阳极
煤
碳纤维
钠
化学工程
离子
材料科学
化学
电极
复合材料
有机化学
冶金
物理化学
工程类
复合数
作者
Shengping Hou,Da Zhang,Yong Lei,Yingjie Zhou,Dongrong Yang,Peng Dong,Bowen Xu,Bin Yang,Feng Liang
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-02-07
卷期号:41 (6): 4259-4269
被引量:14
标识
DOI:10.1021/acs.langmuir.4c04935
摘要
Coal-derived hard carbons (CHCs) have considerable potential as sodium storage materials because of their abundant resources and structural diversity. Nevertheless, the smaller layer spacing and ordered carbon microstructure of CHCs bring about low charge/discharge rates and poor cycle life of sodium-ion batteries (SIBs), rendering it challenging to support large-scale energy storage applications. Herein, the preoxidation strategy is employed to achieve multiscale structure optimization of CHCs and improve its sodium storage capacity. The oxygen content in preoxidized coal reached 15.2%, contributing to increasing the cross-linked structure of the coal materials. Particularly, insertion of Na+ is facilitated by large layer spacing of 0.394 nm, as well as the closed pores (0.162 cm3 g-1) improving the diffusion of Na+. Consequently, the rate performance of the as-optimized anode (OCHC3) is superior to that of directly carbonized. Specifically, OCHC3 exhibits a commendable rate performance (201 mAh g-1) and achieves outstanding cycling stability (96.2%) over 500 cycles. Furthermore, galvanostatic intermittent titration reveals the "adsorption-insertion-filling" of OCHC3. This study enlightens the rational design of high-performance HC anodes for SIBs and beyond.
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