Conjugated microporous polymer derived N, O and S co-doped sheet-like carbon materials as anode materials for high-performance lithium-ion batteries

被引:19
作者
Li, Chunxia [1 ]
Kong, Dehao [3 ]
Wang, Bo [1 ]
Du, Hongmei [1 ]
Zhao, Jinsheng [1 ]
Dong, Yunyun [1 ]
Xie, Yu [2 ]
机构
[1] Liaocheng Univ, Coll Chem & Chem Engn, Liaocheng 252059, Shandong, Peoples R China
[2] Nanchang Hangkong Univ, Coll Environm & Chem Engn, Nanchang 330063, Jiangxi, Peoples R China
[3] Guangxi Univ Sci & Technol, Sch Elect & Informat Engn, Liuzhou 545006, Peoples R China
基金
中国国家自然科学基金;
关键词
N; O and S co-doped; covalent organic framework; electrochemical performance; lithium-ion batteries; anode materials; COVALENT ORGANIC FRAMEWORK; NITROGEN; MICROSPHERES; STABILITY; COMPOSITE; CAPACITY;
D O I
10.1016/j.jtice.2022.104293
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Rational design and preparation of nitrogen (N), oxygen (O), and sulfur (S) co-doped materials with distinguished electrochemical performance in lithium-ion batteries are highly sensible. In this study, layered structure carbon material (PTPAO@600) with co-doped N, O and S elements is prepared by carbonizing conjugated microporous polymers (CMPs) as a precursor. When PTPAO@600 electrode material employed as anode of LIBs, and evaluated its properties in electrochemical aspects. After cycling for 800 times under 0.1 A g (1), PTPAO@600 electrode has shown powerful reversible specific capacity of 1142.5 mAh g (1), and excellent rate capability of 275 mAh g (1) at 2.0 A g (1) large current density. Long-cycle performance for 1000 charge/discharge cycles shows that the capacity is retained at 490.9 mAh g (1) under 1.0 A g (1), revealing its high stability. Such high lithium storage performance is mainly attributed to rich heteroatom co-doping, larger specific surface area and high Li+ diffusion coefficient. The superior electrochemical performance makes the PTPAO@600 a anode material with potential in secondary batteries. (c) 2022 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
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页数:10
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