材料科学
电解质
相间
阴极
扩散
相(物质)
电压
涂层
烧结
高压
离子
锂(药物)
活化能
化学工程
电极
分析化学(期刊)
复合材料
电气工程
有机化学
热力学
物理化学
工程类
色谱法
生物
内分泌学
遗传学
医学
量子力学
物理
化学
作者
Wen Zhang,Meng Wang,Miao Chang,Fangyuan Cheng,Yuyu Li,Shixiong Sun,Yue Xu,Liang Wang,Leimin Xu,Qing Li,Chun Fang,Yuhao Lu,Jiantao Han
标识
DOI:10.1016/j.ensm.2024.103446
摘要
The advancement of high charging cut-off voltage stands as a crucial avenue to enhance the energy density of LiCoO2 (LCO). However, LCO faces severe interface and bulk phase issues at high voltage (≥ 4.6 V), resulting in poor cycling stability. In this study, we reconstruct the surface structure of LCO based on the interdiffusion reaction between LCO and MgF2 in a high-temperature sintering process. Specifically, this interdiffusion reaction yields an ultra-thin LiF coating layer, artificially reinforcing the chemical structure of the cathode-electrolyte interphase (CEI) during cycling. This LiF-rich CEI not only effectively protects the surface structure of LCO, but also facilitates the lithium-ion diffusion. Furthermore, the diffusion of F and Mg into the LCO lattice significantly strengthens the structure, which inhibits unfavorable phase transitions from the O3 phase to the H1-3 phase at high voltage. Consequently, such modified LCO with concurrently enhanced interface and bulk structure exhibits outstanding long-term cycling performance within 3.0–4.6 V at 1 C, achieving a capacity retention of 84.9% after 1000 cycles. Meanwhile, it also demonstrates excellent high-temperature performance, with a capacity retention of 85.0% after 200 cycles under 45 °C.
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