Anode of Anthracite Hard Carbon Hybridized by Phenolic Epoxy Resin toward Enhanced Performance for Sodium-Ion Batteries

环氧树脂 阳极 无烟煤 碳纤维 离子 材料科学 化学工程 化学 复合材料 冶金 有机化学 电极 复合数 工程类 物理化学
作者
Qingqing Wang,Zhuang Hu,Ruisheng Zhang,Changling Fan,Jinshui Liu,Jinshui Liu,Jilei Liu,Jilei Liu
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:7 (15): 6704-6716 被引量:26
标识
DOI:10.1021/acsaem.4c01310
摘要

Anthracite-based carbon is considered one of the most promising anodes for sodium-ion batteries (SIBs) due to its abundant natural resource and low cost. However, their performance is very poor. In this article, the microstructure of anthracite is hybridized by phenolic epoxy resin. The cross-linking reaction between anthracite and the resin generates hybrid carbon. The structure of anthracite transforms from graphite-like phase to pseudographite phase, accompanied by the increase of interlayer spacing. Due to the formation of oxygen-containing functional groups, abundant defects are generated on the surface and inside. Phenolic epoxy resin generates a microhard carbon structure around anthracite, in which curved and intertwined disordered structure are formed. This can effectively reduce the degree of graphitization of anthracite, promote rearrangement, and inhibit the regular accumulation of carbon layers. The performance of the anthracite anode with 5% resin pyrolyzed at 1200 °C is improved obviously, delivering capacity of 357.7 mAh g–1 at a current density of 50 mA g–1 and excellent capacity retention of 89% after 500 cycles at 500 mA g–1. According to the in situ Raman analysis, it can be seen that Na+ is mainly adsorbed on the defect sites and open pore gaps on the material surface and then inserted in the pseudographitic region. This research proposes an effective strategy to enhance the performance of natural coal carbon material, providing huge opportunity for the commercialization of low-cost anthracite anodes for SIBs.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
香蕉觅云应助科研通管家采纳,获得10
刚刚
刚刚
酷波er应助科研通管家采纳,获得10
刚刚
刚刚
刚刚
不饱和环二酮完成签到,获得积分10
刚刚
糊涂的小鸭子完成签到,获得积分10
1秒前
pupu完成签到,获得积分10
1秒前
1秒前
lkk完成签到,获得积分10
1秒前
娜娜完成签到 ,获得积分10
2秒前
Nicole完成签到,获得积分10
2秒前
2秒前
Kaaaly完成签到 ,获得积分10
2秒前
今晚吃螺蛳粉完成签到,获得积分10
2秒前
Cynthia发布了新的文献求助10
3秒前
耙芋儿完成签到,获得积分10
3秒前
飞0802完成签到,获得积分10
3秒前
斯文败类应助万幸鹿采纳,获得10
3秒前
3秒前
七七爱学习完成签到,获得积分10
3秒前
魔幻飞风发布了新的文献求助10
4秒前
4秒前
4秒前
华仔应助weiiioyo采纳,获得10
4秒前
Lil_Bear完成签到,获得积分10
4秒前
dougsong发布了新的文献求助10
5秒前
nnl完成签到,获得积分10
5秒前
白白白白白柏完成签到,获得积分10
5秒前
5秒前
CodeCraft应助残剑月采纳,获得10
6秒前
Sylvie完成签到,获得积分20
6秒前
卡卡发布了新的文献求助10
6秒前
hcx完成签到,获得积分10
7秒前
orixero应助月初采纳,获得10
7秒前
dbc1234完成签到,获得积分10
7秒前
long完成签到,获得积分10
7秒前
kelly发布了新的文献求助10
8秒前
AR完成签到,获得积分10
8秒前
mmr完成签到,获得积分10
8秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics 500
A Social and Cultural History of the Hellenistic World 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6395083
求助须知:如何正确求助?哪些是违规求助? 8210105
关于积分的说明 17386238
捐赠科研通 5448298
什么是DOI,文献DOI怎么找? 2880111
邀请新用户注册赠送积分活动 1856628
关于科研通互助平台的介绍 1699314