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
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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