A mixed powder for an all-solid-state lithium-ion battery, which is composed of a positive electrode active material for a lithium-ion battery and a solid electrolyte, wherein the positive electrode active material for a lithium-ion battery is composed of particles containing crystals of a lithium metal composite oxide, and the lithium metal composite oxide has a layered structure and contains at least Li and a transition metal, wherein the positive electrode active material for a lithium-ion battery has a particle diameter distribution that satisfies the following Formula (1), and wherein the solid electrolyte has a particle diameter distribution that satisfies the following Formula (2):

[00001]$\left(\text{D90-D10}\right)/\text{D50}\le \text{1}\text{.5}$

[00002]$\left(\text{D90-D10}\right)/\text{D50}\le 2.0$

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

The removal of acid gases (e.g., non-carbon dioxide acid gases) using sorbents that include salts in molten form, and related systems and methods, are generally described.

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

The present disclosure discloses an ABO.sub.3 type high-entropy perovskite Ba.sub.x(FeCoNiZrY).sub.0.2O.sub.3-δ electrocatalytic material and a preparation method thereof, belonging to the technical field of electrocatalytic materials. The electrocatalytic material is prepared by taking hydrated cobalt nitrate, hydrated ferric nitrate, hydrated nickel nitrate, barium nitrate, hydrated yttrium nitrate, hydrated zirconium nitrate and polyacrylonitrile staple fibers as raw materials through processes of liquid phase chelation, gelation, calcination, etc. The prepared high-entropy perovskite Ba.sub.x(FeCoNiZrY).sub.0.2O.sub.3-δ electrocatalytic material can release more electrochemical active sites due to its special nanostructure, thus showing better electrocatalytic activity. Meanwhile, by adjusting the stoichiometric ratio of A/B-site metals, the electronic structure change of five metals in a catalytic center and the change of an oxygen vacancy content are realized, and the purpose of adjusting and optimizing the nitrogen reduction performance is achieved, so that the electrocatalytic material has excellent electrocatalytic conversion of nitrogen gas into ammonia gas.

A nickel hydroxide includes stacked nickel hydroxide layers. Each of the nickel hydroxide layers includes Ni.sup.2+ and OH.sup.−. At least one of the nickel hydroxide layers further includes a type of polyatomic anions. The polyatomic anions include a type of anions that are not SO.sub.4.sup.2− or CO.sub.3.sup.2−.

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

The present invention relates to an electrode material of formula LiFe.sub.1-xCo.sub.xBO.sub.3, where 0<x<1, and to a method of preparing the same comprising independently preparing an iron borate and a cobalt borate and then simultaneously thermally treating them under an inert atmosphere, in the presence of a precursor of lithium and of boric acid.

The present invention relates to an electrode material of formula LiMn.sub.xCo.sub.1-xBO.sub.3, where 0<x<1, and to a method of preparing the same comprising independently preparing a manganese borate and a cobalt borate and then simultaneously thermally treating them under an inert atmosphere, in the presence of a precursor of lithium and of boric acid.

Provided is a positive electrode active material that has high output characteristics and battery capacity when used for a positive electrode of a nonaqueous electrolyte secondary battery and can inhibit gelation of positive electrode mixture paste. A method for producing the positive electrode active material is also provided. A positive electrode active material for a nonaqueous electrolyte secondary battery contains a lithium-nickel-cobalt-manganese composite oxide represented by General Formula (1): Li.sub.i+sNi.sub.xCo.sub.yMn.sub.zB.sub.tM1.sub.uO.sub.2+β and having a hexagonal layered crystal structure. The lithium-nickel-cobalt-manganese composite oxide contains a secondary particle formed of a plurality of flocculated primary particles and a boron compound containing lithium present at least on part of surfaces of the primary particles. A water-soluble Li amount present on the surfaces of the primary particles is up to 0.1% by mass relative to the entire amount of the positive electrode active material.