Abstract: An electrolyte for a lithium battery, the electrolyte including a compound represented by Formula 1; a nonaqueous organic solvent; and a lithium salt. wherein, in Formula 1, X, Ya, Z, R1, and R2 are as defined.

Abstract: There is provided a negative electrode for a secondary battery that can provide a secondary battery having high charge and discharge efficiency, and a high capacity retention rate in charge and discharge cycles. A negative electrode for a secondary battery according to this exemplary embodiment contains scale-like graphite, a fluorine-based resin, and an imide-based resin. A method for manufacturing a negative electrode for a secondary battery according to this exemplary embodiment includes applying a negative electrode slurry containing scale-like graphite, a fluorine-based resin, an imide-based resin, and a solvent for dissolving the fluorine-based resin and the imide-based resin to a negative electrode current collector; and heat-treating the negative electrode current collector at a temperature of 100° C. or more and 150° C. or less.

Abstract: A system and method are presented for the large scale synthesis of metal cyanometallates (MCMs). First and second precursor solutions are added to a main reactor, where the first precursor includes M1 metal cations. The second precursor solution includes AX?M2(CN)Z?, where M1 and M2 are from a first group of metals and A is from a second group of metals including alkali or alkaline earth metals. In response to stirring the first and second precursors, MCM particles are formed with the formula AXM1NM2M(CN)Z.d[H2O]ZEO.e[H2O]BND, in solution. In response to aging in the secondary reactor, the size of the MCM particles is increases. The aged MCM particles in solution are then transferred to a separation tank, where the aged MCM particles are filtered from the solution and collected. The solution reclaimed from the separation tank back is added back into the main reactor.

Abstract: The invention concerns flow batteries comprising: a first half-cell comprising: (i) a first aqueous electrolyte comprising a first redox active material; and a first carbon electrode in contact with the first aqueous electrolyte; (ii) a second half-cell comprising: a second aqueous electrolyte comprising a second redox active material; and a second carbon electrode in contact with the second aqueous electrolyte; and (iii) a separator disposed between the first half-cell and the second half-cell; the first half-cell having a half-cell potential equal to or more negative than about ?0.3 V with respect to a reversible hydrogen electrode; and the first aqueous electrolyte having a pH in a range of from about 8 to about 13, wherein the flow battery is capable of operating or is operating at a current density at least about 25 mA/cm2.

Abstract: A method for obtaining salts of bicyclic imidazole compounds (V) having general structural formulae in which A represents a monovalent cation, X represents independently a carbon atom, an oxygen atom, a sulphur atom or a nitrogen atom. Also, the associated production method and to the use thereof, in particular as an electrolyte component for batteries.

Abstract: A method for fabricating a paper lithium ion cell including depositing a first lithium-metal oxide composition onto a first electrically conducting microfiber paper substrate to define a cathode, depositing a second, different lithium-metal oxide composition onto a second electrically conducting coated microfiber paper substrate to define an anode, separating the cathode and the anode with a barrier material, infusing the cathode and the anode with electrolytes, and encapsulating the anode, the cathode, and the barrier material in a housing.

Abstract: Provided herein are functionally substituted fluoropolymers suitable for use in liquid and solid non-flammable electrolyte compositions. The functionally substituted fluoropolymers include perfluoropolyethers (PFPEs) having high ionic conductivity. Also provided are non-flammable electrolyte compositions including functionally substituted PFPEs and alkali-metal ion batteries including the non-flammable electrolyte compositions.

Abstract: A lithium-ion battery containing: a positive electrode, a negative electrode, an electrolyte comprising: an organic solvent chosen from the group comprising carbonates, linear esters of a saturated acid, or a mixture thereof, an additive capable of forming a passivation film on the surface of the negative electrode, at least one lithium salt, at least one ionic liquid for which the percentage by weight in the electrolyte is greater than or equal to 20% and less than 50%; a separator for which the apparent contact angle between the surface thereof and the electrolyte is less than 20°.

Abstract: In one embodiment, an electrochemical cell includes a negative electrode, a porous separator adjacent to the negative electrode, and a positive electrode separated from the negative electrode by the porous separator, the positive electrode including a conductive matrix and a plurality of insulator particles extending from the conductive matrix.

Abstract: Disclosed is a positive electrode for a non-aqueous electrolyte secondary battery, including a current collector and a mixture layer attached thereto. The mixture layer includes an active material including particles of a first active material, i.e., a lithium-manganese composite oxide, and particles of a second active material, i.e., a lithium-nickel composite oxide. A proportion of the first active material particles in the active material is 51 vol % to 90 vol %. A volume-based particle size distribution of the first active material particles has a first peak on a larger particle side and a second peak on a smaller particle side. A first particle size D1 corresponding to the first peak is 2.5 to 5 times larger than a second particle size D2 corresponding to the second peak. A volume-based particle size distribution of the second active material particles has a third peak corresponding to a third particle size D3 satisfying D1>D3>D2.

Abstract: A galvanic cell having a lithium metal or an alloy comprising a lithium metal as anode material, having an electrolyte comprising lithium bis(oxalate)borate and at least one other lithium complex salt in an aprotic solvent or solvent mixture, in the ratio of lithium complex salt in the conducting salt equals 0.01 to 20 mol %.

Abstract: Provided is a flame-retardant electrolytic capacitor which is capable of maintaining flame-retardant effect even after a prolonged period of time. This is an electrolytic capacitor comprising an anode foil that is provided with an oxide film on the surface, a cathode foil, a separator, and an electrolytic solution that contains a solute in a solvent, wherein a phosphoric acid ester amide represented by the following general formula (1) is contained in the electrolytic solution: in which n is 1 or 2, and R1 and R2 each independently represent a linear or branched alkyl group having 1 to 10 carbon atoms, and Rf represents a linear or branched fluoroalkyl group having 1 to 10 carbon atoms or a linear or branched alkyl group having 1 to 10 carbon atoms).

Abstract: Methods are presented for synthesizing metal cyanometallate (MCM). A first method provides a first solution of AXM2Y(CN)Z, to which a second solution including M1 is dropwise added. As a result, a precipitate is formed of ANM1PM2Q(CN)R.FH2O, where N is in the range of 1 to 4. A second method for synthesizing MCM provides a first solution of M2C(CN)B, which is dropwise added to a second solution including M1. As a result, a precipitate is formed of M1[M2S(CN)G]1/T. DH2O, where S/T is greater than or equal to 0.8. Low vacancy MCM materials are also presented.

Abstract: A protective fabric or material includes a base material and at least one inorganic filler selected from the group consisting of a chemical decontamination agent, a biological decontamination agent, an electromagnetic radiation shielding agent, an antimicrobial agent, a self-decontaminating agent, a decontamination catalyst, a carbon dioxide absorbing agent, and a combination thereof.

Abstract: A battery is provided with a hexacyanometallate cathode. The battery cathode is made from hexacyanometallate particles overlying a current collector. The hexacyanometallate particles have the chemical formula AXM1MM2N(CN)Z.d[H2O]ZEO.e[H2O]BND, where A is a metal from Groups 1A, 2A, or 3A of the Periodic Table, where M1 and M2 are each a metal with 2+ or 3+ valance positions, where “ZEO” and “BND” indicate zeolitic and bound water, respectively, where d is 0, and e is greater than 0 and less than 8. The anode material may primarily be a material such as hard carbon, soft carbon, oxides, sulfides, nitrides, silicon, metals, or combinations thereof. The electrolyte is non-aqueous. A method is also provided for fabricating hexacyanometallate with no zeolitic water content in response to dehydration annealing at a temperature of greater than 120 degrees C. and less than 200 degrees C.

Abstract: A method for fabricating a paper lithium ion cell including depositing a first lithium-metal oxide composition onto a first electrically conducting microfiber paper substrate to define a cathode, depositing a second, different lithium-metal oxide composition onto a second electrically conducting coated microfiber paper substrate to define an anode, separating the cathode and the anode with a barrier material, infusing the cathode and the anode with electrolytes, and encapsulating the anode, the cathode, and the barrier material in a housing.

Abstract: A method for stabilizing a solution that contains LiPF6 by increasing thermal stability of LiPF6 without changing the structure thereof; an electrolyte solution for nonaqueous secondary batteries, which has increased thermal stability; and a nonaqueous secondary battery which has increased thermal stability. The solution containing LiPF6 contains a phosphoric acid ester amide in such an amount that the molar ratio of the phosphoric acid ester amide relative to LiPF6 is 0.001-2.

Abstract: The present invention provides an aligned carbon nanotube assembly constituted of carbon nanotubes each having a defective pore on its side surface, a method of manufacturing the aligned carbon nanotube assembly, a carbon-based electrode, and a power storage device. The aligned carbon nanotube assembly is formed by aggregating a large number of carbon nanotubes aligned in parallel along the same direction and having parallel orientation. In such a state that the aligned carbon nanotube assembly remains grown, the carbon nanotube constituting the aligned carbon nanotube assembly has a defective pore on its side surface. In a raman spectrum of the aligned carbon nanotube assembly in a Raman spectrometric method, when intensity of scattered light in D-band is represented by ID and intensity of scattered light in G-band is represented by IG, an ID/IG ratio is not less than 0.80.

Abstract: Electrolyte solutions including additives or combinations of additives that provide low temperature performance and high temperature stability in lithium ion battery cells.

Abstract: An optimal material composition that allows for the purification of at least one feed component from a fluid feed stream such that the adsorbent has an oxygen capacity of at least 10 weight percent is described. More specifically, the material is an adsorbent for purification of a fluid feed stream having an oxygen to argon selectivity greater than or equal to a ratio of 3:1 and an oxygen capacity of greater than or equal to 10 weight percent, wherein the oxygen capacity is measured at a pressure in the range of about 9-10 Torr and a temperature of 77 degrees Kelvin after 4 hours of equilibration time and wherein the oxygen to argon selectivity is obtained by dividing the oxygen capacity by the argon capacity of the adsorbent measured at a pressure in the range of about 697-700 Torr and a temperature of 87 degrees Kelvin after 8 hours of equilibration time. The adsorption capacities are measured on a pure component basis.

Abstract: A method is provided for fabricating a cyanometallate cathode battery. The method provides a cathode of AXM1YM2Z(CN)N.MH2O, where “A” is selected from a first group of metals, and where M1 and M2 are transition metals. The method provides an anode and a metal ion-permeable membrane separating the anode from the cathode. A third electrode is also provided including “B” metal ions selected from the first group of metals. Typically, the first group of metals includes alkali and alkaline metals. The method intercalates “B” metal ions from the third electrode to the anode, the cathode, or both the anode and cathode to form a completely fabricated battery. In one aspect, a solid electrolyte interface (SEI) layer including the “B” metal ions overlies a surface of the anode, the cathode, or both the anode and cathode. A cyanometallate cathode battery is also provided.

Abstract: A carbon-coated active material composite, an electrode and a lithium ion battery capable of improving electron conductivity and lithium ion conductivity when an electrode active material having a carbonaceous film formed on the surface is used as an electrode material are provided. In the carbon-coated active material composite, charge migration of lithium ions occurs at an interface between a carbonaceous film and an electrode active material, an activation energy of an insertion and removal reaction of lithium ions at an interface between the carbon-coated active material composite and an electrolytic solution is 45 kJ/mol to 85 kJ/mol, a value of a carbon supported amount to a specific surface area of particles of an electrode active material is 0.01 to 0.5, and the activation energy is measured using an electrolyte solution obtained by mixing ethylene carbonate and diethyl carbonate at a 1:1 ratio.

Abstract: A method is provided for charging a supercapacitor. The method initially provides a supercapacitor with a metal cyanometallate (MCM) particle anode, an electrolyte including a salt (DB) made up of cations (D+) anions (B?), and a cathode including carbonaceous materials (?). The method connects an external charging device between the anode and cathode, and the charging device supplies electrons to the anode and accepting electrons from the cathode. In response to the charging device, cations are inserted into the anode while anions are absorbed on the surface of the cathode. A supercapacitor device is also presented.

Abstract: The manufacturing method of the invention includes the steps of: providing a positive electrode and a negative electrode (S10), a sodium ingredient being included in either the positive electrode or the negative electrode; producing an electrode assembly from the provided positive electrode and negative electrode (S20); producing a battery assembly in which the electrode assembly is housed in a battery case (S30); injecting a nonaqueous electrolyte solution into the battery case (S40), the nonaqueous electrolyte solution including at least lithium bis(oxalato)borate, a fluorophosphate compound, a carbonate solvent and an ether solvent, and the amount of ether solvent included in the nonaqueous electrolyte solution being less than 10 vol % when the amount of nonaqueous solvent included in the nonaqueous electrolyte solution is set to 100 vol %; and charging and discharging the battery assembly (S50).

Abstract: A sulfur based active material has a core-shell structure including a hollow core and a porous carbon shell surrounding the hollow core. Sulfur is present in a portion of the hollow core. A polymer shell coating is formed on the porous carbon shell. The polymer shell coating includes nitrogen atoms that bond to carbon atoms of the porous carbon shell so that the porous carbon shell is a nitrogen-confused porous carbon shell.

Abstract: The object is to provide a secondary battery with higher performance, and especially to provide a secondary battery having low impedance. An exemplary embodiment of the invention is a secondary battery, comprising an electrode assembly in which a positive electrode and a negative electrode are oppositely disposed, an electrolyte liquid, and a package which encloses the electrode assembly and the electrolyte liquid inside; wherein the negative electrode is formed by binding a negative electrode active substance to a negative electrode collector with a negative electrode binder; and wherein the electrolyte liquid comprises a fluorine-containing cyclic ether compound.

Abstract: The electrode active material includes a carbon material having a volume of macropores with 50 to 400 nm pore diameters of 0.05 to 0.40 cc/g. The carbon material may be a composite carbon material that contains a carbon material forming a core, and a coating carbon material covering at least part of the core-forming carbon material.

Abstract: A method is provided for forming a rechargeable metal-ion battery with a non-aqueous hybrid ion electrolyte. The method provides a transition metal hexacyanometallate (TMHCM) cathode (AXM1YM2Z(CN)N.MH2O), where “A” is from a first group of metals, and M1 and M2 are transition metals. The electrolyte includes a first type of cation from the first group of metals, different than “A”. The method connects the cathode and anode to external circuitry to perform initial charge/discharge operations. As a result, a hybrid ion electrolyte is formed including the first type of cation and “A” cations. Subsequently, cations are inserted into the anode during charging, which alternatively may be only “A” cations, only the first type of cation, or both the “A” cations and the first type of cation. Only “A” cations, only the first type, or both “A” and the first type of cation are inserted into the TMHCM during discharge.

Abstract: A mechanism is presented for shielding a cathode in a metal cyanometallate battery. A battery is provided with an anode, a cathode, an electrolyte, and an ion-permeable membrane separating the anode from the cathode. The cathode is made up of a plurality of metal cyanometallate layers overlying the current collector. At least one of the metal cyanometallate layers is an active layer formed from an active material AXM1YM2Z(CN)N·MH2O, where “A” is an alkali metal, alkaline earth metal, or combination thereof. At least one of the metal cyanometallate layers is a shield layer comprising less than 50 percent by weight (wt %) active material. In response to applying an external voltage potential between the cathode and the anode, the method charges the battery. Upon discharge, the shield layer blocks metal particles from contacting active layers. Simultaneously, the shield layer transports metal ions from the electrolyte to the active layers.

Abstract: There are provided an electrolyte-positive electrode structure which comprises a thin solid electrolyte and can develop excellent capacity and output, and a lithium ion secondary battery comprising the same. An electrolyte-positive electrode structure 7 comprises: a positive electrode 4 comprising a positive electrode active material layer 3 formed on a current collector 2; and a solid electrolyte 6 containing inorganic particles having lithium ion conductivity, an organic polymer, and a polymer gel, in which the organic polymer binds the inorganic particles and can be impregnated with the polymer gel, and the polymer gel holds an electrolyte solution and is impregnated into the organic polymer, wherein the positive electrode active material layer 3 is integrated with the solid electrolyte 6 using the organic polymer as a medium.

Abstract: A transition metal hexacyanoferrate (TMH) cathode battery is provided. The battery has a AxMn[Fe(CN)6]y.zH2O cathode, where the A cations are either alkali or alkaline-earth cations, such as sodium or potassium, where x is in the range of 1 to 2, where y is in the range of 0.5 to 1, and where z is in the range of 0 to 3.5. The AxMn[Fe(CN)6]y.zH2O has a rhombohedral crystal structure with Mn2+/3+ and Fe2+/3+ having the same reduction/oxidation potential. The battery also has an electrolyte, and anode made of an A metal, an A composite, or a material that can host A atoms. The battery has a single plateau charging curve, where a single plateau charging curve is defined as a constant charging voltage slope between 15% and 85% battery charge capacity. Fabrication methods are also provided.

Abstract: An electrode binder of a lithium ion battery comprising: (a) a polyvinylidene binder dispersed in an organic diluent with (b) a (meth)acrylic polymer dispersant. The binder can be used in the assembly of electrodes of lithium ion batteries.

Abstract: Iron-sulfide redox flow battery (RFB) systems can be advantageous for energy storage, particularly when the electrolytes have pH values greater than 6. Such systems can exhibit excellent energy conversion efficiency and stability and can utilize low-cost materials that are relatively safer and more environmentally friendly. One example of an iron-sulfide RFB is characterized by a positive electrolyte that comprises Fe(III) and/or Fe(II) in a positive electrolyte supporting solution, a negative electrolyte that comprises S2? and/or S in a negative electrolyte supporting solution, and a membrane, or a separator, that separates the positive electrolyte and electrode from the negative electrolyte and electrode.

Abstract: [Problem] To provide a negative electrode collector for lithium ion secondary batteries, having a high strength and a large discharge capacity. [Means for Resolution] A negative electrode collector using a copper-covered steel foil 10 for carrying a negative electrode active material for lithium ion secondary batteries, which has a steel sheet 6 as the core material thereof and has, on both surfaces thereof, a copper covering layer 7 having a mean thickness tCu of from 0.02 to 5.0 ?m on each surface, and of which the total mean thickness, t, including the copper covering layer 7 is from 3 to 100 ?m with tCu/t of at most 0.3. To the steel sheet 6, for example, applicable is common steel, austenitic stainless steel or ferritic stainless steel. The copper covering layer 7 is, for example, a copper electroplating layer (including one rolled after plating).

Abstract: A nonaqueous secondary battery having a positive electrode having a positive electrode mixture layer, a negative electrode, and a nonaqueous electrolyte, in which the positive electrode contains, as an active material, a lithium-containing transition metal oxide containing a metal element selected from the group consisting of Mg, Ti, Zr, Ge, Nb, Al and Sn, the positive electrode mixture layer has a density of 3.5 g/cm3 or larger, and the nonaqueous electrolyte contains a compound having two or more nitrile groups in the molecule.

Abstract: A method of manufacturing a multicomponent lithium phosphate compound particle with an olivine structure of formula LiyM11-ZM2ZPO4, M1 is Fe, Mn or Co; Y satisfies 0.9?Y?1.2; M2 is Mn, Co, Mg, Ti or Al; and Z satisfies 0<Z?0.1, in which the M2 concentration is continuously lowered from a surface of the particle to a core portion of the particle. The method includes mixing a lithium M1 phosphate compound with an olivine structure of formula LiXM1PO4, M1 is Fe, Mn or Co, and X satisfies 0.9?X?1.2, and a precursor of a lithium M2 phosphate compound with an olivine structure of formula LiXM2PO4, M2 is Mn, Co, Mg, Ti or Al, and X satisfies 0.9?X?1.2, to form a mixture; and subjecting the mixture to heating in an inert atmosphere or a vacuum.

Abstract: Disclosed herein is a highly reliable secondary battery with organic electrolytic solution. The secondary battery has a set of plates for the positive and negative electrodes, with a separator interposed between them, and an organic electrolytic solution composed of an organic solvent and an electrolyte dissolved therein. The organic electrolytic solution contains polyethylene glycol and bis-(3-Sulfopropyl)disulfide.

Abstract: A system for predicting a lifetime of a battery cell, including a learning data input unit, the learning data input unit being configured to receive at least one learning measurement factor and at least one learning factor, a target data input unit, the target data input unit being configured to receive at least one target factor, a machine learning unit, the machine learning unit being coupled to the learning data input unit, the machine learning unit assigning weights to respective ones of the learning factors input to the learning data input unit, and a lifetime prediction unit, the lifetime prediction unit being coupled to the target data input unit and the machine learning unit, the lifetime prediction unit using the weights assigned by the machine learning unit to predict one or more characteristics indicative of the lifetime of the target battery cell.

Abstract: A non-aqueous electrolyte secondary battery has a positive electrode containing a positive electrode active material, a negative electrode, and a non-aqueous electrolyte. The positive electrode active material includes a lithium-containing oxide Lix1Nay1Co?Mn?O?, where 0.66<x1<1.1, 0<y1?0.02, 0.75??<1, 0<??0.25, and 1.9???2.1.

Abstract: A system, method, and articles of manufacture for a surface-modified transition metal cyanide coordination compound (TMCCC) composition, an improved electrode including the composition, and a manufacturing method for the composition. The composition, compound, device, and uses thereof according to AxMn(y-k)Mjk[Mnm(CN)(6-p-q)(NC)p(Che)rq]z.(Che)rw(Vac)(1-z).nH2O (wherein Vac is a Mn(CN)(6-p-q)(NC)p(Che)rq vacancy); wherein Che is an acid chelating agent; wherein: A=Na, K, Li; and M=Mg, Al, Ca, Sc, Ti, V, Cr, Fe, Co, Ni, Cu, Zn, Ga, Pd, Ag, Cd, In, Sn, Pb; and wherein 0<j?4; 0?k?0.1; 0?(p+q)<6; 0<x?4; 0?y?1; 0<z?1; 0<w?0.2; 0<n?6; ?3?r?3; and wherein: x+2(y?k)+jk+(m+(r+1)q?6)z+wr=0.

Abstract: The present invention provides a production method and the like of a microporous stretched film having a high puncture strength and the like. The method includes: a first step of melt-kneading a cellulose nanofiber and a polyolefin resin to thereby disperse the nanofiber in the resin; a second step of removing water from a kneaded mixture obtained in the first step; a third step of mixing a plasticizer in the nanofiber and the resin and melt-kneading them to prepare a polyolefin resin composition; a fourth step of extrusion-molding the polyolefin resin composition; a fifth step of stretching an extrusion-molded article obtained in the fourth step to form a film; and a sixth step of extracting the plasticizer from the film.

Abstract: Disclosed is an additive for a non-aqueous electrolyte, which is a compound having a double bond and at least two cyano groups, the two cyano groups being in a trans-formation to the double bond. Also, a non-aqueous electrolyte comprising the additive and an electrochemical device comprising the non-aqueous electrolyte are also disclosed. Further, an electrode comprising the cyano group-containing compound and an electrochemical device comprising the electrode are disclosed.

Abstract: An electrolyte composition including a macro azo initiator containing a polyethylene oxide repeating unit, and a multi-functional urethane acrylate-based monomer, a gel polymer electrolyte including the electrolyte composition, and a lithium battery including the gel polymer electrolyte.

Abstract: (A) A cathode active material of a cathode includes a lithium phosphate compound represented by LiaM1bPO4 (M is Fe and the like, 0?a?2, b?1). (B) Fine pore distribution of the cathode measured by a mercury intrusion method indicates a peak P1 in a range where a pore diameter is equal to or more than about 0.01 micrometers and less than about 0.15 micrometers, and indicates a peak P2 in a range where the pore diameter is from about 0.15 micrometers to about 0.9 micrometers both inclusive. (C) A ratio I2/I1 between intensity I1 of the peak P1 and intensity I2 of the peak P2 is from about 0.5 to about 20 both inclusive. (D) Porosity of the cathode is from about 30 percent to about 50 percent both inclusive.

Abstract: In an embodiment of the disclosure, a separator utilized in a lithium battery is provided. The separator includes a non-woven polyester support, a porous layer of polyvinylidene fluoride (PVDF) or its derivatives formed on the non-woven polyester support, a layer of UV-curing or thermal-curing polymers formed on top of the porous layer of polyvinylidene fluoride (PVDF) or its derivatives.

Abstract: A protected transition metal hexacyanoferrate (TMHCF) battery cathode is presented, made from AxMyFez(CN)n.mH2O particles, where the A cations are either alkali or alkaline-earth cations, and M is a transition metal. In one aspect the cathode passivation layer may be materials such as oxides, simple salts, carbonaceous materials, or polymers that form a film overlying the AxMyFez(CN)n.mH2O particles. In another aspect, the cathode passivation layer is a material such as oxygen, nitrogen, sulfur, fluorine, chlorine, or iodine that interacts with the AxMyFez(CN)n.mH2O particles, to cure defects in the AxMyFez(CN)n.mH2O crystal lattice structure. Also presented are TMHCF battery synthesis methods.

Abstract: A method and apparatus for manufacturing electrochemical cells. The apparatus and method includes the modification of solid phase material used in electrochemical cells, such as batteries, into a viscous phase for ease of metering and dispensing onto a hot wall reactor to create a substantially uniform cloud of vapor to be deposited on a substrate or other stacks of cells in a continuous or semi-continuous process and having the useful advantage of depositing large volumes of materials for economical manufacturing.

Abstract: Electrochemical devices which incorporate cathode materials that include layered crystalline compounds for which a structural modification has been achieved which increases the diffusion rate of multi-valent ions into and out of the cathode materials. Examples in which the layer spacing of the layered electrode materials is modified to have a specific spacing range such that the spacing is optimal for diffusion of magnesium ions are presented. An electrochemical cell comprised of a positive intercalation electrode, a negative metal electrode, and a separator impregnated with a nonaqueous electrolyte solution containing multi-valent ions and arranged between the positive electrode and the negative electrode active material is described.

Abstract: The invention provides an element including a semiconductor substrate and an electrode disposed on the semiconductor substrate, the electrode being a sintered product of a composition for an electrode that includes phosphorus-containing copper alloy particles, glass particles and a dispersing medium, and the electrode includes a line-shaped electrode having an aspect ratio, which is defined as electrode short length:electrode height, of from 2:1 to 250:1.

Abstract: RFBs having solid hybrid electrodes can address at least the problems of active material consumption, electrode passivation, and metal electrode dendrite growth that can be characteristic of traditional batteries, especially those operating at high current densities. The RFBs each have a first half cell containing a first redox couple dissolved in a solution or contained in a suspension. The solution or suspension can flow from a reservoir to the first half cell. A second half cell contains the solid hybrid electrode, which has a first electrode connected to a second electrode, thereby resulting in an equipotential between the first and second electrodes. The first and second half cells are separated by a separator or membrane.