Abstract: Provided is an impact-transfer method of producing multiple anode particulates for a lithium battery, the method comprising: (a) mixing multiple particles of a graphitic material, multiple polymer-coated porous primary anode active material particles, with or without the presence of externally added milling balls or beads, to form a mixture in an impacting chamber of an energy impacting apparatus; (b) operating the energy impacting apparatus for peeling off graphene sheets from the particles of graphitic material and transferring the peeled graphene sheets to surfaces of the polymer-coated anode active material particles to produce particulates of graphene-encapsulated polymer-coated porous anode active material particles; (c) recovering the particulates from the impacting chamber and separating the particles of ball-milling media from the particulates; and (d) thermally converting the polymer in the polymer-coated particles into a carbon foam to obtain porous, graphene-encapsulated carbon foam-protected anod

Abstract: Provided is a lithium secondary battery, comprising a cathode, an anode, and a porous separator or electrolyte, wherein the anode comprises: (a) an anode active 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; (b) a first anode-protecting layer having a thickness from 1 nm to 100 ?m, a specific surface area greater than 50 m2/g and comprising a thin layer of electron-conducting material selected from graphene sheets, carbon nanotubes, carbon nanofibers, carbon or graphite fibers, expanded graphite flakes, metal nanowires, conductive polymer fibers, or a combination thereof, and (c) a second anode-protecting 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.

Abstract: A lithium battery cathode layer containing multiple particles or coating of a cathode active material (metal fluoride or metal chloride) and a layer of exfoliated graphite worms composed of interconnected graphite flakes and inter-flake pores, wherein (a) the graphite worms are selected from exfoliated natural graphite, exfoliated artificial graphite, exfoliated meso carbon micro-beads, exfoliated coke, exfoliated meso-phase pitch, exfoliated carbon or graphite fiber, or a combination thereof; (b) the cathode active material particles or coating has a size from 0.4 nm to 10 ?m, and is in an amount from 1% to 99% by weight based on the total weight of graphite worms and the cathode active material combined; and (c) some of the pores are lodged with particles or coating of the cathode active material.

Abstract: Provided is a lithium secondary battery, comprising a cathode, an anode, and a porous separator or electrolyte, wherein the anode comprises: (a) an anode active 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; (b) a first anode-protecting layer having a thickness from 1 nm to 100 ?m (preferably <1 ?m and more preferably <100 nm) and comprising a lithium ion-conducting material having a lithium ion conductivity from 10?8 S/cm to 5×10?2 S/cm; and (c) a second anode-protecting 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.

Abstract: A surface-enabled, metal ion-exchanging battery device comprising a cathode, an anode, a porous separator, and a metal ion-containing electrolyte, wherein the metal ion is selected from aluminum (Al), gallium (Ga), indium (In), tin (Sn), lead (Pb), or bismuth (Bi), and at least one of the electrodes contains therein a metal ion source prior to the first charge or discharge cycle of the device and at least the cathode comprises a functional material or nanostructured material having a metal ion-capturing functional group or metal ion-storing surface in direct contact with the electrolyte. This energy storage device has a power density significantly higher than that of a lithium-ion battery and an energy density dramatically higher than that of a supercapacitor.

Abstract: Provided is a lithium-selenium battery, comprising a cathode, an anode, and a porous separator/electrolyte assembly, wherein the anode comprises an anode active layer containing lithium or lithium alloy as an anode active material, and the cathode comprises a cathode active layer comprising a selenium-containing material, wherein an anode-protecting layer is disposed between the anode active layer and the separator/electrolyte and/or a cathode-protecting layer is disposed between the cathode active layer and the separator/electrolyte; the protecting layer contains a composite comprising from 0.01% to 50% by weight of a conductive reinforcement material dispersed in a sulfonated elastomeric matrix material and has a thickness from 1 nm to 100 ?m, a fully recoverable tensile strain from 2% to 500%, a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm, and an electrical conductivity from 10?7 S/cm to 100 S/cm.

Abstract: Provided is lithium secondary battery comprising a cathode, an anode, and an electrolyte or separator-electrolyte assembly disposed between the cathode and the anode, wherein the anode comprises: (a) a foil or coating of lithium or lithium alloy as an anode active material; and (b) a thin layer of a high-elasticity polymer having a recoverable tensile strain no less than 5%, a lithium ion conductivity no less than 10?6 S/cm at room temperature, and a thickness from 1 nm to 10 ?m, wherein the high-elasticity polymer contains an ultrahigh molecular weight polymer having a molecular weight from 0.5×106 to 9×106 g/mole and is disposed between the lithium or lithium alloy and the electrolyte or separator-electrolyte assembly.

Abstract: A process for producing a solid graphene foam composed of multiple pores and pore walls The process comprises: (a) preparing a graphene dispersion having a graphene material dispersed in a liquid medium, which contains an optional blowing agent; (b) dispensing and depositing the graphene dispersion onto a supporting substrate to form a wet layer of graphene material having a preferred orientation; (c) partially or completely removing the liquid medium from the wet layer of graphene material to form a dried layer of graphene material having a content of non-carbon elements no less than 5% by weight (including blowing agent weight); and (d) heat treating the layer of graphene material at a first heat treatment temperature from 80° C. to 3,200° C. at a desired heating rate sufficient to induce volatile gas molecules from the non-carbon elements or to activate the blowing agent for producing the graphene foam having a density from 0.01 to 1.7 g/cm3 or a specific surface area from 50 to 3,000 m2/g.

Abstract: A lithium super-battery cell comprising: (a) A cathode comprising a cathode active material having a surface area to capture or store lithium thereon, wherein the cathode active material is not a functionalized material and does not bear a functional group; (b) An anode comprising an anode current collector; (c) A porous separator disposed between the two electrodes; (d) A lithium-containing electrolyte in physical contact with the two electrodes, wherein the cathode active material has a specific surface area of no less than 100 m2/g being in direct physical contact with the electrolyte to receive lithium ions therefrom or to provide lithium ions thereto; and (e) A lithium source implemented at one or both of the two electrodes prior to a first charge or a first discharge cycle of the cell. This new generation of energy storage device exhibits the best properties of both the lithium ion battery and the supercapacitor.

Abstract: Provided is a lithium secondary battery, comprising a cathode, an anode, and a porous separator or electrolyte, wherein the anode comprises: (a) an anode active 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 of a conductive sulfonated elastomer composite, disposed between the anode active layer and the separator/electrolyte; wherein the composite has from 0.01% to 40% by weight of a conductive reinforcement material and from 0.01% to 40% by weight of an inorganic filler dispersed in a sulfonated elastomeric matrix material and the protecting layer has a thickness from 1 nm to 100 ?m, a fully recoverable tensile strain from 2% to 500%, a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm, and an electrical conductivity from 10?7 S/cm to 100 S/cm.

Abstract: Provided is a lithium-ion battery containing an anode, a cathode, a porous separator, and an electrolyte, wherein the cathode comprises particles of a cathode active material that are packed together to form a cathode active material layer having interstitial spaces to accommodate a lithium ion receptor disposed therein and configured to receive lithium ions from the anode and enable lithium ions to enter the particles in a time-delayed manner, wherein the receptor comprises lithium-capturing groups selected from (a) redox forming species that reversibly form a redox pair with a lithium ion when the battery is charged; (b) electron-donating groups interspaced between non-electron-donating groups; (c) anions and cations wherein the anions are less or more mobile than the cations; (d) chemical reducing groups that partially reduce lithium ions from Li+1 to Li+?, wherein 0<?<1; (e) an ionic liquid; or (f) a combination thereof.

Abstract: Provided is an anode active material layer for a lithium battery. This layer comprises multiple particulates of an anode active material, wherein at least a particulate is composed of one or a plurality of particles of a high-capacity anode active material being encapsulated by a thin layer of elastomeric material that has a lithium ion conductivity no less than 10?7 S/cm (preferably no less than 10?5 S/cm) at room temperature and an encapsulating shell thickness from 1 nm to 10 ?m, and wherein the high-capacity anode active material (e.g. Si, Ge, Sn, SnO2, Co3O4, etc.) has a specific capacity of lithium storage greater than 372 mAh/g (the theoretical lithium storage limit of graphite).

Abstract: Provided is a lithium ion battery that exhibits a significantly improved specific capacity and much longer charge-discharge cycle life. In one preferred embodiment, the battery comprises a cathode, an anode, an electrolyte in ionic contact with both the cathode and the anode, and an optional separator disposed between the cathode and the anode, wherein, prior to the battery being assembled, the anode comprises (a) an anode active material layer composed of fine particles of a first anode active material having an average size from 1 nm to 10 ?m, an optional conductive additive, and an optional binder that bonds the fine particles and the conductive additive together to form the anode active material layer having structural integrity and (b) a layer of lithium metal or lithium metal alloy having greater than 80% by weight of lithium therein, wherein the layer of lithium metal or lithium metal alloy is in physical contact with the anode active material layer.

Abstract: A continuous process for producing a surface-metalized polymer article, comprising: (a) continuously immersing a polymer article into a graphene dispersion comprising multiple graphene sheets dispersed in a liquid medium for a period of immersion time and then retreating the polymer article from the dispersion, enabling deposition of graphene sheets onto a surface of the polymer article to form a graphene-attached polymer article; (b) continuously moving the graphene-attached polymer article into a drying or heating zone to enable bonding of graphene sheets to said surface to form a graphene-covered polymer article; and (c) continuously moving the graphene-covered polymer article into a metallization zone where a layer of a metal is chemically, physically, electrochemically or electrolytically deposited onto a surface of the graphene-covered polymer article to form the surface-metalized polymer article. Step (a) may be preceded by a surface treatment of the polymer article.

Abstract: A highly oriented humic acid film, comprising multiple humic acid (HA) or chemically functionalized humic acid (CHA) sheets that are chemically bonded or merged and are substantially parallel to one another, wherein the film has a thickness from 5 nm to 500 ?m, a physical density no less than 1.3 g/cm3, hexagonal carbon planes with an inter-planar spacing d002 of 0.4 nm to 1.3 nm as determined by X-ray diffraction, and a non-carbon element content or oxygen content lower than 5% by weight.

Abstract: Provided is graphene-embraced particulate for use as a lithium-ion battery anode active material, wherein the particulate comprises primary particle(s) of an anode active material and multiple sheets of a first graphene material overlapped together to embrace or encapsulate the primary particle(s) and wherein a single or a plurality of graphene-encapsulated primary particles, along with an optional conductive additive, are further embraced or encapsulated by multiple sheets of a second graphene material, wherein the first graphene and the second graphene material is each in an amount from 0.01% to 20% by weight and the optional conductive additive is in an amount from 0% to 50% by weight, all based on the total weight of the particulate. Also provided are an anode and a battery comprising multiple graphene-embraced particulates.

Abstract: Provided is a lithium secondary battery, comprising a cathode, an anode, and a porous separator or electrolyte disposed between the cathode and the anode, wherein the anode comprises: (a) an anode active 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 of a conductive sulfonated elastomer composite, disposed between the anode active layer and the separator/electrolyte; wherein the composite has from 0.01% to 50% by weight of a conductive reinforcement material dispersed in a sulfonated elastomeric matrix material and the protecting layer has a thickness from 1 nm to 100 ?m, a fully recoverable tensile strain from 2% to 500%, a lithium ion conductivity from 10?7 S/cm to 5×10?2 S/cm, and an electrical conductivity from 10?7 S/cm to 100 S/cm.

Abstract: Provided is a method of producing a mass of graphene-embraced particulates, comprising (A) peeling off graphene sheets from graphite particles and directly or indirectly transferring these graphene sheets to encapsulate primary particles of an anode active material using an energy-impact device, wherein multiple graphene sheets are overlapped together to embrace or encapsulate a primary particle; and (B) combining the resulting graphene-encapsulated primary particles with additional graphene sheets, along with an optional conductive additive, to form graphene-embraced particulates. Also provided are an anode electrode comprising multiple graphene-embraced particulates and a battery comprising such an anode electrode.

Abstract: Provided is a method of manufacturing a rechargeable alkali metal-selenium cell, comprising: (a) providing a cathode and an optional cathode current collector to support the cathode; (b) providing an alkali metal anode and an optional anode current collector to support said anode; and (c) providing an electrolyte in contact with the anode and the cathode and an optional separator electrically separating the anode and the cathode; wherein the cathode contains multiple particulates of a selenium-containing material wherein at least one of the particulates comprises one or a plurality of selenium-containing material particles being embraced or encapsulated by a thin layer of a high-elasticity polymer having a recoverable tensile strain from 5% to 1,000% when measured without an additive or reinforcement, a lithium ion conductivity no less than 10?7 S/cm at room temperature, and a thickness from 0.5 nm to 10 ?m.

Abstract: A method of producing a pre-selenized (selenium-preloaded) active cathode layer for a rechargeable alkali metal-selenium cell; the method comprising: (a) preparing an integral layer of mesoporous structure having pore sizes from 0.5 nm to 50 nm (preferably from 0.5 nm to 5 nm) and a specific surface area from 100 to 3,200 m2/g; (b) preparing an electrolyte comprising a solvent and a selenium 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 nanoscaled selenium particles or coating on the graphene surfaces. The selenium particles or coating have a thickness or diameter smaller than 20 nm (preferably <10 nm, more preferably <5 nm or even <3 nm) and preferably occupy a weight fraction of at least 70% (preferably >90% or even >95%).