Hybrid covalent organic-framework-based electrolytes for optimizing interface resistance in solid-state lithium-ion batteries

被引:24
作者
Cheng, Dongming [1 ]
Sun, Cui [2 ]
Lang, Zhongling [1 ]
Zhang, Jinhua [2 ]
Hu, Ajuan [2 ]
Duan, Jianing [2 ]
Chen, Xinyu [1 ]
Zang, Hong-Ying [1 ]
Chen, Jiajia [2 ]
Zheng, Mingsen [2 ]
Dong, Quanfeng [2 ]
机构
[1] Northeast Normal Univ, Key Lab Polyoxometalate & Reticular Mat Chem, Fac Chem, Minist Educ Univ Jilin Prov, Changchun 130024, Jilin, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat iChEM, State Key Lab Phys Chem Solid Surfaces,Dept Chem, Xiamen 361005, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYMER ELECTROLYTES; CONDUCTIVITY; MEMBRANE; STORAGE; ENERGY; LI+;
D O I
10.1016/j.xcrp.2021.100731
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High ion conductivity and low electrode-electrolyte interface resistance are intensively pursued topics for the development of solidstate Li-ion batteries with high safety and energy density. Here, we propose a design using keto-enamine covalent organic frameworks (TPBD) and polyethylene oxide (PEO) to prepare a solid-state electrolyte (TPBD-LiPF6@PEO), achieving a high ion conductivity of 0.543 mS cm(-1) at 25 degrees C and optimizing the electrode-electrolyte interface resistance in Li-ion batteries. Solid-state nuclear magnetic resonance experiments and density functional theory calculations show that the strong interaction between the -C=O site in TPBD and Li+ ions promotes the dissociation of LiPF6. The assembled LiFePO4 vertical bar TPBD-LiPF6@PEO vertical bar Li batteries without using liquid electrolytes offer a specific capacity of nearly 140 mAh g(-1) at 0.2 C with a columbic efficiency of 99.6% after 200 cycles at 25 degrees C. This strategy for preparing solid-state electrolytes provides practical ideas and suggestions in the development of solid-state energy devices.
引用
收藏
页数:13
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