A non-aqueous Li+/Cl− dual-ion battery with layered double hydroxide cathode

被引:0
|
作者
Yuan Q. [1 ]
Wu Y. [1 ]
Dou Y. [1 ,2 ]
Zhang J. [3 ]
Han J. [1 ,2 ]
机构
[1] State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing
[2] Quzhou Institute for Innovation in Resource Chemical Engineering, Zhejiang Province, Quzhou
[3] Ningbo Institute of Materials Technology & Engineering, Chinese Academy of Sciences, Ningbo
关键词
(De)insertion mechanism; Cl[!sup]−[!/sup] storage; Dual-ion batteries; Layered double hydroxide;
D O I
10.1016/j.ces.2024.120357
中图分类号
TM91 [独立电源技术(直接发电)];
学科分类号
摘要
Dual-ion batteries (DIBs) have unique advantages in energy storage, such as high energy density and low cost. However, most studies on organic DIBs use anions with a large ionic radius (PF6−, TFSI−, etc.). Here, we propose a Li+/Cl− dual-ion battery (DIB) through using CoFe-Cl layered double hydroxides (LDHs) and non-aqueous LiCl electrolytes, with a mechanism involving anionic insertion into the LDHs cathode and lithium plating/stripping on the anode. Coupled X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques indicate reversible expansion/extraction of (0 0 3) crystal planes of LDHs and valence state changes of Co and Fe, enabling high Cl− storage capacities of 145 mAh/g and 137 mAh/g at 200 mA/g and 1 A/g, respectively. Furthermore, this DIB demonstrates an impressive power density of 1770 W/kg with an energy density of 240 Wh/kg. This work provides a reference for developing high performance DIBs and expands the electrochemical application field of LDHs. © 2024
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