Boosting high initial coulombic efficiency of hard carbon by in-situ electrochemical presodiation

被引:32
作者
Qin, Nannan [1 ]
Sun, Yanyan [1 ,4 ]
Hu, Chao [1 ]
Liu, Sainan [2 ]
Luo, Zhigao [3 ]
Cao, Xinxin [1 ,4 ]
Liang, Shuquan [1 ,4 ]
Fang, Guozhao [1 ,4 ]
机构
[1] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410083, Hunan, Peoples R China
[3] Xiangtan Univ, Coll Chem, Xiangtan 411105, Hunan, Peoples R China
[4] Cent South Univ, Key Lab Elect Packaging & Adv Funct Mat Hunan Prov, Changsha 410083, Hunan, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2023年 / 77卷
基金
中国国家自然科学基金;
关键词
Hard carbon; In situ presodiation; Initial coulombic efficiency; Solid electrolyte interface; Sodium-ion batteries;
D O I
10.1016/j.jechem.2022.10.032
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hard carbon (HC) is a promising anode material for sodium ion batteries (SIBs), whereas inferior initial coulombic efficiency (ICE) severely limits its practical application. In the present work, we propose an in situ electrochemical presodiation approach to improve ICE by mixing sodium biphenyl (Na-Bp) dimethoxyethane (DME) solution with DME-based ether electrolyte. A solid electrolyte interface (SEI) could be formed beforehand on the HC electrode and Na+ was absorbed to nanopores and graphene stacks, compensating for the sodium loss and preventing electrolyte decomposition during the initial charge and discharge cycle. By this way, the ICE of half-cells was increased to nearly 100 % and that of full-cells from 45% to 96% with energy density from 132.9 to 230.5 W h kg-1. Our work provides an effi-cient and facile method for improving ICE, which can potentially promote the practical application of HC-based materials.(c) 2022 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:310 / 316
页数:7
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