电解质
锂(药物)
材料科学
阴极
锂钴氧化物
盐(化学)
化学工程
无机化学
氧化物
能量密度
电极
电池(电)
锂离子电池
化学
有机化学
工程物理
物理化学
功率(物理)
医学
物理
量子力学
工程类
冶金
内分泌学
作者
Jinhua Yang,Jiangtao Yu,Xinyu Ma,Xiuyang Zou,Mingchen Yang,Shipeng Sun,Mingzhu Wu,Yin Hu,Feng Yan
标识
DOI:10.1002/aenm.202404107
摘要
Abstract High‐voltage cathodes improve the energy density of the batteries, which satisfies the pursuit of high‐energy‐density lithium metal batteries (LMBs). However, layered lithium cobalt oxide (LiCoO 2 ) cathodes suffer from severe interfacial side reactions under high voltage (4.6 V), which is detrimental for practical applications. Herein, a functional lithium salt, 2,2,6,6‐tetramethyl‐1‐piperidinyloxyl‐4‐sulfate lithium (TEMPO‐OSO 3 Li) is developed that possesses radical‐scavenging anion TEMPO‐OSO 3 − . The anion accumulates at the cathode interface and effectively scavenges free radicals under the electric field at high voltage, thereby, inhibiting the electrolyte decomposition and interfacial side reactions. As a result, the Li||LiCoO 2 batteries with dual‐salt (TEMPO‐OSO 3 Li (0.02 m ) and LiPF 6 (1 m )) electrolyte exhibit high capacity retention of 92% after 100 cycles at 4.6 V and maintain 81% after 200 cycles, which is superior to that of the baseline electrolyte (26%). The work demonstrates a promising strategy for designing electrolyte salts to realize the practical application of LiCoO 2 at high voltage.
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