Ramie Degumming Waste-Derived Nitrogen and Molybdenum Dual-Doped Porous Carbon for High-Performance Lithium–Sulfur Batteries

IF 2.6 4区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ChemNanoMat Pub Date : 2024-06-26 DOI:10.1002/cnma.202400311
Dr. Zhehan Yang, Qingling Ruan, Prof. Tiezhu Chen, Dr. Xiaolei Ren, Juan Lin, Prof. Xingxing Gu
{"title":"Ramie Degumming Waste-Derived Nitrogen and Molybdenum Dual-Doped Porous Carbon for High-Performance Lithium–Sulfur Batteries","authors":"Dr. Zhehan Yang,&nbsp;Qingling Ruan,&nbsp;Prof. Tiezhu Chen,&nbsp;Dr. Xiaolei Ren,&nbsp;Juan Lin,&nbsp;Prof. Xingxing Gu","doi":"10.1002/cnma.202400311","DOIUrl":null,"url":null,"abstract":"<p>The high energy density and low cost of sulfur make lithium–sulfur batteries one of the most promising candidates for the next generation of energy storage. Nevertheless, the application is still hampered by the shuttle effect of soluble lithium polysulfides (LiPSs) intermediates and slow redox kinetics, resulting in irreversible loss of the active material, severe self-discharge and poor cycle stability of the electrode. Therefore, in this work, a novel Mo,N co-doped porous carbon (Mo,N−C) was successfully synthesized by simply calcining a mixture of ramie degumming waste with cost-effective molybdenum salt, and then employed as the LiPSs anchor. Due to the conductive carbon matrix, abundant porous structures as well as the doping Mo and N heteroatoms, the sluggish redox kinetic of the cathode has been significantly improved and the shuttle phenomenon of LiPSs has been effectively inhibited, consequently, the as-prepared Mo,N−C/S-0.4 composite cathode could demonstrate a good initial capacity of 1379.2 mAh g<sup>−1</sup> at 0.2 C, and the reversible capacity could remain at 997.5 mAh g<sup>−1</sup> after 100 cycles. Even at a high discharge rate of 1.0 C, the capacity could remain at 700.2 mAh g<sup>−1</sup> after 400 cycles. This work provides a new avenue for utilizing waste biomass in clean energy storage.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"10 10","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemNanoMat","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cnma.202400311","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The high energy density and low cost of sulfur make lithium–sulfur batteries one of the most promising candidates for the next generation of energy storage. Nevertheless, the application is still hampered by the shuttle effect of soluble lithium polysulfides (LiPSs) intermediates and slow redox kinetics, resulting in irreversible loss of the active material, severe self-discharge and poor cycle stability of the electrode. Therefore, in this work, a novel Mo,N co-doped porous carbon (Mo,N−C) was successfully synthesized by simply calcining a mixture of ramie degumming waste with cost-effective molybdenum salt, and then employed as the LiPSs anchor. Due to the conductive carbon matrix, abundant porous structures as well as the doping Mo and N heteroatoms, the sluggish redox kinetic of the cathode has been significantly improved and the shuttle phenomenon of LiPSs has been effectively inhibited, consequently, the as-prepared Mo,N−C/S-0.4 composite cathode could demonstrate a good initial capacity of 1379.2 mAh g−1 at 0.2 C, and the reversible capacity could remain at 997.5 mAh g−1 after 100 cycles. Even at a high discharge rate of 1.0 C, the capacity could remain at 700.2 mAh g−1 after 400 cycles. This work provides a new avenue for utilizing waste biomass in clean energy storage.

Abstract Image

苎麻脱胶废物衍生生物质碳用于高性能锂硫电池
可溶性多硫化锂(LiPSs)中间体的穿梭效应和缓慢的氧化还原动力学仍然阻碍着锂硫电池(LSBs)的应用。因此,本研究通过简单煅烧苎麻脱胶废料与高性价比钼盐的混合物,成功合成了一种新型 Mo,N 共掺杂多孔碳(Mo,N-C),并将其用作锂多硫化物锚。由于碳基体的导电性、丰富的多孔结构以及掺杂的 Mo 和 N 杂原子,阴极缓慢的氧化还原动力学得到了显著改善,并有效抑制了 LiPSs 的穿梭现象,因此,合成的 Mo,N-C/S-0.4 复合阴极在 0.2 C 下可显示出 1379.2 mAh g-1 的良好初始容量,100 个循环后可逆容量仍可保持在 997.5 mAh g-1 左右。即使在 1.0 C 的高放电率下,400 个循环后的容量仍能保持在 700.2 mAh g-1 的水平。这项工作为利用废弃生物质进行清洁能源储存提供了一条新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ChemNanoMat
ChemNanoMat Energy-Energy Engineering and Power Technology
CiteScore
6.10
自引率
2.60%
发文量
236
期刊介绍: ChemNanoMat is a new journal published in close cooperation with the teams of Angewandte Chemie and Advanced Materials, and is the new sister journal to Chemistry—An Asian Journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信