电解质
阳极
材料科学
分解
相间
化学工程
电化学
石墨
无机化学
半电池
盐(化学)
储能
化学分解
电化学电位
电极
粒子(生态学)
工作(物理)
晶界
纳米颗粒
作者
Zhiyong Wang,Wei Hao,Tong Duan,Shuang Wei,Yuanmao Chen,Tinghu Liu,Jijiang Liu,Yeliang Sheng,Xinyang Yue,Zulipiya Shadike,Zheng Liang
标识
DOI:10.1002/anie.202525822
摘要
ABSTRACT Regulating the electrolyte decomposition to evolve a LiF‐rich solid‐electrolyte interphase (SEI) can reduce the energy barrier of the interfacial Li‐ion transport toward fast‐charging lithium‐ion batteries. Due to the sluggish decomposition kinetics, LiPF 6 , as a widely used Li salt in commercial cells, is unable to build a LiF‐rich SEI. Therefore, expensive fluorinated electrolyte additives are needed. Herein, to eliminate the use of extra fluorinated species, based on the subtle electrochemical decomposition of LiPF 6 occurring ∼2.28 V vs. Li + /Li at 80°C, we developed a temperature‐potential coupled formation (TPCF) protocol, which incorporates a constant‐voltage step (2.28 V) at 80°C to stimulate LiPF 6 decomposition deeply, thereby generating a high‐quality SEI uniformly covering the graphite particle surfaces. This TPCF‐derived SEI is thin and dense, full of LiF grain boundaries, which could reduce the energy barriers of Li + desolvation and interfacial Li + diffusion. Simultaneously, this SEI exhibits a higher work function, effectively suppressing electron leakage to reduce the degeneration of the electrolyte and interphase. Consequently, after a simple TPCF process, the assembled graphite||LiFePO 4 full cell achieves stable cycling at a 6C rate, retaining 80% of its capacity after 3304 cycles and 70.5% after 8940 cycles, outperforming the counterparts.
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