电解质
电化学
溶剂化
钠
分解
动力学
化学
化学工程
盐(化学)
阴极
电池(电)
无机化学
离子
电极
材料科学
有机化学
物理化学
热力学
工程类
物理
功率(物理)
量子力学
作者
Fangyuan Cheng,Meilian Cao,Qing Li,Chun Fang,Jiantao Han,Yunhui Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-09-14
卷期号:17 (18): 18608-18615
被引量:175
标识
DOI:10.1021/acsnano.3c07474
摘要
NaClO 4 and NaPF 6, the most universally adopted electrolyte salts in commercial sodium-ion batteries (SIBs), have a decisive influence on the interfacial chemistry, which is closely related to electrochemical performance. The complicated and ambiguous interior mechanism of microscopic interfacial chemistry has prevented reaching a consensus regarding the most suitable sodium salt for high-performance SIB electrolytes. Herein, we reveal that the solvation structure induced by different sodium salt anions determines the Na + desolvation kinetics and interfacial film evolution process. Specifically, the weak interaction between Na + and PF 6 – promoted sodium desolvation and storage kinetics. The solvation structure involving PF 6 – induced the anion’s preferential decomposition, generating a thin, inorganic compound–rich cathode–electrolyte interphase that ensured interface stability and inhibited solvent decomposition, thereby guaranteeing electrode stability and promoting the charge transfer kinetics. This study provides clear evidence that NaPF 6 is not only more compatible with industrial processes but also more conducive to battery performance. Commercial electrolyte design employing NaPF 6 will undoubtedly promote the industrialization of SIBs.
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