Insights into Anion‐Solvent Interactions to Boost Stable Operation of Ether‐Based Electrolytes in Pure‐SiOx||LiNi0.8Mn0.1Co0.1O2 Full Cells

电解质 溶剂 材料科学 乙醚 离子 无机化学 化学 有机化学 电极 物理化学
作者
Yifan Tian,Shuang‐Jie Tan,Zhuo‐Ya Lu,Di‐Xin Xu,Hanxian Chen,Chaohui Zhang,Xusheng Zhang,Ge Li,Yuming Zhao,Wan‐Ping Chen,Quan Xu,Rui Wen,Juan Zhang,Yu‐Guo Guo
出处
期刊:Angewandte Chemie [Wiley]
卷期号:62 (33) 被引量:37
标识
DOI:10.1002/anie.202305988
摘要

Ether solvents with superior reductive stability promise excellent interphasial stability with high-capacity anodes while the limited oxidative resistance hinders their high-voltage operation. Extending the intrinsic electrochemical stability of ether-based electrolytes to construct stable-cycling high-energy-density lithium-ion batteries is challenging but rewarding. Herein, the anion-solvent interactions were concerned as the key point to optimize the anodic stability of the ether-based electrolytes and an optimized interphase was realized on both pure-SiOx anodes and LiNi0.8 Mn0.1 Co0.1 O2 cathodes. Specifically, the small-anion-size LiNO3 and tetrahydrofuran with high dipole moment to dielectric constant ratio realized strengthened anion-solvent interactions, which enhance the oxidative stability of the electrolyte. The designed ether-based electrolyte enabled a stable cycling performance over 500 cycles in pure-SiOx ||LiNi0.8 Mn0.1 Co0.1 O2 full cell, demonstrating its superior practical prospects. This work provides new insight into the design of new electrolytes for emerging high-energy density lithium-ion batteries through the regulation of interactions between species in electrolytes.
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