相间
材料科学
电解质
化学工程
碳酸乙烯酯
磷酸盐
锂(药物)
化学稳定性
动力学
阴极
聚合
共价键
催化作用
单体
碳酸盐
无机化学
溶解
六氟磷酸盐
工作(物理)
作者
Hengyu Ren,Xiaohu Wang,Wenwei Cai,W H Zhao,Kunchen Xie,Dongwen Zou,Tao Zeng,Funing Yu,Zhikang Deng,Haocong Yi,Chunyu Xu,Wenhua Zhang,Shunning Li,Qinghe Zhao,Feng Pan
摘要
ABSTRACT The stable interfacial chemistry of LiCoO 2 (LCO) is the cornerstone for its high‐voltage operation. However, interfacial side reactions, originating from the Co/O catalytic sites, lead to ethylene carbonate (EC) oxidation, lithium hexafluorophosphate (LiPF 6 ) hydrolysis, and LCO surface degradation. Herein, we propose that the formation of functional phosphate derivatives (FPD) in the electrolyte, which are generated from the reaction between tris(trimethylsilyl) phosphate (TMSP) and PF 6 − anions, can achieve targeted regulation of the polyphosphates cathode‐electrolyte interphase (CEI). During cycling, the FPD spontaneously forms covalent interactions with surface Co/O sites, triggering in situ polymerization that constructs a robust and full‐coverage CEI on LCO. The resulting CEI is enriched with polyphosphates and LiF/Li 2 O, which ensures high thermodynamic stability and fast Li + transport kinetics simultaneously. Consequently, the LCO with optimized electrolyte (1.0 M LiPF 6 in fluoroethylene carbonate (FEC)‐based solvents with 2.0 wt.% TMSP) demonstrates exceptional cell performance with a high capacity retention of 81.0% after 3000 cycles within 3.0–4.6 V (vs. Li/Li + ), 81.6% after 2000 cycles within 3.0–4.65 V, and shows the feasibility in the LCO||graphite pouch cell with a retention of 80.0% after 500 cycles. This work provides a new insight into the uniform CEI construction for high‐voltage LCO cathodes through functional electrolyte engineering.
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