There is provided a lithium-transition metal oxide powder with a coating layer containing lithium niobate formed on a part or the whole part of a surface of a lithium-transition metal oxide particle and having a low powder compact resistance, and a positive electrode active material for a lithium ion battery containing the lithium-transition metal oxide powder. Specifically, there is provided the lithium-transition metal oxide powder composed of a lithium-transition metal oxide particle with a part or the whole part of a surface coated with a coating layer containing lithium niobate, wherein a carbon-content is 0.03 mass % or less.

The present disclosure relates to a cathode active material, and more particularly, to a cathode active material doped with a trivalent metal (Me) and a lithium secondary battery comprising the same. According to one aspect, there is provided the cathode active material doped with the trivalent metal (Me), represented by the formula Li.sub.xMn.sub.2Me.sub.yO.sub.4 (here, x is from 0.5 to 1.3, and y is from 0.01 to 0.1). According to the present disclosure, release of manganese ions of the cathode active material greatly reduces, and consequently, capacity and cycle life of the battery may be significantly improved.

Process for manufacturing a lithiated transition metal oxide, said process comprising the steps of (a) mixing at least one lithium salt and a precursor selected from transition metal oxides, transition metal oxyhydroxides, transition metal hydroxides, and transition metal carbonates, (b) pre-calcining the mixture obtained in step (a) at a temperature in the range of from 300 to 700° C., and (c) calcining the pre-calcined mixture according to step (b) in a multi-stage fluidized bed reactor at a temperature in the range of from 550° C. to 950° C., wherein the temperatures in step (b) and (c) are selected in a way that step (c) is being performed at a temperature higher than that of step (b).

A producing method of a solution that contains lithium, at least one of a niobium complex and a titanium complex, and ammonia, wherein an amount of the ammonia in the solution is 0.3 mass % or less. The solution is suitable for forming a coating layer capable of improving battery characteristics of an active material in a battery.

Described herein is a method for producing ferrite nanocrystals. The method includes providing a solution including a fatty acid, an aliphatic amine and an alcoholic solvent, adding at least one organometallic precursor compound including a metal selected from the group consisting of Fe, Mn, Co and Zn and an aromatic organic molecule to the solution thereby obtaining a reaction mixture, transferring the reaction mixture to a sealed reactor, thereby obtaining a filling percentage of the sealed reactor between 20 and 70 vol. %, and heating the sealed reactor to a temperature between 160° C. and 240° C. for at least 3 hours.

A lithium-ion secondary battery having high capacity and excellent charge and discharge cycle performance is provided. A secondary battery having high capacity is provided. A secondary battery having excellent charge and discharge performance is provided. A secondary battery in which a decrease in capacity is suppressed even at high temperatures is provided. The secondary battery includes a positive electrode, a negative electrode, an electrolyte solution, and an exterior body. The positive electrode includes a positive electrode active material. The positive electrode active material contains lithium, cobalt, oxygen, magnesium, and fluorine. The number of magnesium atoms contained in the positive electrode active material is greater than or equal to 0.001 times and less than or equal to 0.1 times the number of cobalt atoms contained in the positive electrode active material. The positive electrode active material includes a region having a layered rock-salt crystal structure. The electrolyte solution contains an ionic liquid. The exterior body includes a metal layer and a polymer layer stacked over the metal layer. The polymer layer includes a region in contact with the electrolyte solution.

Supplemental lithium can be used to stabilize lithium ion batteries with lithium rich metal oxides as the positive electrode active material. Dramatic improvements in the specific capacity at long cycling have been obtained. The supplemental lithium can be provided with the negative electrode, or alternatively as a sacrificial material that is subsequently driven into the negative electrode active material. The supplemental lithium can be provided to the negative electrode active material prior to assembly of the battery using electrochemical deposition. The positive electrode active materials can comprise a layered-layered structure comprising manganese as well as nickel and/or cobalt.

Provided is a lithium secondary battery having both visible light transparency and flexibility. A lithium secondary battery includes: a positive electrode film formed on a flexible transparent film substrate and capable of intercalating and deintercalating lithium ions; a transparent electrolyte having lithium ion conductivity; and a negative electrode film formed on a flexible transparent film substrate, the negative electrode film being a metal capable of forming an alloy with lithium or capable of intercalating and deintercalating lithium ions. When the positive electrode film contains a lithium source, the negative electrode film is made to have a thickness of 50 nm to 300 nm by using, as a negative electrode material, any of tin oxide, silicon oxide, titanium oxide, tungsten oxide, niobium oxide, molybdenum oxide, metal phosphide, metal sulfide, metal nitride, metal fluoride, or metal titanium composite oxide.

Provided is a method for inhibiting extractant degradation in the DSX process through the manganese extraction control, the method comprising: (a) stirring DSX solvent and DSX feed solution, which is a solution containing a valuable metal from which iron has been removed in an agitator, in which soda ash (Na.sub.2CO.sub.3) is further added to maintain a constant pH; and (b) scrubbing the manganese from the DSX solvent, extracted in step (a).

The present invention refers to material comprising a compound of the formula ABOx wherein x is >1.5 and ≤2.5, A is independently selected from a transition metal of IUPAC groups 10 and 11, and B is independently selected from a transition metal of IUPAC group 6, 7, 8 or 9 or a main group element of IUPAC group 13, as highly active catalyst for hydrogen evolution reaction (HER).