Si@nitrogen-doped porous carbon derived from covalent organic framework for enhanced Li-storage

被引:26
|
作者
Chen, Kaixiang [1 ]
Xiong, Jinyong [1 ]
Yu, Hao [1 ]
Wang, Li [1 ]
Song, Yonghai [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Natl Engn Res Ctr Carbohydrate Synth, Key Lab Fluorine & Silicon Energy Mat & Chem Minis, 99 Ziyang Rd, Nanchang 330022, Peoples R China
基金
中国国家自然科学基金;
关键词
Covalent organic frameworks; Nitrogen-doped carbon; Core-shell structure; Nano-Si; Lithium-ion batteries; Anode; PERFORMANCE LITHIUM-ION; ANODE MATERIAL; COMPOSITE; HYBRID; NANOPARTICLES;
D O I
10.1016/j.jcis.2022.12.058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Due to ultra-high theoretical capacity (4200 mAh g-1), silicon (Si) is an excellent candidate for the anode of lithium-ion batteries (LIBs). However, the application of Si is severely limited by its volume expansion of approximately 300% during the charge/discharge process. Herein, nitrogen-doped porous carbon (NC) capped nano-Si particles (Si@NC) composites with a core-shell structure were obtained by calcination of covalent organic frameworks (COFs) encapsulated nano-Si. COFs is a crystalline material with well -ordered structures, adjustable and ordered pores and abundant N atoms. After carbonization, the well -ordered pores and frameworks were kept well. Compared with other Si@NC composites, the well-ordered NC framework shell derived from COFs possesses high elasticity and well-ordered pores, which provides space for the volume expansion of nano-Si, and a channel to transfer Li'. The core-shell Si@NC composite exhibited good performances when applied as the anode of LIBs. At a current density of 100 mA g-1, it exhib-ited a discharge-specific capacity of 1534.8 mAh g-1 after 100 cycles with a first-coulomb efficiency of 69.7%. The combination of COFs with nano-Si is a better strategy for the preparation of anode materials of LIBs. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 184
页数:9
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