Use of aluminum in a lithium rich cathode material of the general formula (I) for suppressing gas evolution from the cathode material during a charge cycle and for increasing the charge capacity of the cathode material.

The disclosure discloses a method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material. The waste lithium cobaltate cathode material is calcined, and then measured; a lithium source, a magnesium source, nano-scale TiO.sub.2 and the waste lithium cobaltate cathode material powder are mixed to obtain a mixture, placed in a ball milling tank containing absolute ethanol, and the resulting mixture is ball milled, and then dried to obtain a mixed powder; the mixed powder is calcined to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material; the magnesium-titanium co-doped regenerated lithium cobaltate cathode material is added into a mixed solution obtained by ultrasonically mixing absolute ethanol with the aluminum source, and then heated and stirred continually until the solvent evaporates to obtain a residue; the residue is calcined to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

The present application discloses a positive electrode active material including a lithium nickel cobalt manganese oxide, the molar content of nickel in the lithium nickel cobalt manganese oxide accounts for 60%-90% of the total molar content of nickel, cobalt and manganese, and the lithium nickel cobalt manganese oxide has a layered crystal structure of a space group R 3m; a transition metal layer of the lithium nickel cobalt manganese oxide includes a doping element, and the local mass concentration of the doping element in particles of the positive electrode active material has a relative deviation of 20% or less; and in a differential scanning calorimetry spectrum of the positive electrode active material in a 78% delithiation state, an initial exothermic temperature of a main exothermic peak is 200° C. or more, and an integral area of the main exothermic peak is 100 J/g or less.

A ceramic powder for a ceramic component, in particular based on zirconia and/or alumina, in particular for a timepiece or jewelry piece. The powder includes at least one noble metal among platinum, rhodium, osmium, palladium, ruthenium and iridium, at a quantity of less than or equal to 5% by weight.

A positive electrode active material includes a lithium transition metal oxide represented by Formula 1, and a lithium-containing inorganic compound layer formed on a surface of the lithium transition metal oxide,
Li.sub.1+a(Ni.sub.bCo.sub.cX.sub.dM.sup.1.sub.eM.sup.2.sub.f).sub.1−aO.sub.2  [Formula 1] in Formula 1, X is at least one selected from the group consisting of manganese (Mn) and aluminum (Al), M.sup.1 is at least one selected from the group consisting of sulfur (S), fluorine (F), phosphorus (P), and nitrogen (N), M.sup.2 is at least one selected from the group consisting of zirconium (Zr), boron (B), cobalt (Co), tungsten (W), magnesium (Mg), cerium (Ce), tantalum (Ta), titanium (Ti), strontium (Sr), barium (Ba), hafnium (Hf), F, P, S, lanthanum (La), and yttrium (Y), 0≤a≤0.1, 0.6≤b≤0.99, 0≤c≤0.2, 0≤d≤0.2, 0<e≤0.1, and 0<f≤0.1. A method of preparing the positive electrode active material, a positive electrode and a lithium secondary battery are also provided.

Disclosed herein are materials and processes for production of lithium oxide materials, such as lithium lanthanum zirconium oxide (LLZO), having a small particle size and high density for use in lithium-ion batteries. Some embodiments are directed to forming and then heating a multiphase material comprising lithium carbonate and La.sub.2Zr.sub.2O.sub.7 in the presence of hydrogen gas at a temperature below the melting point of the lithium carbonate, such that at least a portion of the lithium carbonate decomposes to form lithium oxide. In some embodiments, the lithium oxide is heated to a temperature sufficient to crystallize the lithium oxide to form the solid electrolyte material comprising lithium lanthanum zirconium oxide (LLZO) particles.

A process to produce graphene dual doped with nitrogen and sulfur atoms through a reduction of graphene oxide by microorganisms. Also, graphene dual doped with nitrogen and sulfur atoms obtainable by this process, and the use of the doped graphene to produce e.g. electronic components or water purification equipment. The process is eco-sustainable and economic with the additional advantage of providing a product with significantly improved performance compared to known products.

Provided are a sodium ion-conductive crystal-containing solid electrolyte sheet capable of giving excellent battery characteristics even when reduced in thickness, and an all-solid-state battery using the same. The solid electrolyte sheet contains at least one type of sodium ion-conductive crystal selected from β″-alumina and NASICON crystal and has a thickness of 500 μm or less and a flatness of 200 μm or less.

The present disclosure is related to a method for applying a functional compound on sulfur particles by means of an atmospheric pressure plasma discharge including a gas or an activated gas flow resulting from the atmospheric pressure plasma discharge. The coating composition includes an inorganic electrically conductive compound, an electrically conductive carbon compound, an organic precursor compound of a conjugated polymer, a precursor of a hybrid organic-inorganic compound, or a mixture, and the functional compound provides the sulfur particles with an electrically conductive surface.

A process for producing a surface-modified particulate lithium nickel metal oxide material is provided. The process comprises the addition of a controlled quantity of a coating liquid comprising a metal-containing compound and a lithium-containing compound to nickel metal precursor particles using an incipient wetness process followed by a calcination step.