High Sulfur Incorporation in Carbon Anodes via Safe Molten-Salt-Assisted Sulfate Doping for Ultrastable Sodium-Ion Batteries

阳极 材料科学 碳纤维 掺杂剂 硫黄 化学工程 电化学 降级(电信) 兴奋剂 熔盐 碳热反应 分解 无机化学 硫酸盐 盐(化学) 沸腾 纳米技术
作者
Xiaolin Li,Jieqi Chen,Zijin Chen,Yashan Hu,Fengqiang Xie,J. Li,Haiyan Zhang,Zhenghui Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:18 (3): 5038-5049
标识
DOI:10.1021/acsami.5c15052
摘要

Sulfur (S)-doped carbon materials have attracted growing interest as promising anode candidates for sodium-ion batteries (SIBs) due to their abundant active sites, large capacity, and fast electrochemical kinetics. However, the current S doping strategies frequently employ elemental S, thiourea, (NH4)2SO4, H2S, etc. as dopants, which have low boiling or decomposition temperatures, bringing along environmental concerns, safety hazards, and fire risks. This study provides an innovative molten-salt-assisted sulfate doping strategy to design S-rich carbon materials. Different from conventional molten-salt systems, it is found that the KCl molten salt and dopant ZnSO4 in this work undergo complicated ion exchange, eutecticum and carbothermal reduction processes, and then release SOx or S to dope the carbon framework. It is demonstrated that the participation of KCl molten salt significantly facilitates the incorporation of S atoms, and the S-doped carbon material retains a S content of 7.3% even at 900 °C, much higher than the blank sample (<3.0%). When employed as an anode for SIBs, this S-doped carbon delivers a reversible capacity of >400 mAh g–1 and demonstrates negligible capacity degradation over 1000 cycles. Notably, highly doped carbon at 900 °C has been rarely achieved, and the employment of highly stable inorganic sulfates as dopants provides many advances such as enhanced safety, low toxicity, and minimal environmental contamination.
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
1秒前
1秒前
北海完成签到,获得积分10
2秒前
失眠忆曼完成签到,获得积分10
2秒前
PERSEVERE完成签到,获得积分10
2秒前
2秒前
ding应助绿泡泡住海边采纳,获得10
5秒前
江三风完成签到,获得积分20
6秒前
思源应助sdl采纳,获得10
6秒前
Oo发布了新的文献求助10
6秒前
dearcih完成签到,获得积分10
7秒前
Akim应助小灰采纳,获得10
7秒前
星耀完成签到,获得积分10
7秒前
伯赏雁蓉发布了新的文献求助10
7秒前
kk_yang发布了新的文献求助30
8秒前
顺心纸鹤完成签到,获得积分10
9秒前
10秒前
10秒前
11秒前
CodeCraft应助江三风采纳,获得10
11秒前
凭亿近人完成签到,获得积分10
12秒前
12秒前
鱿鱼冻煮雨完成签到 ,获得积分10
13秒前
14秒前
15秒前
15秒前
诸葛小哥哥完成签到 ,获得积分0
15秒前
章鱼完成签到 ,获得积分10
16秒前
jiaminzhao完成签到,获得积分10
16秒前
大方的觅海完成签到,获得积分10
16秒前
SnowPeak7完成签到,获得积分10
16秒前
星耀发布了新的文献求助10
17秒前
sdl发布了新的文献求助10
17秒前
18秒前
小郭发布了新的文献求助10
19秒前
20秒前
南宫书瑶发布了新的文献求助10
20秒前
小金完成签到 ,获得积分10
20秒前
as发布了新的文献求助10
22秒前
22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
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rosenblum, Global Change Biology 500
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
DIPPR Project 801 - Full Version 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7767598
求助须知:如何正确求助?哪些是违规求助? 9311142
关于积分的说明 20321997
捐赠科研通 7352630
什么是DOI,文献DOI怎么找? 3315412
关于科研通互助平台的介绍 2464705
邀请新用户注册赠送积分活动 2330053