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Positive electrode material of lithium-ion battery and preparation method therefor

專利號
US11996560B1
公開日期
2024-05-28
申請人
Beijing Easpring Material Technology Co., Ltd.(CN Beijing)
發(fā)明人
Junfan Tong; Yanbin Chen; Yuqiang Jin; Wenbo Wang; Xuequan Zhang; Yafei Liu
IPC分類
H01M4/00; C01G53/00; H01M4/131; H01M4/505; H01M4/525; H01M10/0525
技術(shù)領(lǐng)域
calcining,electrode,positive,manganese,cobalt,dopant,material,nickel,lithium,in
地域: Beijing

摘要

The present disclosure relates to a positive electrode material for a lithium ion battery and its preparation. The positive electrode material in accordance with the present disclosure has an intrinsic specific surface area of 5-13 m2/g. The positive electrode material in accordance with the present disclosure has an intrinsic specific surface area and an intrinsic pore size within the required ranges. In this regard, the positive electrode material in accordance with the present disclosure has excellent particle strength, excellent Li ion transference ability, and good resistance to electrolyte erosion. When used in lithium batteries, it may impart the batteries with excellent rate performance and cycle performance. The present disclosure also relates to a method for preparing the positive electrode material.

說明書

In one embodiment, a coating layer is provided on at least part of the surface of the second calcined product. The coating layer may comprise at least one oxide selected from a group consisting of B2O3, Al2O3, SiO2 and W2O5. The providing of the coating layer may comprise mixing the second calcined product with a coating agent, and subjecting to a third calcining at 250-500° C. In providing of the coating layer, the mixing may be operated by ball milling, shearing, grinding, blending and the like. The second calcined product and the coating agent are mixed in a molar ratio of, for example, 1:0.01-0.1. Preferably, the mixing may be operated for 1-4 hours. The coating agent may be a material that can be converted into the coating layer under the conditions of the third calcining. It may include, for example, boric acid, aluminum hydroxide, pseudo boehmite, boehmite, gibbsite, bayerite, silicic acid, orthosilicic acid or ammonium paratungstate.

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