C01G45/12

Lithiated transition metal oxides

Process for the fabrication of an electrode structure comprising an electrochemically active material suitable for use in an energy storage device. The method includes electrodepositing the electrochemically active material onto an electrode in electrodeposition bath containing a non-aqueous electrolyte. The electrode structure can be used for various applications such as electrochemical energy storage devices including high power and high-energy lithium-ion batteries.

Lithium battery electrodes

Electrode materials for electrochemical cells and batteries and methods of producing such materials are disclosed herein. The electrode materials comprise an active lithium metal oxide material prepared by: (a) contacting the lithium metal oxide material with an aqueous acidic solution containing one or more metal cations; and (b) heating the so-contacted lithium metal oxide from step (a) to dryness at a temperature below 200° C. The metal cations in the aqueous acidic solution comprise one or more metal cations selected from the group consisting of an alkaline earth metal ion, a transition metal ion, and a main group metal ion.

Catalyst for organic substance decomposition and organic substance decomposing apparatus

A catalyst for decomposing an organic substance, the catalyst having a body which has a plurality of pores and the body contains a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where the A contains at least one selected from Ba and Sr, the B contains Zr, the M is at least one selected from Mn, Co, Ni, and Fe, 1.001≤x≤1.1, 0.05≤z≤0.2, y+z=1, and w is a positive value that satisfies electrical neutrality. The average pore diameter of the plurality of pores is 49 nm to 260 nm and the pore volume of each of the plurality of pores is 0.08 cm.sup.3/g to 0.37 cm.sup.3/g.

METHOD FOR PREPARING CATHODE ACTIVE MATERIAL
20220220003 · 2022-07-14 ·

The inventive concept discloses a method for preparing a cathode active material containing a lithium manganese oxide exhibiting a reversible phase transition, and exhibiting electrochemical characteristics of the lithium manganese oxide through the reversible phase transition including (A) synthesizing a sodium manganese oxide using a manganese precursor, and (B) reacting the sodium manganese oxide with a lithium precursor to synthesize the lithium manganese oxide, or including (C) directly synthesizing the lithium manganese oxide.

Mixed oxide and its use as NOx adsorber

The present disclosure is directed to a mixed oxide composition comprising manganese, aluminum and/or magnesium, and a rare earth element; a method of making the mixed oxide composition; a NOx adsorber comprising the mixed oxide composition; an exhaust system for internal combustion engines comprising the NOx adsorber; and a method for reducing NOx in an exhaust gas that employs the NOx adsorber.

Mixed oxide and its use as NOx adsorber

The present disclosure is directed to a mixed oxide composition comprising manganese, aluminum and/or magnesium, and a rare earth element; a method of making the mixed oxide composition; a NOx adsorber comprising the mixed oxide composition; an exhaust system for internal combustion engines comprising the NOx adsorber; and a method for reducing NOx in an exhaust gas that employs the NOx adsorber.

NICKEL COBALT COMPLEX HYDROXIDE PARTICLES AND METHOD FOR PRODUCING THE SAME, POSITIVE ELECTRODE ACTIVE MATERIAL FOR NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY AND METHOD FOR PRODUCING THE SAME, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY

A method for producing a nickel cobalt complex hydroxide includes first crystallization of supplying a solution containing Ni, Co and Mn, a complex ion forming agent and a basic solution separately and simultaneously to one reaction vessel to obtain nickel cobalt complex hydroxide particles, and a second crystallization of, after the first crystallization, further supplying a solution containing nickel, cobalt, and manganese, a solution of a complex ion forming agent, a basic solution, and a solution containing said element M separately and simultaneously to the reaction vessel to crystallize a complex hydroxide particles containing nickel, cobalt, manganese and said element M on the nickel cobalt complex hydroxide particles crystallizing a complex hydroxide particles comprising Ni, Co, Mn and the element M on the nickel cobalt complex hydroxide particles.

Miniature battery with constant electrode pressure and electrolyte reservoir

An electrochemical voltage source has an anode containing lithium, a cathode containing manganese oxide, and a housing. The cathode and the anode are arranged in an interior of the housing and are arranged opposite one another. An electrolyte reservoir in the form of a compressible storage body, which receives an electrolyte, is arranged between the anode and the cathode. The storage body has a first side resting against an end face of the cathode and a second side, which faces away from the first side, and rests against an end face of the anode. The cathode experiences an increase in volume when the voltage source is discharged. The anode experiences a decrease in volume during the discharge. During the discharge, the absolute value of the volume increase of the cathode is at least as great as the absolute value of the volume decrease of the anode.

SOLID ELECTROLYTE, ELECTROLYTE LAYER AND BATTERY

A solid electrolyte having high electrical conductivity even in a low-temperature region is provided. A solid electrolyte containing a hexagonal perovskite-related compound, in which the compound is a compound represented by the following general formula (1), and an electrolyte layer and a battery using the solid electrolyte are disclosed. Ba.sub.7-αNb.sub.(4−x-y)Mo.sub.(1+x)M.sub.yO.sub.(20+z) (1), in the formula (1), M is a cation of at least one element; a represents a Ba deficiency amount and represents a value of 0 or more and 0.5 or less, x represents a value of −1.1 or more and 1.1 or less, y represents a value of 0 or more and 1.1 or less, and z represents an oxygen non-stoichiometry and represents a value of −2.0 or more and 2.0 or less, provided that in the formula (1), |x|+y≥0.01 is satisfied.

Lithium transition metal oxide particles having lithium concentration gradients, methods for forming the same, and battery cathodes formed of the same
11279628 · 2022-03-22 · ·

Previous hybrid-anion and cation-redox (HACR) cathodes were limited in cycling performance by irreversible anionic redox reactions caused by the loss of anions. To overcome this limitation, a lithium (Li) transition metal (M) oxide particle is described having a Li concentration gradient. In one example, the particle includes a Li-rich core region that provides capacity and energy density due anionic and cationic contributions and a Li-poor surface region surrounding the core region to inhibit anionic activity and thus substantially reduce the loss of anions. A gradient region disposed between the core and surface regions has a Li concentration profile that varies from a first Li concentration in the core region to a second Li concentration in the surface region. A high-temperature leaching method may be used to leach LiO from a Li-rich Li.sub.1+xM.sub.1−XO.sub.2 particle, thus forming a coherent Li gradient with a stabilized layered structure.