Pore structure regulation of hard carbon: Towards fast and high-capacity sodium-ion storage

被引:70
|
作者
Yang, Le [1 ,2 ]
Hu, Mingxiang [2 ]
Zhang, Hongwei [2 ]
Yang, Wen [1 ]
Lv, Ruitao [2 ,3 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing Key Lab Photoelect Electrophoton Convers, Key Lab Cluster Sci,Minist Educ, Beijing 100081, Peoples R China
[2] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat MOE, Beijing 100084, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Micropore; Mesopore; Pore-structure evolution; Hard carbon; Anode; Sodium-ion battery; HIGH-PERFORMANCE ANODE; SUPERIOR LONG-LIFE; RATE CAPABILITY; LITHIUM-ION; NANOFIBERS; BATTERIES; MICROSPHERES; ELECTRODES; INSERTION; GRAPHENE;
D O I
10.1016/j.jcis.2020.01.085
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
Hard carbon is regarded as one of the most promising anode material for sodium-ion batteries in virtue of the low cost and stable framework. However, the correlation between pore structures of hard carbon and sodium-ion storage is still ambiguous. In this work, based on precise control of pore-size distribution, the capacity, ion diffusion, and initial Coulombic efficiency were improved. Meanwhile, the relationship between pore structure and capacity was investigated. Our result indicates that the micropores hinder ion diffusion and hardly ever accommodate Na+ ions, while mesopores facilitate Na' ion intercalation. Hard carbon with negligible micropores and abundant mesopores delivers a maximum capacity of 283.7 mAh g(-1) at 20 mA g(-1), which is 83% higher than that of micropore-rich one. Even after 320 cycles at 200 mA g(-1), the capacity still remains 189.4 mAh g(-1). (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 264
页数:8
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