Solvation structure and solid electrolyte interface engineering for excellent Na+ storage performances of hard carbon with the ether-based electrolytes

电解质 溶剂化 化学工程 乙醚 电化学 无定形碳 碳纤维 无定形固体 溶剂 材料科学 化学 无机化学 有机化学 物理化学 电极 复合数 工程类 复合材料
作者
Zhiqiang Lv,Tianyu Li,Xin Hou,Canpei Wang,Huamin Zhang,Jingwang Yan,Qiong Zheng,Xianfeng Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:430: 133143-133143 被引量:73
标识
DOI:10.1016/j.cej.2021.133143
摘要

Compared with the commonly used ester-based electrolytes, more excellent Na+ storage performances can be achieved for hard carbon in the ether-based electrolyte. Whereas, the mysteries underlying such excellent electrochemical performances are still unclear. Herein, the impressive Na+ storage behaviors of hard carbon in the ether-based electrolyte were clarified based on a profound insight of Na+ storage mechanism. It’s revealed that the co-intercalation behavior is responsible for the lower de-solvation energy, which contributes to a facile de-solvation process and the enhanced charge transfer kinetic. Besides, a thin, amorphous and flexible solid-electrolyte interface (SEI) in ether-based electrolyte with a specific structure where the amorphous nanoparticles are coated with organic species was probed. And the resulted SEI is beneficial to achieving much lower activation energy for Na+ diffusion through SEI and a stable interface during cycling due to its excellent ion-conducting ability and mechanical flexibility. It’s also demonstrated that ether-based solvent with short chain length plays a positively impact on the Na+ storages, which also well agrees with the above synergistic effect. The research plays a significant role in elucidating the uniqueness of ether-based electrolytes to hard carbon and promoting its practical application in future sodium-based battery chemistries.
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