High?Performance Na?Ion Storage of S?Doped Porous Carbon Derived from Conjugated Microporous Polymers

被引:6
|
作者
Yuquan Li [1 ]
Bin Ni [1 ]
Xiaodan Li [2 ]
Xianghui Wang [1 ]
Dafeng Zhang [3 ]
Qingfei Zhao [4 ]
Jinliang Li [2 ]
Ting Lu [1 ,5 ]
Wenjie Mai [2 ]
Likun Pan [1 ]
机构
[1] Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University
[2] Siyuan Laboratory, Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials, Department of Physics, Jinan University
[3] School of Materials Science and Engineering, Liaocheng University
[4] Testing and Analysis Centre, College of Chemistry and Materials Science, Shanghai Normal University
[5] Department of Chemical Engineering, School of Environmental and Chemical Engineering, Shanghai University
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Conjugated microporous polymer; S-doped porous carbons; Na-ion batteries; Reaction mechanism;
D O I
暂无
中图分类号
TM912 [蓄电池]; TQ127.11 [];
学科分类号
0808 ; 0817 ;
摘要
Na-ion batteries(NIBs) have attracted considerable attention in recent years owing to the high abundance and low cost of Na. It is well known that S doping can improve the electrochemical performance of carbon materials for NIBs. However, the current methods for S doping in carbons normally involve toxic precursors or rigorous conditions. In this work, we report a creative and facile strategy for preparing S-doped porous carbons(SCs) via the pyrolysis of conjugated microporous polymers(CMPs). Briefly,thiophene-based CMPs served as the precursors and doping sources simultaneously. Simple direct carbonization of CMPs produced S-doped carbon materials with highly porous structures. When used as an anode for NIBs, the SCs exhibited a high reversible capacity of 440 mAh g-1at 50 mA g-1after 100 cycles, superior rate capability, and excellent cycling stability(297 mAh g-1after 1000 cycles at 500 mA g-1), outperforming most S-doped carbon materials reported thus far. The excellent performance of the SCs is attributed to the expanded lattice distance after S doping. Furthermore, we employed ex situ X-ray photoelectron spectroscopy to investigate the electrochemical reaction mechanism of the SCs during sodiation–desodiation, which can highlight the role of doped S for Na-ion storage.
引用
收藏
页码:84 / 96
页数:13
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