Abstract: A dust collecting system for single crystal growth system includes an air compressor, a dust collecting device, a first inert gas source, a rotary pump and a scrubber. The air compressor is fluidly connected to an exit pipe of the single crystal growth system. The exit pipe is used to exhaust unstable dust from the single crystal growth system. The dust collecting device is fluidly connecting to the exit pipe to collect the dust oxide. The first inert gas source is fluidly connected to the exit pipe to blow a first inert gas into the exit pipe to compel the dust oxide toward the dust collecting device. The rotary pump is fluidly connected to the dust collecting device. The scrubber is fluidly connected to the rotary pump. The rotary pump transports the residual dust oxide toward the scrubber. The present disclosure further provides a method for collecting dust.

Abstract: A method for producing Si ingot single crystal by NOC growth method including a Si ingot single crystal growing step and a continuous growing step is provided. The growing step includes providing a low temperature region in the Si melt where the Si ingot single crystal is grown along the surface of the Si melt or toward the inside of the Si melt, and the Si ingot single crystal has distribution of a vacancy concentration and an interstitial concentration in which respectively a vacancy concentration and an interstitial concentration vary with a distance from the growth interface; and adjusting a temperature gradient and a growth rate in the Si melt, so that along with the increasing of the distance from the growth interface, the vacancy concentration and the interstitial concentration in the Si ingot single crystal respectively decrease come near to each other.

Abstract: Provided is a battery charging system, comprising (a) at least one charging circuit to charge at least one rechargeable battery cell; and (b) a heating device to provide heat that is transported through a heat spreader element, implemented fully outside the battery cell, to heat up the battery cell to a desired temperature Tc before or during battery charging. The system may further comprise (c) a cooling device in thermal contact with the heat spreader element configured to enable transporting internal heat of the battery cell through the heat spreader element to the cooling device when the battery cell is discharged. Charging the battery at Tc enables completion of the charging of the battery in less than 15 minutes, typically less than 10 minutes, and more typically less than 5 minutes without adversely impacting the battery structure and performance. Also provided is a battery module or pack working with such a system.

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: A lithium- or sodium-ion battery anode layer, comprising a phosphorus material embedded in pores of a solid graphene foam composed of multiple pores and pore walls, wherein (a) the pore walls contain a pristine graphene or a non-pristine graphene material; (b) the phosphorus material contains particles or coating of P or MPy (M=transition metal and 1?y?4) and is in an amount from 20% to 99% by weight based on the total weight of the graphene foam and the phosphorus material combined, and (c) the multiple pores are lodged with particles or coating of the phosphorus material. Preferably, the solid graphene foam has a density from 0.01 to 1.7 g/cm3, a specific surface area from 50 to 2,000 m2/g, a thermal conductivity of at least 100 W/mK per unit of specific gravity, and/or an electrical conductivity no less than 1,000 S/cm per unit of specific gravity.

Abstract: Provided is graphene-encapsulated phosphorus anode particulate for a lithium or sodium ion battery, the particulate comprising: (A) a core comprising one or a plurality of phosphorus material-decorated graphene sheets, wherein the decorated graphene sheets have a length/width from 5 nm to 100 ?m and contain single-layer or few-layer graphene and the phosphorus material is in a form of particles or coating having a diameter or thickness from 0.5 nm to 10 ?m and is selected from red phosphorus, black phosphorus (including phosphorene), violet phosphorus, a metal phosphide, MPy, or a combination thereof, wherein M=Mn, V, Sn, Ni, Cu, Fe, Co, Zn, Ge, Se, Mo, Ga, In, or an alloy thereof, and y=1-4; and (B) an encapsulating shell that embraces or encapsulates the core, wherein the encapsulating shell comprises multiple graphene sheets and have a thickness from 0.34 nm to 5 ?m.

Abstract: An electrochemical battery cell comprising an anode having a primary anode active material, a cathode, and an ion-conducting electrolyte, wherein the cell has an initial output voltage, Vi, measured at 10% depth of discharge (DoD), selected from a range from 0.3 volts to 0.8 volts, and a final output voltage Vf measured at a DoD no greater than 90%, wherein a voltage variation, (Vi?Vf)/Vi, is no greater than ±10% and the specific capacity between Vi and Vf is no less than 100 mAh/g or 200 mAh/cm3 based on the cathode active material weight or volume, and wherein the primary anode active material is selected from lithium (Li), sodium (Na), potassium (K), magnesium (Mg), aluminum (Al), zinc (Zn), titanium (Ti), manganese (Mn), iron (Fe), vanadium (V), cobalt (Co), nickel (Ni), a mixture thereof, an alloy thereof, or a combination thereof.

Abstract: Provided is anode active material for use in a lithium ion battery, wherein the anode active material is capable of reversibly storing lithium ions therein up to a maximum lithium storage capacity Cmax during a charge or discharge of the battery and the anode active material comprises an amount of solid-electrolyte interphase (SEI) on a surface or in an internal structure of the anode active material wherein the SEI is pre-formed prior to incorporating the anode active material in an anode electrode of the battery. Also provided is a method of producing the pre-formed SEI substances in the anode material; e.g. through repeated lithiation/delithiation procedures.

Abstract: Provided is a rechargeable battery comprising an anode, a cathode, an electrolyte disposed between the anode and the cathode, a protective housing that at least partially encloses the anode, the cathode and the electrolyte, a heat-spreader element disposed at least partially inside the protective housing and configured to receive heat from an external heat source at a desired heating temperature Th to heat up the battery to a desired temperature Tc for battery charging. Preferably, the heat-spreader element does not receive an electrical current from an external circuit (e.g. battery charger) to generate heat for resistance heating of the battery. Charging the battery at Tc enables completion of the battery in less than 15 minutes, typically less than 10 minutes, and more typically less than 5 minutes without adversely impacting the battery structure and performance.

Abstract: Provided is a battery charging system comprising (a) at least one charging circuit to charge at least one rechargeable battery cell; (b) a heat source to provide heat that is transported through a heat spreader element, implemented fully or partially inside said at least one battery cell, to heat up the battery cell to a desired temperature Tc before or during battery charging; and (c) cooling means in thermal contact with the heat spreader element configured to enable transporting internal heat of the battery cell through the heat spreader element to the cooling means when the battery cell is discharged. Charging the battery at Tc enables completion of the battery in less than 15 minutes, typically less than 10 minutes, and more typically less than 5 minutes without adversely impacting the battery structure and performance.

Abstract: A rechargeable lithium cell comprising a cathode, an anode, a non-flammable electrolyte, wherein the electrolyte contains a lithium salt dissolved in a liquid solvent having a lithium salt concentration from 0.01 M to 10 M so that the electrolyte exhibits a vapor pressure less than 0.01 kPa when measured at 20° C., a vapor pressure less than 60% of the vapor pressure of the liquid solvent alone, a flash point at least 20 degrees Celsius higher than a flash point of the liquid solvent alone, a flash point higher than 200° C., or no flash point, wherein the liquid solvent contains a cooking oil selected from palm oil, palm olein, coconut oil, corn oil, soybean oil, cottonseed oil, peanut oil, sunflower oil, canola oil, rice bran oil, olive oil, sesame oil, safflower oil, avocado oil, flaxseed oil, grapeseed oil, walnut oil, almond oil, lard, or a combination thereof.

Abstract: Provided is a rechargeable battery system comprising at least a battery cell and an external cooling means, wherein the battery cell comprises an anode, a cathode, an electrolyte disposed between the anode and the cathode, a protective housing that at least partially encloses the anode, the cathode and the electrolyte, and at least one heat-spreader element disposed partially or entirely inside the protective housing and wherein the external cooling means is in thermal contact with the heat spreader element configured to enable transporting internal heat of the battery through the heat spreader element to the external cooling means. Also provided is a method of operating a rechargeable battery system, the method comprising implementing a heat spreader element in one or each of a plurality of battery cells and bringing the heat spreader element in thermal contact with one or a plurality of external cooling means.

Abstract: Provided is a rechargeable battery comprising an anode, a cathode, an electrolyte disposed between the anode and the cathode, a protective housing that at least partially encloses the anode, the cathode and the electrolyte, a heat-spreader element disposed at least partially inside the protective housing and configured to receive heat from an external heat source at a desired heating temperature Th to heat up the battery to a desired temperature Tc for battery charging. Preferably, the heat-spreader element does not receive an electrical current from an external circuit (e.g. battery charger) to generate heat for resistance heating of the battery. Charging the battery at Tc enables completion of the battery in less than 15 minutes, typically less than 10 minutes, and more typically less than 5 minutes without adversely impacting the battery structure and performance.

Abstract: Provided is a prelithiated anode active material particle for use in a lithium-ion battery, the particle is capable of reversibly storing lithium ions therein during a charge or discharge of the battery and comprises an amount of lithium from 1% to 100% of a maximum lithium content that can be contained in the anode active material particle, having a first lithium concentration C1 near a particle surface and a second lithium concentration C2 inside the particle and away from the particle surface and wherein C1<C2.

Abstract: An electrochemical battery cell comprising an anode having a primary anode active material, a cathode, and an ion-conducting electrolyte, wherein the cell has an initial output voltage, Vi, measured at 10% depth of discharge (DoD), selected from a range from 0.3 volts to 0.8 volts, and a final output voltage Vf measured at a DoD no greater than 90%, wherein a voltage variation, (Vi?Vf)/Vi, is no greater than ±10% and the specific capacity between Vi and Vf is no less than 100 mAh/g or 200 mAh/cm3 based on the cathode active material weight or volume, and wherein the primary anode active material is selected from lithium (Li), sodium (Na), potassium (K), magnesium (Mg), aluminum (Al), zinc (Zn), titanium (Ti), manganese (Mn), iron (Fe), vanadium (V), cobalt (Co), nickel (Ni), a mixture thereof, an alloy thereof, or a combination thereof.

Abstract: Provided is graphene-embraced anode particulate for a lithium battery, the particulate comprising: (A) a core comprising one or a plurality of anode active material-decorated carbon or graphite particles, wherein the carbon or graphite particles have a diameter or thickness from 500 nm to 50 ?m and the anode active material, in a form of particles or coating having a diameter or thickness from 0.5 nm to 2 ?m, is bonded to or embedded into surfaces of the carbon or graphite particles; and (B) an embracing shell embracing or encapsulating the core, wherein the embracing shell comprises multiple graphene sheets and have a thickness from 0.34 nm to 5 ?m.

Abstract: Provided is method of producing graphene-embraced anode particulates for a lithium battery, the method comprising: (A) providing anode active material-decorated carbon or graphite particles, wherein the carbon or graphite particles have a diameter or thickness from 500 nm to 50 ?m and the anode active material, in a form of particles or coating having a diameter or thickness from 0.5 nm to 2 ?m, is bonded to surfaces of the carbon or graphite particles; and (B) embracing the anode active material-decorated carbon or graphite particles with a shell comprising multiple graphene sheets to produce the graphene-embraced anode particulates.

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 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: A process for producing a graphene/Si nanowire hybrid material, comprising: (a) dispersing catalyst metal-coated Si particles, graphene sheets, and an optional blowing agent in a liquid medium to form a graphene/Si dispersion; (b) dispensing and depositing the dispersion onto a supporting substrate to form a wet layer and removing the liquid medium from the wet layer to form a dried layer of graphene/Si mixture material; (c) exposing the dried layer to a high temperature environment, from 300° C. to 2,000° C., to induce volatile gas molecules from graphene sheets or to activate the blowing agent for producing the graphene foam and to enable a catalyst metal-catalyzed growth of multiple Si nanowires emanated from Si particles as a feed material in pores of the foam to form a layer of the hybrid material; and (d) operating a mechanical breaking means to produce the Si nanowire/graphene hybrid material in a powder mass form.