Hon Hai Precision Industry Co., Ltd.

Tsinghua University

Ding-Sheng Wang

Ya-Dong Li

Jun Lu

Qing Peng

Wei Chen

Feng Bai

Zi-Yang Huo

Li-Ping Liu

Xiao-Ling Xiao

Wei-Yang Wang

Xiang-Wen Liu

A cathode composite material includes a cathode active material and a coating layer coated on a surface of the cathode active material. The cathode active material includes a layered type lithium transition metal oxide. A material of the coating layer is a lithium metal oxide having a crystal structure belonging to C2/c space group of the monoclinic crystal system. The present disclosure also relates to a lithium ion battery including the cathode composite material.

Cathode composite material and lithium ion battery using the same

A cathode composite material includes a cathode active material and a coating layer coated on a surface of the cathode active material. The cathode active material includes a layered type lithium nickel cobalt manganese oxide. The coating layer comprises a lithium metal oxide having a crystal structure belonging to C2/c space group of the monoclinic crystal system. The present disclosure also relates to a lithium ion battery including the cathode composite material.

A cathode composite material includes a cathode active material and a coating layer coated on a surface of the cathode active material. The cathode active material includes a lithium cobalt oxide. The coating layer includes a lithium metal oxide having a crystal structure belonging to C2/c space group of the monoclinic crystal system. The present disclosure also relates to a lithium ion battery including the cathode composite material.

A method for preparing a cathode active material of lithium battery is shown. The method includes providing MnOOH and lithium source material, and mixing the MnOOH and the lithium source material in a liquid solvent to achieve a mixture. Then, the mixture is dried to remove the liquid solvent, thereby achieving a precursor. A temperature of the precursor is elevated from room temperature to a sintering temperature of about 500&#xb0; C. to about 900&#xb0; C. at a uniform rate, and the precursor is sintered at the sintering temperature for about 3 hours to about 24 hours.

Method for preparing cathode active material of lithium battery

A method for making the mesoporous material includes the following steps: dissolving a nanocrystal powder in an organic solvent, and achieving a solution A with concentration of 1-30 mg/ml; dissolving a surfactant in water, and achieving a solution B with an approximate concentration of 0.002-0.05 mol/ml; mixing the solution A and the solution B in a volume ratio of 1:(5-30), and achieving a mixture; stirring and emulsifying the mixture, until an emulsion C is achieved; removing the organic solvent from the emulsion C, and achieving a deposit; washing the deposit with deionized water, and achieving a colloid; and drying and calcining the colloid, and eventually achieving a mesoporous material. The mesoporous material has a large specific surface area, a high porosity, and a narrow diameter distribution.

Method for making mesoporous material

A method for making the metal oxide includes the following steps: mixing a metal nitrate with a solvent of octadecyl amine, and achieving a mixture; agitating and reacting the mixture at a reaction temperature for a reaction period; cooling the mixture to a cooling temperature, and achieving a deposit; and washing the deposit with an organic solvent, drying the deposit at a drying temperature and achieving a metal oxide nanocrystal. The present method for making a metal oxide nanocrystal is economical and timesaving, and has a low toxicity associated therewith. Thus, the method is suitable for industrial mass production. The metal oxide nanocrystal material made by the present method has a readily controllable size, a narrow size distribution, and good crystallinity.

Method for making metal oxide nanocrystal

A method for making colloidal nanocrystals includes the following steps: dissolving a nanocrystal powder in an organic solvent, and achieving a solution A of a concentration of 1-30 mg/ml; dissolving a surfactant in water, and achieving a solution B of a concentration of 0.002-0.05 mmol/ml; mixing the solution A and the solution B in a volume ratio of 1: (5-30), and achieving a mixture; stirring and emulsifying the mixture, until an emulsion C is achieved; removing the organic solvent from the emulsion C, and achieving a deposit; then washing the deposit with deionized water, and achieving colloidal nanocrystals. The present method for making colloidal nanocrystals is economical and timesaving, and has a low toxicity associated therewith. Thus, the method is suitable for industrial mass production. The colloidal nanocrystals made by the present method have a readily controllable size, a narrow size distribution, and good configuration.

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Beijing, China

Ding-Sheng Wang