电解质
碳酸盐
阴极
电化学
拉曼光谱
化学工程
氧化剂
材料科学
无机化学
再分配(选举)
氧化物
碳酸二甲酯
相间
金属
碳酸锂
电极
化学
电化学电池
电化学电位
金属锂
极化(电化学)
锂(药物)
碳酸丙烯酯
限制
过渡金属
电极电位
作者
Qi Yu,Kaixiang Ren,Xinchun Song,Kepeng Bao,Zihan Xu,Zhipeng Jiang,Yongtao Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-08-03
卷期号:26 (31): 10489-10497
标识
DOI:10.1021/acs.nanolett.6c02687
摘要
Carbonate additives such as vinylene carbonate (VC) and fluoroethylene carbonate (FEC) are widely used to stabilize high-voltage lithium metal batteries (LMBs), but their roles are generally interpreted through a static film-forming mechanism. Here, we reassess their functions at LiNi0.8Co0.1Mn0.1O2 (NCM811) cathodes up to 4.6 V using in-situ electrochemical surface-enhanced Raman spectroscopy (EC-SERS), theoretical calculations, and systematic electrochemical evaluation. VC and FEC not only contribute to cathode electrolyte interphase formation but also dynamically regulate the cathode-side electric double layer (EDL). By reducing its potential sensitivity, they suppress potential-driven redistribution and excessive enrichment of carbonate solvents and PF6- near the highly oxidizing NCM811 surface, thereby limiting continuous electrolyte decomposition. Compared with VC, FEC provides more durable protection by forming a LiF-rich organic-inorganic hybrid interphase. These findings reveal a new EDL-regulation mechanism for conventional carbonate additives and are expected to provide guidance for electrolyte design in high-voltage LMBs.
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