Abstract: This application provides a negative electrode plate, including an active layer 1 and an active layer 2. The active layer 1 contains an active material 1, and the active layer 2 contains an active material 2. A powder OI value of the active material 1 falls in a range of 8 to 32, and a powder OI value of the active material 2 falls in a range of 2 to 7. A gram capacity of the active material 1 falls in a range of 290 to 350 mAh/g, and a gram capacity of the active material 2 falls in a range of 350 to 368 mAh/g. A ratio ? of the powder OI value between the active material 1 and the active material 2 falls in a range of 2.00 to 6.25.

Abstract: In an embodiment, a Li-ion battery electrode comprises a conductive interlayer arranged between a current collector and an electrode active material layer. The conductive interlayer comprises first conductive additives and a first polymer binder, and the electrode active material layer comprises a plurality of active material particles mixed with a second polymer binder (which may be the same as or different from the first polymer binder) and second conductive additives (which may be the same as or different from the first conductive additives). In a further embodiment, the Li-ion battery electrode may be fabricated via application of successive slurry formulations onto the current collector, with the resultant product then being calendared (or densified).

Abstract: A secondary battery includes a positive electrode, a negative electrode, and an electrolytic solution. The positive electrode includes a lithium-cobalt composite oxide having a layered rock-salt crystal structure. The negative electrode includes graphite. A potential variation of the positive electrode is greater than or equal to 2 mV when the secondary battery is discharged from a full charge state by a capacity corresponding to 1% of a maximum discharge capacity. The maximum discharge capacity is a discharge capacity obtained when the secondary battery is discharged with a constant current from the full charge state until the closed circuit voltage reaches 3.00 V, following which the secondary battery is discharged with a constant voltage of the closed circuit voltage of 3.00 V for 24 hours.

Abstract: A positive electrode active material for a secondary battery is provided, which includes a lithium composite transition metal oxide including nickel (Ni), cobalt (Co), and manganese (Mn), wherein a particle of the lithium composite transition metal oxide includes a core portion and a resistance portion formed on a surface of the core portion, and is composed of a single particle, wherein the core portion has a layered crystal structure of space group R-3m, and the resistance portion has a cubic rock-salt structure of space group Fm-3m.

Abstract: Provided is a lithium secondary battery which includes a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and an electrolyte, wherein the positive electrode includes, as a positive electrode active material, a lithium composite transition metal oxide powder having a layered structure and a nickel content accounting for 50 atm % to 75 atm % of total transition metals, and wherein the lithium composite transition metal oxide powder undergoes a 3% or less change in lithium-oxygen (Li—O) interlayer spacing (i.e., LiO6 slab thickness) in a state-of-charge (SOC) range of 58% to 86%.

Abstract: A capacitor and methods of processing an anode metal foil are presented. The capacitor includes a housing, one or more anodes disposed within the housing, one or more cathodes disposed within the housing, one or more separators disposed between an adjacent anode and cathode, and an electrolyte disposed around the one or more anodes, one or more cathodes, and one or more separators within the housing. The one or more anodes each include a metal foil that includes a first plurality of tunnels through a thickness of the metal foil in a first ordered arrangement, the first ordered arrangement being a close packed hexagonal array arrangement, and having a first diameter, and a second plurality of tunnels through the thickness of the metal foil having a second ordered arrangement and a second diameter greater than the first diameter.

Abstract: A negative electrode for a lithium secondary battery including a negative electrode current collector; and a negative electrode active material layer formed on the negative electrode current collector, wherein the negative electrode active material layer includes graphite and silicon oxide, and lithium is incorporated in the negative electrode active material layer, and a method for preparing the same.

Abstract: A main object of the present disclosure is to provide a method for producing an electrode of which uncoated part can stretch while inhibiting breakage.

Abstract: Aspects of the disclosure relate to electrode active composites for use in battery cells that include a cathode active material including oxygen and an oxygen scavenging oxide. The cathode active material can be a blend of a lithium metal phosphate and an over-lithiated oxide. Advantageously, the blend of a lithium metal phosphate and over-lithiated oxide can have a higher energy density relative to the lithium metal phosphate alone and the oxygen scavenging oxide can improve the stability of the active composite.

Abstract: The invention relates to a method for the precipitation of a solid material, where the method comprises: providing an aqueous metal ion solution, said metal ion solution comprising TiOSO4 and metal ions of a metal M, where M is one or more of the elements: Mg, Co, Cu, Ni, Mn, Fe; providing an aqueous carbonate solution; and mixing said aqueous metal ion solution and said aqueous carbonate solution thereby providing a solid material comprising titanium and a metal carbonate comprising said metal(s) M, where the titanium is homogeneously distributed within the solid material. The invention also relates to a solid material, a method of preparing a positive electrode material for a secondary battery from the solid material and the use of the solid material as a precursor for the preparation of a positive electrode material for a secondary battery.

Abstract: This application provides a lithium-ion battery, a positive electrode plate for a lithium-ion battery, and an apparatus. The lithium-ion battery includes a positive electrode plate that includes a positive current collector and a positive active material layer arranged on at least one surface of the positive current collector. A positive active material in the positive active material layer includes a positive active substance I and a positive active substance II. The positive active substance I is a layered lithium nickel transition metal oxide. The positive active substance II is an olivine-type li-containing phosphate. The positive electrode plate satisfies 2.5?N/(PD×(1?P1)×(1?A))?21. The positive electrode plate for a lithium-ion battery has relatively high energy density, and a high transmission rate of lithium ions, which effectively increases instantaneous discharge power under a low SOC while ensuring high volume energy density of lithium-ion batteries using the positive electrode plate.

Abstract: A battery 2 includes an outer can 10 and an electrode group 22 that is housed in the outer can 10 together with an alkaline electrolytic solution, in which a positive electrode 24 included in the electrode group 22 includes a positive electrode substrate and a positive electrode mixture supported on the positive electrode substrate, the positive electrode mixture includes nickel hydroxide, yttrium oxide serving as a first additive, and niobium oxide or titanium oxide serving as a second additive, a total amount of the first additive and the second additive is 0.1 parts by mass or more and 2.5 parts by mass or less per 100 parts by mass of the nickel hydroxide, a mass ratio of the first additive and the second additive is in a relationship of 1:0.2 to 5, and the positive electrode mixture after an activation treatment has a resistivity of 1 ?·m or more and 10 ?·m or less.

Abstract: A main object is to provide a method of producing a cathode active material having a high average discharge potential, and a high degree of stability at high potential. A step of preparing a Na-doped precursor of making a transition metal oxide having a P2 structure belonging to a space group of P63/mmc; and an ion exchange step of substituting lithium for at least part of sodium contained in the transition metal oxide by an ion exchange method are included, wherein the transition metal oxide has the composition represented by NaaMnx?pNiy?qCoz?rM1p+q+rO2, where 0.5?a?1, x+y+z=1, 3?4x+2y+3z?3.5, and 0.05?p+q+r<0.25, M1 is Al or Mo, when M1 is Al, p is not equal to q, and any one of p and q is not 0.

Abstract: To provide a cathode active material capable of reducing cathode resistance of a secondary battery by enhancing electron conductivity thereof without reducing discharge capacity of the secondary battery. Lanthanum compound particles each having a perovskite-type structure are dispersed on surfaces of secondary particles of a lithium transition metal-containing composite oxide and/or in gaps or grain boundaries between primary particles thereof. The lanthanum compound particles have a cross-sectional average particle size of 0.70 ?m or less. The number of lanthanum compound particles present per unit area of the cross sections of the secondary particles is 0.03 particles/?m2 to 0.10 particles/?m2, and the number of lanthanum compound particles present per unit area of the surfaces of the secondary particles is 0.01 particles/?m2 to 0.25 particles/?m2. The content of lanthanum with respect to the entire cathode active material is within a range of 0.1% by mass to 5% by mass.

Abstract: This application relates to an electrode active composition, a preparation method thereof, an electrode, a battery, and an apparatus. The electrode active composition includes: a first component, the first component being lithium cobalt oxide particles; and a second component, the second component being ternary material particles. The first component includes lithium cobalt oxide particles with a particle size greater than 11 ?m and lithium cobalt oxide particles with a particle size less than 6 ?m, and a ratio in number of the lithium cobalt oxide particles with a particle size greater than 11 ?m to the lithium cobalt oxide particles with a particle size less than 6 ?m is 0.2-4.8, and in some embodiments, 0.2-2.8. A summed number of the lithium cobalt oxide particles with a particle size greater than 11 ?m and the lithium cobalt oxide particles with a particle size less than 6 ?m accounts for above 90% of a total number of particles in the first component.

Abstract: A main object of the present disclosure is to provide an anode material that is used in a fluoride ion battery and can prevent the decrease in operating voltage while inhibiting occurrence of short circuit. The present disclosure achieves the object by providing an anode material to be used in a fluoride ion battery, the anode material comprising a Mg material containing a Mg element, and a fluoride ion conductive material containing at least one kind of metal element excluding a Mg element, and a F element.

Abstract: A method for preparing a positive electrode active material precursor includes preparing a metal aqueous solution including a nickel raw material, a cobalt raw material, and a manganese raw material (step 1); adding the metal aqueous solution, an ammonium cation complex forming agent, and a basic aqueous solution into a reactor, co-precipitating the mixture at pH 11 to less than pH 12 to form nuclei of first positive electrode active material precursor particles and growing the nuclei (step 2); adjusting input amount of the basic aqueous solution to increase the pH in the reactor to a range of 0.8 to 1.5 compared to that of step 2; and adjusting input amount of the basic aqueous solution to change the pH in the reactor to pH 11 to less than pH 12 (step 4). A positive electrode active material precursor prepared by the above preparation method has an improved packing density.

Abstract: A method for producing a high-nickel positive electrode active material, a positive electrode active material produced thereby, and a positive electrode and a lithium secondary battery including the same is provided. The method includes preparing a lithium composite transition metal oxide having a nickel content of 80 atm % or greater among transition metals, washing the lithium composite transition metal oxide, and mixing the washed lithium composite transition metal oxide with an aluminum raw material and heat treating the mixture at a temperature of 650° C. to 690° C. to obtain a positive electrode active material having a surface portion doped with aluminum.

Abstract: The present invention relates to a positive electrode active material for a lithium secondary battery and a lithium secondary battery including the same. The positive electrode active material according to the present invention reduces the specific surface area and grain boundary of a secondary particle in which a side reaction with an electrolyte solution occurs to improve the high-temperature stability of the positive electrode active material and reduce gas generation caused by the positive electrode active material.

Abstract: An electrode component for an electrochemical cell is provided herein. The electrode component includes a current collector having a first surface, a metal oxide layer disposed on the first surface of the current collector, and a lithium-containing layer bonded to the first surface of the current collector. The metal oxide layer includes a plurality of features. A method for manufacturing such an electrode component is also provided herein. The method includes directing a laser beam toward the first surface of the current collector in the presence of oxygen to form the metal oxide layer on the first surface and applying the lithium-containing layer to the metal oxide layer thereby bonding the lithium-containing layer with the current collector.

Abstract: A lithium secondary battery includes a cathode formed from a cathode active material including a cathode active material particle having a specific concentration ratio, an anode; and a separation layer interposed between the cathode and the anode. The lithium secondary battery has improved formation discharge amount, formation discharge efficiency and power output.

Abstract: A sodium ion secondary battery includes a cyclic organic compound as an active material and a complex hydride as a solid electrolyte, wherein the cyclic organic compound has at least two carbonyl groups —C(?O)—, the at least two carbonyl groups are bonded via a single bond or at least one conjugated double bond, and the complex hydride includes a Na cation and a complex ion containing H.

Abstract: Configurations for an interferometric device used for multiplexing and de-multiplexing light are disclosed. The interferometric device may include a first input waveguide, a second input waveguide, an interferometric waveguide, and an output waveguide. A fundamental mode of light may be launched into the first and second input waveguides, and the interferometric waveguide may receive the fundamental mode and generate a higher order mode of light, where the two modes of light may be superimposed while propagating through the interferometric waveguide. The two modes of light may be received at an output waveguide that collapses the two modes into a single mode. The light propagating through the interferometric device may be used for increasing optical power even though the wavelengths of light may be different from one another. Additionally, the interferometric device may reduce coherent noise.

Abstract: A method of manufacturing a cathode active material for a lithium secondary battery according to embodiments of the present invention includes performing a first heat treatment on a first mixture of a transition metal precursor and a lithium precursor at a first calcination temperature to obtain a preliminary lithium-transition metal composite oxide particle; and performing a second heat treatment on a second mixture obtained by adding the lithium precursor to the preliminary lithium-transition metal composite oxide particle at a second calcination temperature which is lower than the first calcination temperature to form a lithium-transition metal composite oxide particle.

Abstract: The present invention provides a composite oxide that can achieve a high low-temperature output characteristic, a method for manufacturing the same, and a positive electrode active material in which the generation of soluble lithium is suppressed and a problem of gelation is not caused during the paste preparation. A positive electrode active material for non-aqueous electrolyte secondary batteries, including a lithium-metal composite oxide powder including a secondary particle configured by aggregating primary particles containing lithium, nickel, manganese, and cobalt, or a lithium-metal composite oxide powder including both the primary particles and the secondary particle, wherein the secondary particle has a hollow structure inside as a main inside structure, the slurry pH is 11.5 or less, the soluble lithium content rate is 0.5 [% by mass] or less, the specific surface area is 2.0 to 3.0 [m2/g], and the porosity is 20 to 50 [%].

Abstract: A nonaqueous electrolyte for a lithium ion battery includes a lithium salt, a first nonaqueous solvent, and an additive mixture comprising a first operative additive of lithium difluorophosphate and a second operative additive of either fluoro ethylene carbonate or vinylene carbonate. A lithium-ion battery includes a negative electrode, a positive electrode comprising NMC with micrometer-scale grains, a nonaqueous electrolyte having lithium ions dissolved in a first nonaqueous solvent, and an additive mixture having a first operative additive of either fluoro ethylene carbonate or vinylene carbonate and a second operative additive of either 1,3,2-dioxathiolane-2,2-dioxide, another sulfur-containing additive, or lithium difluorophosphate.

Abstract: Disclosed herein are electrolytes and electrochemical devices. The electrochemical devices comprise cathodes that include nickel-rich layered lithium transition metal oxides, lithium-rich layered transition-metal oxides, lithium manganese-based spinel oxides, lithium polyanion-based compounds, and combinations thereof. The electrolytes include a lithium imide salt, an aprotic acyclic carbonate solvent, and an additive, wherein the additive comprises a metal salt, an aprotic solvent, or a combination thereof. The electrolyte can be stable at a voltage of 4.3 V or above vs. Li/Li+.

Abstract: Embodiments described in this application relate generally to a system, an apparatus and/or methods for manufacturing electrodes by infusion electrolyte into compacted electrode materials. In some embodiments, a working electrode materials can be produced using an infusion mixing and manufacturing process. In some embodiments, a single-sided finished electrode can be produced directly from a dry powder mixture using an infusion mixing and manufacturing process. In some embodiments, a double-sided finished electrode can be produced directly from a dry powder mixture using an infusion mixing and manufacturing process. The electrodes produced by an infusion mixing and manufacturing process generally perform better than those produced by non-infusion processes.

Abstract: The application relates to a positive active material precursor including a transition metal composite oxide precursor. The transition metal composite oxide precursor exhibits a peak full width at half maximum of a (200) plane (2?=about 42° to about 44°) in X-ray diffraction analysis in a range of about 0.3° to about 0.5°. The application also relates to a positive active material using the precursor, a method of preparing the same, and a positive electrode and a rechargeable lithium battery including the same.

Abstract: A charging method of a non-aqueous electrolyte secondary battery involves a first charging step in which, defining x as the ratio of the capacity of a silicon compound to the rated capacity Q (0.1?x?0.5), charging is performed at a first fixed current value I1st that satisfies the expression below; and a high current charging step in which after completion of the first charging step, charging is performed at a fixed current value Imax higher than the first fixed current value I1st.

Abstract: A positive electrode active material in which a capacity decrease caused by charge and discharge cycles is suppressed is provided. Alternatively, a positive electrode active material having a crystal structure that is unlikely to be broken by repeated charging and discharging is provided. The positive electrode active material contains titanium, nickel, aluminum, magnesium, and fluorine, and includes a region where titanium is unevenly distributed, a region where nickel is unevenly distributed, and a region where magnesium is unevenly distributed in a projection on its surface. Aluminum is preferably unevenly distributed in a surface portion, not in the projection, of the positive electrode active material.

Abstract: A more efficient and lower cost method for producing electrochemically stable, and thus safe from thermal runaway, high electrochemical capacity coated lithium nickelate is disclosed. The coated nickelate hydroxide particles are formed from a mixed metal sulfate solution (MMS) serving as the starting material that is obtained from recycled lithium ion and/or nickel metal hydride batteries. The coating of the particles includes a relatively small amount of cobalt/manganese oxide forming the surface of the nickelate particles, while the core of the particles includes a relatively large amount of nickel in relation to the weight of the coating. Battery cathode electrodes may be manufactured by using the obtained coated lithium nickelate particles as the cathode active material (CAM) in forming the battery cathodes.

Abstract: The present disclosure relates to an anode for a lithium secondary battery, wherein an anode material layer is formed on at least one surface of an anode current collector, and the anode material layer includes large-particle graphite, a small-particle silicon-based material, and fine-particle graphite, and satisfies the following conditions 1 to 3: [Condition 1] Average diameter D50 of the large-particle graphite (D1): 1 to 50 ?m [Condition 2] Average diameter D50 of the small-particle silicon-based material (D2): 0.155D1 to 0.414D1 [Condition 3] Average diameter D50 of the fine-particle graphite (D3): 0.155D1 to 0.414D1, or 0.155D2 to 0.414D2.

Abstract: An electrode catalyst for an Oxygen Reduction Reaction (ORR) is provided that includes a transition metal nitride layer on a substrate, an ORR surface oxide layer deposited on the transition metal nitride layer, where the ORR surface oxide layer includes from sub-monolayer to 20 surface oxide monolayers.

Abstract: A lithium manganate positive electrode active material, comprising a lithium manganate matrix and a cladding layer as a “barrier layer” and a “functional layer” are described. The cladding layer can not only “prevent” the transition metal ions which have been produced by the lithium manganate matrix from directly “running” into the electrolyte solution, but also “prevent” the hydrofluoric acid in the electrolyte solution from directly contacting with the lithium manganate substrate, and then prevent the lithium manganate matrix from dissolving out more transition metal manganese ions; as a “functional layer”, the cladding layer contains various effective ingredients inside, which can reduce the transition metal manganese ions already present inside the battery through chemical reactions or adsorption effects, thus slowing down the generation of transition metal manganese and the decomposition of the SEI film (solid electrolyte interphase film) catalyzed by the transition metal manganese.

Abstract: A positive electrode active material according to the present disclosure includes a lithium composite oxide that contains first particles having a crystal structure belonging to space group R-3m and second particles having a crystal structure belonging to space group C2/m. The crystal structure of the second particles has a larger amount of cation mixing than the crystal structure of the first particles. The second particles have a smaller particle size than the first particles. Mathematical Formula 0.05?integrated intensity ratio I(18°-20°)/I(43°-46°)?0.99 is satisfied. The integrated intensity ratio I(18°-20°)/I(43°-46°) is a ratio of the integrated intensity I(18°-20°) to the integrated intensity I(43°-46°). The integrated intensity I(A°-B°) is the integrated intensity of a maximum peak present in the range of angle of diffraction 2? greater than or equal to A° and less than or equal to B° in the X-ray diffraction pattern of the lithium composite oxide.

Abstract: A charging method of a non-aqueous electrolyte secondary battery involves a first charging step in which, defining x as the ratio of the capacity of a silicon compound to the rated capacity Q (0.1?x?0.5), charging is performed at a first fixed current value I1st that satisfies the expression below; and a high current charging step in which after completion of the first charging step, charging is performed at a fixed current value Imax higher than the first fixed current value I1st.

Abstract: In some embodiments, an electrode can include a current collector, a composite material in electrical communication with the current collector, and at least one phase configured to adhere the composite material to the current collector. The current collector can include one or more layers of metal, and the composite material can include electrochemically active material. The at least one phase can include a compound of the metal and the electrochemically active material. In some embodiments, a composite material can include electrochemically active material. The composite material can also include at least one phase configured to bind electrochemically active particles of the electrochemically active material together. The at least one phase can include a compound of metal and the electrochemically active material.

Abstract: A lithium-ion secondary battery includes a positive electrode, a negative electrode, and an electrolytic solution. The electrolytic solution includes a solvent, an electrolyte salt, and an aminoanthraquinone polymer compound. The aminoanthraquinone polymer compound includes a divalent maleic anhydride part and a divalent aminoanthraquinone derivative part.

Abstract: A positive electrode active material for a secondary battery which includes a nickel-based lithium composite transition metal oxide including nickel (Ni), wherein the lithium composite transition metal oxide satisfies Equation 1 and Equation 2 below 80 nm?crystallite sizeFWHM?150 nm??[Equation 1] ?size(|crystallite sizeIB?crystallite sizeFWHM|)?20??[Equation 2] wherein, in Equation 1 and Equation 2, crystallite sizeFWHM is a crystallite size obtained by calculating from X-ray diffraction (XRD) data using a full width at half maximum (FWHM) method, and crystallite sizeIB is a crystallite size obtained by calculating from XRD data using an integral breadth (IB) method.

Abstract: In some embodiments, an electrode can include a first and second conductive layer. At least one of the first and second conductive layers can include porosity configured to allow electrolyte to flow therethrough. The electrode can also include an electrochemically active layer having electrochemically active material sandwiched between the first and second conductive layers. The electrochemically active layer can be in electrical communication with the first and second conductive layers.

Abstract: The invention is directed towards a battery. The battery includes a cathode, an anode, a separator between the cathode and the anode, and an electrolyte. The cathode includes a conductive additive and an electrochemically active cathode material. The electrochemically active cathode material includes a beta-delithiated layered nickel oxide. The beta-delithiated layered nickel oxide has a chemical formula. The chemical formula is LixAyNi1+a?zMzO2·nH2O where x is from about 0.02 to about 0.20; y is from about 0.03 to about 0.20; a is from about 0 to about 0.2; z is from about 0 to about 0.2; and n is from about 0 to about 1. Within the chemical formula, A is an alkali metal. The alkali metal includes potassium, rubidium, cesium, and any combination thereof. Within the chemical formula, M comprises an alkaline earth metal, a transition metal, a non-transition metal, and any combination thereof. The anode includes an electrochemically active anode material.

Abstract: A battery module, a battery pack, and an electric apparatus are provided. In some embodiments, the battery module includes a first type of cell and a second type of cell that are cells of different chemical systems, where the first type of cell includes n first cells, the second type of cell includes m second cells, n and m each are selected from an integer greater than 1, at least one of the first cells and at least one of the second cells are electrically connected in series, and the first cell and the second cell satisfy at least the following relationships: 0.08??RB/?RA?3.50, and 0.10 m?/100 cycles??RA?0.40 m?/100 cycles, where ?RA is a discharge resistance growth rate of the first cell, and ?RB is a discharge resistance growth rate of the second cell; and IMPB<IMPA, where IMPA is an alternating current impedance of the first cell, and IMPB is an alternating current impedance of the second cell.

Abstract: Provided are a cathode active material for a lithium secondary battery, a method for preparing the same, and a lithium secondary battery comprising the same. The cathode active material for a lithium secondary battery comprises: a lithium metal compound; and a lithium compound disposed on the surface of the lithium metal compound, wherein the content of lithium contained in the lithium compound is 0.25 parts by weight or less with respect to 100 parts by weight of the lithium metal compound, wherein the specific surface area of the lithium compound is between 0.5 m2/g and 2.0 m2/g, and the pH of the lithium compound is between 11.5 and 12.3.

Abstract: Disclosed are a secondary battery, an active material, a method for preparing the same, and a lithium secondary battery including the same. In an embodiment, provided is a secondary battery including a positive electrode, a negative electrode and an electrolyte, wherein the secondary battery further includes a reaction-inducing substance located in any one of the positive electrode, the negative electrode and the electrolyte, wherein the reaction-inducing substance forms a reaction product by consuming thermal energy when exposed to a predetermined temperature or higher in a use environment of the secondary battery, thereby improving thermal safety of the secondary battery.

Abstract: A method of producing a rechargeable lithium battery cell, the method comprising (a) preparing a liquid electrolyte solution comprising an ion-conducting polymer dispersed in a first liquid solvent and an optional lithium salt dissolved in the first liquid solvent; (b) impregnating the electrolyte solution into the cathode, the anode, a porous structure of the separator, or the battery cell; (c) removing the first liquid solvent; and (d) impregnating a second liquid solvent, comprising an optional lithium salt dissolved therein, into the cathode, the anode, the separator porous structure, or the battery cell; wherein the ion-conducting polymer comprises a polymer having an ion conductivity from 10?8 S/cm to 10?2 S/cm when measured at room temperature without the presence of a liquid solvent and the polymer does not occupy more than 25% by weight of the cathode, not counting a current collector weight.

Abstract: Provided are electrochemical cells, comprising water-retaining components, and methods of fabricating such electrochemical cells. A water-retaining component is configured to deliver water to the positive active material during the operation of the electrochemical cell. The water-retaining component may be a part of the positive active material layer, a part of the electrolyte layer, and/or a standalone component. In some examples, the water-retaining component comprises one or more crystal hydrates (e.g., MgSO4, MgCl2, Na2SO4, Na2HPO4, CuSO4, CaCl2, KAl(SO4)2, and Mg(NO3)2), one or more water-retaining polymers (e.g., sodium polyacrylate, potassium polyacrylate, ammonium polyacrylate, and a cellulose derivative), one or more inorganic compounds (e.g., fumed silica, precipitated silica). In some examples, a method of forming an electrochemical cell comprises printing a positive active material layer, a negative active material layer, and an electrolyte layer, e.g.

Abstract: Provided is an organic sulfur material comprising a sulfur-modified acrylic resin, wherein an acrylic resin is at least one polymer selected from the group consisting of (a) a polymer of at least one selected from the group consisting of acrylate compounds represented by CH2?C(R11)COOR12, wherein R11 is a hydrogen atom or a methyl group and R12 is an alkyl group, and (b) a polymer of at least one selected from the group consisting of acrylate compounds above and at least one selected from the group consisting of diacrylate compounds represented by CH2?C(R21)COO—Y—OCO(R22)C?CH2, wherein each of R21 and R22 is the same or different and is a methyl group, etc., Y is a hydrocarbylene group, etc., wherein the hydrocarbylene group may have a substituent selected from a hydroxyl group and an alkyl group.

Abstract: A method for preparing a positive electrode active material for a secondary battery is provided. The method includes preparing a lithium composite transition metal oxide including nickel, cobalt, and manganese (Mn), wherein the content of the nickel in the total content of the transition metal is 60 mol % or greater. The lithium composite transition metal oxide, MgF2 as a fluorine (F) coating source, and a boron (B) coating source undergoes dry mixing and heat treatment to form a coating portion on the particle surface of the lithium composite transition metal oxide. In addition, a positive electrode active material prepared as described above, is also provided.

Abstract: A process for making a cathode active material for a lithium ion battery is described. The process includes (a) a step of synthesizing a mixed oxide of formula Li1+xTM1?xO2 at a temperature ranging from 750 to 1000° C. in an oxidizing atmosphere, where TM is a combination of two or more transition metals of Mn, Co and Ni and, optionally, at least one more metal of Ba, Al, Ti, Zr, W, Fe, Cr, K, Mo, Nb, Mg, Na and V, and x is a number ranging from zero to 0.2, (b) a step of cooling down the material obtained from step (a) to a temperature ranging from 100 to 400° C., (c) a step of adding at least one reactant of BF3, SO2 and SO3 at the temperature of 100 to 400° C., and (d) a step of cooling down to a temperature of 50° C. or below.