相间
电解质
阴极
材料科学
锂(药物)
惰性
化学工程
分解
化学物理
电极
化学
物理化学
有机化学
遗传学
医学
生物
工程类
内分泌学
作者
Lianfeng Zou,Peiyuan Gao,Haiping Jia,Xia Cao,Haiping Wu,Hui Wang,Wengao Zhao,Bethany E. Matthews,Zhijie Xu,Xiaolin Li,Ji‐Guang Zhang,Wu Xu,Chongmin Wang
标识
DOI:10.1021/acsami.1c20789
摘要
Solid-electrolyte interphases is essential for stable cycling of rechargeable batteries. The traditional approach for interphase design follows the decomposition of additives prior to the host electrolyte, which, as governed by the thermodynamic rule, however, inherently limits the viable additives. Here we report an alternative approach of using a nonsacrificial additive. This is exemplified by the localized high-concentration electrolytes, where the fluoroethylene carbonate (FEC) plays a nonsacrificial role for modifying the chemistry, structure, and formation mechanism of the cathode-electrolyte interphase (CEI) layers toward enhanced cycling stability. On the basis of ab initio molecular dynamics simulations, we further reveal that the unexpected activation of the otherwise inert species in the interphase formation is due to the FEC-Li+ coordinated environment that altered the electronic states of reactants. The nonsacrificial additive on CEI formation opens up alternative avenues for the interphase design through the use of the commonly overlooked, anodically stable compounds.
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