成核
电解质
结晶
电化学
相间
材料科学
化学工程
化学
阳极
相(物质)
等温过程
离子
热力学
化学物理
物理化学
电极
有机化学
物理
生物
工程类
遗传学
作者
Chong Yan,Lili Jiang,Yuxing Yao,Yang Lu,Jia‐Qi Huang,Qiang Zhang
标识
DOI:10.1002/anie.202100494
摘要
Solid electrolyte interphase (SEI) has been widely employed to describe the new phase formed between anode and electrolyte in working batteries. Significant advances have been achieved on the structure and composition of SEI as well as on the possible ion transport mechanism. However, the nucleation and growth mechanism of SEI catches little attention, which requires the establishment of isothermal electrochemical crystallization theory. Herein we explore the virgin territory of electrochemically crystallized SEI. By using potentiostatic method to regulate the decomposition of anions, an anion-derived SEI forms on graphite surface at atomic scale. After fitting the cur-rent-time transients with Laviron theory and Avrami formula, we conclude that the formation of anion-derived interface is surface reaction controlled and obeys the two-dimensional (2D) progressive nucleation and growth model. Atomic force microscope (AFM) images emphasize the conclusion, which reveals the mystery of isothermal electrochemical crystallization of SEI.
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