电解质
溶剂化
材料科学
电化学
阴极
化学工程
电导率
电池(电)
分解
相间
电极
高压
无机化学
电压
离子
化学
有机化学
物理化学
热力学
电气工程
物理
工程类
生物
功率(物理)
遗传学
作者
Xiaoling Cui,Jingjing Zhang,Jie Wang,Peng Wang,Jinlong Sun,Hong Dong,Dongni Zhao,Chunlei Li,Shuxiang Wen,Shiyou Li
标识
DOI:10.1021/acsami.1c19969
摘要
It has been researched that highly concentrated electrolytes (HCEs) can solve the problem of the excessive decomposition of dilute electrolytes at a high voltage, but the mechanism is not clear. In this work, the antioxidation mechanism of HCE at a high voltage was investigated by in situ electrochemical tests and theoretical calculations from the perspective of the solvation structure and physicochemical property. The results indicate that compared with the dilute electrolyte, the change of solvation structures in HCE makes more PF 6 – anions easier to be oxidized prior to the dimethyl carbonate solvents, resulting in a more stable cathode–electrolyte interphase (CEI) film. First, the lower oxidation potential of the solvation structure with more PF 6 – anions inhibits the side effects of the electrolyte effectively. Second, the CEI film, consisted of LiF and Li x PO y F z generated from the oxidation of PF 6 – and Li 3 PO 4 generated from the hydrolysis of LiPF 6 via the soluble PO 2 F 2 – intermediate, can reduce the interface impedance and improve the conductivity. Intriguingly, the high viscosity of HCEs and the hydrolysis of LiPF 6 are proven to play a positive role in enhancing the interfacial stability of the electrolyte/electrode at a high voltage. This study builds a deep understanding of the bulk and interface properties of HCEs and provides theoretical support for their large-scale application in high-voltage battery materials.
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