Abstract: A method of producing a powder mass for a lithium battery, the method comprising: (a) providing a solution containing a sulfonated elastomer dissolved in a solvent or a precursor in a liquid form or dissolved in a solvent; (b) dispersing a plurality of particles of a cathode active material in the solution to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing/curing the precursor to form the powder mass, wherein the powder mass comprises multiple particulates and at least a particulate comprises one or a plurality of particles of a cathode active material being encapsulated by a thin layer of sulfonated elastomer having a thickness from 1 nm to 10 ?m, a fully recoverable tensile strain from 2% to 800%, and a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm at room temperature.

Abstract: The disclosure provides multi-functional composite particulates for a lithium battery, wherein at least one of the composite particulates has a diameter from 100 nm to 50 ?m and comprises a polymer electrolyte matrix comprising a lithium salt dissolved or dispersed in the polymer electrolyte matrix and one or a plurality of primary particles of an anode active material that are encapsulated by, embedded in, dispersed in, or bonded by the polymer electrolyte having a lithium ion conductivity from 10?8 to 5×10?2 S/cm, wherein the primary particles have a diameter or thickness from 0.5 nm to 20 ?m and occupy a weight fraction from 5% to 98% based on the total weight of the composite particulate. Also provided is a method of producing such composite particulates, an anode electrode comprising these particulates, and a lithium cell.

Abstract: The invention provides multiple anode particulates for a lithium battery. At least one of the particulates comprises a core and a thin encapsulating layer encapsulating the core, wherein the core comprises a single or a plurality of porous primary particles of an anode active material (having a pore volume Vpp and a solid volume Va) dispersed or embedded in a porous carbon matrix (a carbon foam matrix) having a pore volume Vp, and the thin encapsulating layer comprises graphene sheets and has a thickness from 1 nm to 10 ?m, an electric conductivity from 10?6 S/cm to 20,000 S/cm and a lithium ion conductivity from 10?8 S/cm to 5×10?2 S/cm and wherein the volume ratio Vp/Va is from 0.1/1.0 to 10/1.0 or the total pore-to-solid ratio (Vp+Vpp)/Va is from 0.3/1.0 to 20/1.0.

Abstract: Provided is an anode particulate or a solid mass of particulates for a lithium battery, the particulate comprising a graphite matrix and a single or a plurality of carbon foam-protected primary particles of an anode active material embedded or dispersed in the graphite matrix, wherein the primary particles of anode active material have a volume Va, the carbon foam contains pores having a pore volume Vp, and the volume ratio Vp/Va is from 0.3/1.0 to 5.0/1.0 and wherein the carbon foam is physically or chemically connected to both the graphite matrix and the primary particles of the anode active material. The carbon foam is preferably reinforced with a high-strength material.

Abstract: Provided is a lithium secondary battery containing an anode, a cathode, a porous separator/electrolyte element disposed between the anode and the cathode, and a cathode-protecting layer bonded or adhered to the cathode, wherein the cathode-protecting layer comprises a lithium ion-conducting polymer matrix or binder and inorganic material particles that are dispersed in or chemically bonded by the polymer matrix or binder and wherein the cathode-protecting layer has a thickness from 10 nm to 100 ?m and the polymer matrix or binder has a lithium-ion conductivity from 10?8 S/cm to 5×10?2 S/cm. Additionally or alternatively, there can be a similarly configured anode-protecting layer adhered to the anode. Such an electrode-protecting layer prevents massive internal shorting from occurring even when the porous separator gets melted, contracted, or collapsed under extreme temperature conditions induced by, for instance, dendrite or nail penetration.

Abstract: A dual electroplating cell comprising: (a) an electrolyte component containing therein ions of a first metal; (b) a porous cathode current collector having surface areas to capture and store metal ions directly thereon, wherein the cathode current collector has a specific surface area greater than 100 m2/g that is in direct contact with said electrolyte; (c) a porous anode current collector having surface areas to capture and store metal ions thereon, wherein the anode current collector has a specific surface area greater than 100 m2/g that is in direct contact with the electrolyte; (d) a porous separator disposed between the anode and the cathode; and (e) an ion source of the first metal disposed in the anode current collector or the cathode current collector and in electronic contact therewith to obtain an open circuit voltage (OCV) from 0.3 volts to 3.5 volts when the cell is made.

Abstract: Provided is a lithium metal secondary battery comprising a cathode, an anode, and a non-solid state electrolyte without a porous separator disposed between the cathode and the anode, wherein the anode comprises: (a) an anode active material layer containing a layer of lithium or lithium alloy, in a form of a foil, coating, or multiple particles aggregated together, as an anode active material; and (b) an anode-protecting layer in physical contact with the anode active material layer, having a thickness from 1 nm to 100 ?m and comprising an elastomer having a fully recoverable tensile elastic strain from 2% to 1,000% and a lithium ion conductivity from 10?8 S/cm to 5×10?2 S/cm when measure at room temperature; wherein the lithium metal secondary battery does not include a lithium-sulfur battery or a lithium-selenium battery.

Abstract: Provided is a humic acid-based coating suspension comprising humic acid, particles of an anti-corrosive pigment or sacrificial metal, and a binder resin dissolved or dispersed in a liquid medium, wherein the humic acid has a weight fraction from 0.1% to 50% based on the total coating suspension weight excluding the liquid medium. Also provided is an object or structure coated at least in part with such a coating.

Abstract: Provided is a method of producing a graphitic film, comprising: (a) providing a suspension of aromatic molecules selected from petroleum heavy oil or pitch, coal tar pitch, a polynuclear hydrocarbon, a halogenated variant thereof, or a combination thereof, dispersed or dissolved in a liquid medium; (b) dispensing and depositing the suspension onto a surface of a supporting substrate to form a wet layer of aromatic molecules, wherein the procedure includes subjecting the suspension to an orientation-inducing stress or strain; (c) partially or completely removing the liquid medium; and (d) heat treating the resulting dried layer at a first temperature selected from 25° C. to 3,200° C. so that the aromatic molecules are merged or fused into larger aromatic molecules to form the graphitic film having graphene domains or graphite crystals, wherein the larger aromatic molecules or graphene planes in the graphene domains or graphite crystals are substantially parallel to each other.

Abstract: Provided is a process for producing a polymer composite film, comprising the steps of: (a) mixing a phthalocyanine compound with a polymer or its precursor and a liquid to form a slurry and forming the slurry into a wet film on a solid substrate, wherein the polymer is preferably selected from the group consisting of polyimide, polyamide, polyoxadiazole, polybenzoxazole, polybenzobisoxazole, polythiazole, polybenzothiazole, polybenzobisthiazole, poly(p-phenylene vinylene), polybenzimidazole, polybenzobisimidazole, and combinations thereof; and (b) removing the liquid from the wet film and, in some embodiments, converting the precursor to the polymer to form the polymer composite film comprising from 0.1% to 50% by weight of the phthalocyanine compound dispersed in the polymer.

Abstract: Provided is a bi-polar electrode for a battery, wherein the bi-polar electrode comprises: (a) a current collector comprising a conductive material foil (e.g. metal foil) having a thickness from 10 nm to 100 ?m and two opposed, parallel primary surfaces, wherein one or both of the primary surfaces is coated with a layer of graphene material having a thickness from 10 nm to 10 ?m; and (b) a negative electrode layer and a positive electrode layer respectively disposed on the two sides of the current collector, each in physical contact with the layer of graphene material or directly with a primary surface of the conductive material foil (if not coated with a graphene material layer). Also provided is a battery comprising multiple (e.g. 2-300) bipolar electrodes internally connected in series. There can be multiple bi-polar electrodes that are connected in parallel.

Abstract: A rechargeable lithium cell comprising a cathode, an anode, an optional ion-permeable membrane disposed between the anode and the cathode, a non-flammable salt-retained liquefied gas electrolyte in contact with the cathode and the anode, wherein the electrolyte contains a lithium salt dissolved in or mixed with a liquefied gas solvent having a lithium salt concentration greater than 1.0 M so that the electrolyte exhibits a vapor pressure less than 1 kPa when measured at 20° C., a vapor pressure less than 60% of the vapor pressure of the liquefied gas solvent alone, a flash point at least 20 degrees Celsius higher than a flash point of the liquefied gas solvent alone, a flash point higher than 150° C.

Abstract: Provided is a method of producing an integral 3D humic acid-carbon hybrid foam, comprising: (A) forming a solid shape of humic acid-polymer particle mixture; and (B) pyrolyzing the solid shape of humic acid-polymer particle mixture to thermally reduce humic acid into reduced humic acid sheets and thermally convert polymer into pores and carbon or graphite that bonds the reduced humic acid sheets to form the integral 3D humic acid-carbon hybrid foam.

Abstract: A method of producing a pre-sulfurized active cathode layer for a rechargeable alkali metal-sulfur cell; the method comprising: (a) Preparing an integral layer of porous graphene structure having a specific surface area greater than 100 m2/g; (b) Preparing an electrolyte comprising a solvent and a sulfur source; (c) Preparing an anode; and (d) Bringing the integral layer and the anode in ionic contact with the electrolyte and imposing an electric current between the anode and the integral layer (serving as a cathode) to electrochemically deposit nano-scaled sulfur particles or coating on the graphene surfaces. The sulfur particles or coating have a thickness or diameter smaller than 20 nm (preferably <10 nm, more preferably <5 nm or even <3 nm) and occupy a weight fraction of at least 70% (preferably >90% or even >95%).

Abstract: A method of producing graphene sheets directly from graphite mineral (graphite rock) powder, comprising: (a) forming an intercalated graphite compound by an electrochemical intercalation procedure conducted in an intercalation reactor, containing (i) a liquid solution electrolyte comprising an intercalating agent and a graphene plane-wetting agent dissolved therein; (ii) a working electrode that contains the graphite material powder as an active material; and (iii) a counter-electrode, and wherein a current is imposed upon the working electrode and counter electrode at a current density sufficient for effecting electrochemical intercalation of the intercalating agent and/or wetting agent into interlayer spacing, wherein the wetting agent is selected from melamine, ammonium sulfate, sodium dodecyl sulfate, Na(ethylenediamine), tetraalkylammonium salts, ammonia, carbamide, hexamethylenetetramine, organic amine, poly(sodium-4-styrene sulfonate), or a combination thereof; and (b) exfoliating and separating the in

Abstract: A black-color polymer composite film comprising a phthalocyanine compound dispersed in a polymer selected from the group consisting of polyimide, polyamide, polyoxadiazole, polybenzoxazole, polybenzobisoxazole, polythiazole, polybenzothiazole, polybenzobisthiazole, poly(p-phenylene vinylene), polybenzimidazole, polybenzobisimidazole, and combinations thereof, wherein the phthalocyanine compound occupies a weight fraction of 0.1% to 50% based on the total polymer composite weight. Preferably, the phthalocyanine compound is selected from copper phthalocyanine, zinc phthalocyanine, tin phthalocyanine, iron phthalocyanine, lead phthalocyanine, nickel phthalocyanine, vanadyl phthalocyanine, fluorochromium phthalocyanine, magnesium phthalocyanine, manganous phthalocyanine, dilithium phthalocyanine, aluminum phthalocyanine chloride, cadmium phthalocyanine, chlorogallium phthalocyanine, cobalt phthalocyanine, silver phthalocyanine, a metal-free phthalocyanine, or a combination thereof.

Abstract: A method of producing a powder mass for a lithium battery, comprising: (a) mixing an inorganic filler and an elastomer or its precursor in a liquid medium or solvent to form a suspension; (b) dispersing a plurality of particles of a cathode active material in the suspension to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing or curing the precursor to form the powder mass, wherein at least a particulate comprises one or a plurality of cathode active material particles being encapsulated by a layer of inorganic filler-reinforced elastomer having a thickness from 1 nm to 10 ?m, a fully recoverable tensile strain from 2% to 500%, and a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm and the inorganic filler has a lithium intercalation potential from 1.1 V to 4.5 V versus Li/Li+.

Abstract: Provided is a method of producing a multivalent metal-ion battery comprising an anode, a cathode, and an electrolyte in ionic contact with the anode and the cathode to support reversible deposition and dissolution of a multivalent metal, selected from Ni, Zn, Be, Mg, Ca, Ba, La, Ti, Ta, Zr, Nb, Mn, V, Co, Fe, Cd, Cr, Ga, In, or a combination thereof, at the anode, wherein the anode contains the multivalent metal or its alloy as an anode active material and the cathode comprises a cathode active layer of graphitic carbon particles or fibers that are coated with a protective material. Such a metal-ion battery delivers a high energy density, high power density, and long cycle life.

Abstract: A method of producing a powder mass for a lithium battery, the method comprising: (a) providing a solution containing a sulfonated elastomer dissolved in a solvent or a precursor in a liquid form or dissolved in a solvent; (b) dispersing a plurality of particles of a cathode active material in the solution to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing/curing the precursor to form the powder mass, wherein the powder mass comprises multiple particulates and at least a particulate comprises one or a plurality of particles of a cathode active material being encapsulated by a thin layer of sulfonated elastomer having a thickness from 1 nm to 10 ?m, a fully recoverable tensile strain from 2% to 800%, and a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm at room temperature.

Abstract: A graphene-enabled hybrid particulate for use as a lithium-ion battery anode active material, wherein the hybrid particulate is formed of a single or a plurality of graphene sheets and a single or a plurality of fine primary particles of a niobium-containing composite metal oxide, having a size from 1 nm to 10 ?m, and the graphene sheets and the primary particles are mutually bonded or agglomerated into the hybrid particulate containing an exterior graphene sheet or multiple exterior graphene sheets embracing the primary particles, and wherein the hybrid particulate has an electrical conductivity no less than 10?4 S/cm and said graphene is in an amount of from 0.01% to 30% by weight based on the total weight of graphene and the niobium-containing composite metal oxide combined.