材料科学
电解质
阴极
离域电子
锂(药物)
电池(电)
氧化物
金属
金属锂
储能
荷电状态
锂离子电池
化学工程
磷酸钒锂电池
离子
化学物理
过渡金属
纳米技术
电荷(物理)
无机化学
电化学
锂电池
作者
Jianwei Wang,Kai He,Shuangjiang Li,Zipeng Sun,Zhipeng Yin,Kaijie Miao,Yaoxin Li,chengwei ma,Jiangqi Zhou
标识
DOI:10.1002/adfm.202531823
摘要
ABSTRACT Lithium metal batteries are considered the most promising candidates for next‐generation energy storage devices due to their high‐energy density. To unleash the potential of lithium metal batteries, they are typically paired with oxide cathodes that can operate at high voltages. However, under high‐voltage conditions, the structural collapse of oxide cathodes and the crossover effect of transition metal ions not only cause damage to the cathode structure, but also impair the interface stability of lithium metal anodes. Herein, a design strategy for charge delocalization effect solvents was proposed in this work, which breaks through the limitations of traditional performance optimization strategies for high‐voltage lithium metal batteries. This charge delocalization electrolyte system can effectively construct a fast dynamic interface. The Li||NCM811 battery assembled with this electrolyte system exhibits 72.64% (N/p = 1.5) capacity retention after 400 cycles at a high‐voltage of 4.6 V, which is a high level in high‐voltage electrolytes. Even with a high mass loading of 18.4 mg cm −2 , the battery also reaches capacity retention of 86.33% after 70 cycles. This research result lays the foundation for the development of high‐voltage lithium metal batteries.
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