材料科学
阴极
电解质
锂(药物)
锂钴氧化物
电化学
阳极
表面改性
分析化学(期刊)
快离子导体
化学工程
离子电导率
氧化钴
离子
氧化物
锂离子电池
电池(电)
电极
化学
物理化学
热力学
有机化学
冶金
医学
功率(物理)
色谱法
内分泌学
工程类
物理
作者
Xiaolei Zhang,Bo Peng,Liping Zhao,Guanglin Wan,Feng Wang,Suyuan Zeng,Hongli Zhang,Jinwen Ding,Genqiang Zhang
标识
DOI:10.1021/acsami.2c00533
摘要
Lithium cobalt oxide (LCO) as a classic layered oxide cathode for lithium-ion batteries is limited by the cutoff voltage, which only delivers about half of the theoretical capacity (∼4.2 V, 140 mA h g-1). Recently, raising the cutoff voltage to 4.6 V has been considered to further improve its specific capacity. However, LCO suffers from serious phase transition of O3 to H1-3, which leads to dramatic volume change and loss of cobalt, finally resulting in rapid capacity decay. In this work, we introduce the NASICON-structured LiZr2(PO4)3 (LZP), an ion conductor for lithium ion, to modify the surface of LCO by a wet-chemical method. Such a surface modification improves lithium-ion diffusion between the interface of LCO and electrolyte and restrains the O3 to H1-3 phase transition. As a result, the optimized LCO with 1 wt % coating (denoted as LCO@LZP-1%) demonstrates enhanced electrochemical performance in both half-cell and full-cell. To be specific, LCO@LZP-1% delivers a high specific capacity of 161.3 mA h g-1 and increases the capacity retention from 37.8 to 75.1% within 100 cycles. Importantly, the full-cell assembled by LCO@LZP-1% and artificial graphite can exhibit an outstanding energy density of 345.5 W h kg-1 (based on the total mass of cathode and anode).
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