the electrode is well adhered to the current collector.
  • the electrode is adheres to the current collector such that after at least two times (e.g., at least three times, at least five times, or the like) folding the electrode/current collector at an angle of at least 90 degrees (e.g., at least 135 degrees), there is less than 10 % (e.g., less than 5%, less than 3%, less than 1%, or the like) exfoliation of the electrode (e.g., wherein the exfoliation is the % separation of the electrode from the current collector, e.g., by area).
  • the electrode is a thin layer electrode (e.g., deposited on a current collector).
  • the electrode has a thickness of about 500 microns or less, e.g., about 250 microns or less, about 200 microns or less, about 25 microns to about 500 microns, about 50 microns to about 200 microns, or the like.
  • the electrode has a mass loading on a substrate of about 10 mg/cm 2 or less, such as about 0.1 mg/cm 2 to about 10 mg/cm 2 , about 5 mg/cm 2 or less, about 4 mg/cm 2 or less, about 3 mg/cm 2 or less, about 1 mg/cm 2 to about 2 mg/cm 2 .
  • high areal density materials are utilized, such as about 0.1 mg/cm 2 or more, about 0.5 mg/cm 2 or more, or about mg/cm 2 or more (such as about 0.5 mg/cm 2 to about 5 mg/cm 2 , e.g., about 1 mg/cm 2 to about 5 mg/cm 2 ).
  • electrodes and/or materials provided herein have good capacity by area of electrode.
  • electrodes and materials provided herein have an areal capacity of at least 1 mAh/cm 2 , such as about 2 mAh/cm 2 or more, about 3 mAh/cm 2 or more, or about 2 mAh/cm 2 to about 5 mAh/cm 2 .
  • FIG. 12 illustrates capacities and capacity retention of exemplary full cells having an anode with a capacity of about 3 mAh/cm 2 , up to about 2 times greater than exhibited in conventional lithium ion battery full cells.
  • the current collector is any suitable material, such as a metal (e.g., aluminum, copper, or the like) (such as a metal foil) or a carbon substrate (e.g., carbon cloth, carbon paper, or the like).
  • a carbon substrate provides improved flexibility to the combined electrode and current collector product.
  • electrode materials and electrodes provided herein have high capacities (e.g., specific capacities in a lithium ion cell, such as a half cell or full cell).
  • the electrode or electrode material has a specific capacity (e.g., in a half cell) of at least 1,500 mAh/g, at least 1,750 mAh/g, at least 2,000 mAh/g, at least 2,200 mAh/G, or the like at a charge rate of at least C/3 (e.g., C/2) (e.g., wherein C is the rate required to charge/discharge a battery in 1 hour).
  • the electrode material and/or electrode has a specific capacity of about 500 mAh/g or more at a charge rate of about 1 A/g. In more specific embodiments, the electrode material and/or electrode has a specific capacity of about 600 mAh/g or more at a charge rate of about 1 A/g. In still more specific embodiments, the electrode material and/or electrode has a specific capacity of about 700 mAh/g or more at a charge rate of about 1 A/g. In yet more specific embodiments, the electrode material and/or electrode has a specific capacity of about 800 mAh/g or more at a charge rate of about 1 A/g.
  • the electrode material and/or electrode has a specific capacity of about 1000 mAh/g or more (e.g., about 1100 mAh/g or more, or about 1200 mAh/g or more) at a charge rate of about 1 A/g. In some embodiments, the electrode material and/or electrode has a specific capacity of about 500 mAh/g or more at a charge rate of about 2 A/g. In more specific embodiments, the electrode material and/or electrode has a specific capacity of about 600 mAh/g or more at a charge rate of about 2 A/g. In still more specific embodiments, the electrode material and/or electrode has a specific capacity of about 700 mAh/g or more at a charge rate of about 2 A/g.
  • the electrode material and/or electrode has a specific capacity of about 800 mAh/g or more at a charge rate of about 2 A/g. In more specific embodiments, the electrode material and/or electrode has a specific capacity of about 1000 mAh/g or more (e.g., about 1100 mAh/g or more, or about 1200 mAh/g or more) at a charge rate of about 2 A/g.
  • such capacities are observed on the initial cycle (charge and/or discharge cycle), on or after the 2 nd cycle, on or after the 5 th cycle, on or after the 10 th cycle, on or after the 50 th cycle, on or after the 100 th cycle, on or after the 150 th cycle, on or after the 200 th cycle, on or after the 250 th cycle, or a combination thereof.
  • the specific capacity of the electrode material and/or electrode on or after the 200 th and/or 250 th cycle is about 80% or more (e.g., 85% or more) of the specific capacity of the electrode material and/or electrode on the 1 st cycle, the 5 th cycle, and/or the 10 th cycle.
  • a battery e.g., a lithium battery, such as a lithium ion battery
  • a battery provided herein comprises a positive electrode and a negative electrode, at least one electrode thereof being an electrode described herein
  • a battery comprising a negative electrode comprising a direct deposit electrode described herein, an electrode material described herein, and/or a carbon-silicon web and/or envelope described herein.
  • a lithium ion battery comprising a negative electrode, a positive electrode, a separator, and an electrolyte, the negative electrode comprising an electrode described herein (e.g., a carbon web securing a plurality of nanostructured inclusions therein, the nanostructured inclusions comprising an active (electrode) material).
  • an electrode described herein e.g., a carbon web securing a plurality of nanostructured inclusions therein, the nanostructured inclusions comprising an active (electrode) material.
  • binder-free electrodes such as made possible by the manufacturing processes described herein.
  • Provided in some embodiments herein is a general method of manufacturing such electrodes using any suitable materials.
  • provided herein is a general approach to manufacturing very uniform electrodes, in a very efficient manner.
  • processes described herein provide for the direct deposition of electrode on a conductive substrate (e.g., current collector) without the need for downstream processing, such as drop casting, slurry casting, undergoing long or high temperature drying steps, and/or the like.
  • a film provided herein has a first domain and a second domain, such as a base coat and a top coat.
  • the first domain or base coat comprises an active electrode material inclusion and a carbon inclusion, such as described herein and in the morphologies described herein (e.g., wherein the active electrode material (e.g., silicon containing) inclusions reside within grapheme pockets, etc.).
  • the active electrode material inclusions are SiOx inclusions and the carbon inclusions are grapheme components.
  • the grapheme component is graphene oxide (e.g., wherein the film is an anode or anode material precursor), or reduced graphene oxide (e.g., wherein the film is an anode or anode material).
  • the top coat is free or substantially free from non-graphitic, non-graphenic, high capacity, and/or silicon- containing active electrode materials.
  • the top coat comprises less than 10 wt. % high capacity or silicon-containing active electrode materials or inclusion particles.
  • the top coat comprises less than 5 wt. %, less than 3 wt. %, less than 2 wt. %, or less than 1 wt. % high capacity or silicon-containing active electrode materials or inclusion particles.
  • the top coat is a continuous structure, or a non-continuous film. In certain instances, the top coat is so thin that the coverage is insufficient to form a continuous film.
  • a base (active electrode or silicon containing) coat has a base coat average thickness
  • the top coat has a top coat average thickness, with the ratio of the base coat average thickness to the top coat average thickness being at least 1 : 1.
  • the ratio of the base average thickness to the top coat average thickness is at least 2: 1.
  • the ratio of the base coat average thickness to the top coat average thickness is at least 5: 1 (e.g., at least 10: 1).
  • the first composition is highly loaded on the substrate, such as having a loading by area (“areal loading") of at least 0.3 mg/cm 2 .
  • the loading of the first composition or domain is at least 0.5 mg/cm 2 , such as at least 1 mg/cm 2 .
  • the loading of the top coat is low (e.g., relative to the base coat), such as having an areal loading of less than 0.3 mg/cm 2 .
  • the second composition or domain has an areal loading of about 0.001 mg/cm 2 to about 0.3 mg/cm 2 , such as about 0.001 mg/cm 2 to about 0.2 mg/cm 2 , about 0.001 mg/cm 2 to about 0.1 mg/cm 2 , about 0.005 mg/cm 2 to about 0.2 mg/cm 2 , or about 0.01 mg/cm 2 to about 0.1 mg/cm 2 .
  • a film provided herein is a thin film, such as having an overall thickness (e.g., incorporating both the top coat and base coat, but not the substrate) of about 100 micron or less (e.g., about 50 micron or less, about 5 micron to about 25 micron, about 10 micron to 20 micron, or the like).
  • the film has an average thickness of about 5 micron to about 35 micron.
  • the base coat has an average thickness of less than 25 micron (e.g., about 3 micron to about 25 micron, about 3 micron to about 20 micron, or about 5 micron to about 15 micron).
  • the second domain has an average thickness of about 0.1 micron to about 10 micron.
  • the overall film, the base coat, the top coat, or any combination thereof has a thickness variation of less than 50%, e.g., less than 30%, less than 20%), less than 10%>, or the like. Any suitable bulk density is contemplated for overall films, top coats, and base coats, such as about 0.3 grams per cubic cm or more, such as about 0.5 grams per cubic cm or more.
  • a film e.g., with top coat
  • the externally exposed surface comprising at least 90% (e.g., at least 95%, at least 97%), at least 98%>, at least 99%, or the like) carbon inclusion (e.g., second and/or first carbon inclusion/component) by surface area.
  • less than 5% (e.g., less than 3%), less than 2%, less than 1%, or the like) of the surface of the film is comprised of the active electrode material.
  • the carbonaceous components constitute at least 70 wt. %> of the overall film surface. In more specific embodiments, the carbonaceous components constitute at least 80 wt. %> of the film surface. In still more specific embodiments, the carbonaceous components constitute at least 90 wt. %> (e.g., at least 95 wt. %) of the film surface. In some embodiments, the active electrode material or active electrode material-containing inclusions constitute about 50 wt. %> to about 95 wt. %> of the film. In certain embodiments, the carbonaceous components constitute about 5 wt. %> to about 50 wt. %> of the film.
  • inclusions and materials are described as having specific characteristics. It is to be understood that such disclosures include disclosures of a plurality of such inclusions having an average equal to the specific characteristics identified, and vice-versa.
  • electrodes referred to herein as comprising certain characteristics, functionality, and/or component parts includes a disclosure of electrode materials with the same characteristics, functionality, and/or component parts.
  • reference to a solution herein includes liquid compositions wherein inclusion parts are dissolved and/or dispersed therein.
  • Various electrodes and electrode materials were prepared using active materials (silicon or silicon oxide (SiOx)). 3.0 g of GO aqueous suspension was diluted in 5.0 g of DI water. After sonicating the suspension for 1 hr, 60 mg or 120 mg active materials (1 : 1 or 2: 1 weight ratio with graphene oxide) were added. Silicon nanoparticle (70-100nm), SiOx micro size particles (3-10 ⁇ ), silicon micro particles (1 - 3 micron, polycrystalline, 99.99% purity) were utilized as active material in separate examples. The mixture of active material and graphene oxide was then sonicated for another hour and stirred overnight before spraying.
  • active materials silicon or silicon oxide (SiOx)
  • Air-controlled electrospray was applied for manufacture of electrode materials, including directly depositing binder-free electrodes.
  • the electrospray was carried out under ambient condition using a Harvard Apparatus PHD 2000 Infusion syringe pump with a coaxial needle set. Solution was supplied through the inner 17G needle and gas through outer 12G needle.
  • the working voltage was set at 20kV, working distance at 20 cm, solution feeding rate between 0.05 mL min "1 - 0.1 mL min "1 , and gas pressure at 28 psi.
  • the as sprayed active materials/GO were annealed at 400 °C in N 2 atmosphere (tube furnace) for 1 hr to reduce GO, ramp 5°C/min. Direct deposit electrodes were deposited on copper foil.
  • direct deposit anode was prepared using nanofibers having a carbon matrix backbone with silicon nanoparticles embedded therein.
  • the direct deposit anode has a loading of 1.93 mg/cm 2 , a capacity loading of 4.52 mAh/cm 2 , a gravimetric capacity of 2,338 mAh/g, a 1 st cycle Coulombic efficiency of 80%, an electrode density of 0.46 g/cc, and a volumetric energy density of 1061 mAh/cc.
  • Prepared half cells provided the capacity retention set forth in FIG. 10 and the cycling efficiencies set forth in FIG. 11. As illustrated in the figures, despite having a gravimetric capacity of well over 2,000 mAh/g, the materials exhibit very good capacity retention while exhibiting a good 1 st cycle Coulombic efficiency.
  • direct deposited anodes are prepared using silicon (Si) microparticles in an initial Si MP:GO weight ratio of 2: 1, and having a final SiMP:rGO weight ratio of about 4: 1.
  • Half cells are prepared and exhibit an initial capacity of about 1,600 mAh/g (after a few pre-cycles) and have good capacity retention (>85%) after 100 cycles (at ⁇ /g).
  • an extremely high 1 st cycle Coulombic efficiency is achieved (>88%), which is much higher than the 1 st cycle Coulombic efficiency achieved for otherwise similar systems using silicon nanoparticles (about 80% for Si Ps, > 85% is typically required for industrially applications).
  • Full cells were also prepared using the direct deposit anode, using very high loading of anode material (3.16 mg) and 40 mg lithium cobalt oxide (about 20 mg/cm 2 ). Capacity of anode to cathode in the prepared cell is 100:95. As illustrated in FIG. 12, resulting cells exhibit an initial capacity of about 1300 mAh/g with at least 1,000 mAh/g after 65 cycles at 0.5 C. In addition, such cells exhibited a capacity of about 3 mAh/cm 2 , up to about 2 times greater than exhibited in conventional lithium ion battery full cells.
  • direct deposited anodes are prepared using silicon (Si) microparticles in an initial Si MP:GO weight ratio of 8: 1, and having a final SiMP:rGO weight ratio of about 16: 1.
  • Half cells are prepared and exhibit an initial capacity of about 1,600 mAh/g.
  • an extremely high 1 st cycle Coulombic efficiency is achieved (91%).
  • Direct deposit anodes are prepared using low sphericity silicon microparticles and graphene oxide at a 4:3 weight ratio.
  • Direct deposit anodes are prepared by (i) directly depositing an anode from a fluid stock comprising a silicon inclusion (e.g., average size of about 0.5 micron to about 5 micron) and graphene oxide in a silicon inclusion to graphene oxide weight ratio of about 4:3, (ii) depositing a base coat from a fluid stock comprising silicon inclusion (Sil) and graphene oxide (GO) in a SiLGO weight ratio of 2: 1 and a top coat of GO, the total weight of the direct deposit film prior to thermal treatment being 1.22 mg, (iii) depositing a base coat from a fluid stock comprising silicon inclusion (Sil) and graphene oxide (GO) in a SiLGO weight ratio of 2: 1 and a top coat of GO, the total weight of the direct deposit film prior to thermal treatment being 1.22 mg, (iii) depositing
  • Table 1 demonstrates select characteristics of the 4:3 weight ratio anode precursor films prepared prior to thermal treatment:
  • FIG. 6 illustrates the specific capacities of the electrodes thereof.
  • the capacity and retention data is shown in Table 2 below.
  • both anodes having low areal loading top coats performed significantly better than an anode prepared with the same silicon inclusion to graphene oxide weight ratio but without a top coat, whereas the anode having a high areal loading of top coat performed significantly worse, with capacity fading rapidly over just 40 cycles.
  • even the no-top coat 4:3 anode demonstrated significantly better performance (particularly in capacity retention) than did the anodes prepared in Examples 1, 3 and 4, the difference between the materials of Example 5 and Examples 3 and 4 being that the silicon inclusions of Example 5 are less spherical than those of Examples 3 and 4.

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Abstract

L'invention concerne des électrodes à hautes performances, des matériaux d'électrode et des précurseurs correspondants. L'invention concerne également des procédés de génération de celles-ci.
PCT/US2018/021551 2017-03-08 2018-03-08 Électrodes à hautes performances à domaines multiples, matériaux et précurseurs correspondants WO2018165430A1 (fr)

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Citations (5)

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Publication number Priority date Publication date Assignee Title
US20110143018A1 (en) * 2009-10-07 2011-06-16 Shufu Peng Methods and systems for making battery electrodes and devices arising therefrom
US20130344392A1 (en) * 2011-06-30 2013-12-26 Northwestern University Crumpled graphene-encapsulated nanostructures and lithium ion battery anodes made therefrom
JP5590450B2 (ja) * 2009-09-18 2014-09-17 株式会社ニコン 電極材料の成膜方法、及び電極材料成膜用の噴射加工装置
KR20150143224A (ko) * 2014-06-13 2015-12-23 주식회사 엘지화학 리튬-황 전지용 양극 활물질, 이의 제조방법 및 이를 포함한 리튬-황 전지
US20150372291A1 (en) * 2014-06-24 2015-12-24 Hyundai Motor Company Cathode for lithium-sulfur battery

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5590450B2 (ja) * 2009-09-18 2014-09-17 株式会社ニコン 電極材料の成膜方法、及び電極材料成膜用の噴射加工装置
US20110143018A1 (en) * 2009-10-07 2011-06-16 Shufu Peng Methods and systems for making battery electrodes and devices arising therefrom
US20130344392A1 (en) * 2011-06-30 2013-12-26 Northwestern University Crumpled graphene-encapsulated nanostructures and lithium ion battery anodes made therefrom
KR20150143224A (ko) * 2014-06-13 2015-12-23 주식회사 엘지화학 리튬-황 전지용 양극 활물질, 이의 제조방법 및 이를 포함한 리튬-황 전지
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