Single-atomic nickel supported on nitrogen-doped porous carbon to boost polysulfide conversion in lithium-sulfur batteries

IF 7.4 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Science China Materials Pub Date : 2024-05-11 DOI:10.1007/s40843-024-2934-9
Leyuan Chen  (, ), Yanyan Sun  (, ), Zhi Chang  (, ), Simin Chai  (, ), Qiong He  (, ), Anqiang Pan  (, )
{"title":"Single-atomic nickel supported on nitrogen-doped porous carbon to boost polysulfide conversion in lithium-sulfur batteries","authors":"Leyuan Chen \n (,&nbsp;),&nbsp;Yanyan Sun \n (,&nbsp;),&nbsp;Zhi Chang \n (,&nbsp;),&nbsp;Simin Chai \n (,&nbsp;),&nbsp;Qiong He \n (,&nbsp;),&nbsp;Anqiang Pan \n (,&nbsp;)","doi":"10.1007/s40843-024-2934-9","DOIUrl":null,"url":null,"abstract":"<div><p>Single-atomic catalysts consisting of atomically dispersed metal sites within nitrogen-doped carbon matrix (M SAC@NC) have emerged as high-performance electrocatalytic materials in Li-S batteries due to their maximum atom utilization, unique physicochemical properties, and superior catalytic activity. In the present work, a series of M SAC@NC (M = Ni, Co, Fe) with similar structural and physicochemical properties have been successfully prepared by the combination of physical adsorption and pyrolysis. The combination of the aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray adsorption spectra indicates the successful formation of single-atomic metal sites. Moreover, the catalytic activity trend toward sulfur redox reaction is observed to be Ni SAC@NC &gt; Co SAC@NC &gt; Fe SAC@NC, and the Ni SAC@NC delivers the highest capacity of 1,280.6 mAh g<sup>−1</sup> and long-time stability at a decay rate of 0.07% per cycle for 800 cycles at 0.5 C, demonstrating excellent battery performance.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"67 6","pages":"1938 - 1946"},"PeriodicalIF":7.4000,"publicationDate":"2024-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s40843-024-2934-9","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Single-atomic catalysts consisting of atomically dispersed metal sites within nitrogen-doped carbon matrix (M SAC@NC) have emerged as high-performance electrocatalytic materials in Li-S batteries due to their maximum atom utilization, unique physicochemical properties, and superior catalytic activity. In the present work, a series of M SAC@NC (M = Ni, Co, Fe) with similar structural and physicochemical properties have been successfully prepared by the combination of physical adsorption and pyrolysis. The combination of the aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray adsorption spectra indicates the successful formation of single-atomic metal sites. Moreover, the catalytic activity trend toward sulfur redox reaction is observed to be Ni SAC@NC > Co SAC@NC > Fe SAC@NC, and the Ni SAC@NC delivers the highest capacity of 1,280.6 mAh g−1 and long-time stability at a decay rate of 0.07% per cycle for 800 cycles at 0.5 C, demonstrating excellent battery performance.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Ni单原子负载氮掺杂多孔碳促进锂硫电池中的多硫化物转化
由原子分散在掺氮碳基质中的金属位点组成的单原子催化剂(M SAC@NC)因其最大程度的原子利用率、独特的物理化学性质和优异的催化活性,已成为锂-S 电池中的高性能电催化材料。本研究采用物理吸附和热解相结合的方法,成功制备了一系列具有相似结构和理化性质的 M SAC@NC(M = Ni、Co、Fe)。结合像差校正高角度环形暗场扫描透射电子显微镜和 X 射线吸附光谱,表明成功形成了单原子金属位点。此外,观察到硫氧化还原反应的催化活性趋势为 Ni SAC@NC > Co SAC@NC > Fe SAC@NC,其中 Ni SAC@NC 在 0.5 C 下循环 800 次,可提供最高容量 1,280.6 mAh g-1,且每次循环的衰减率为 0.07%,表现出优异的电池性能。
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 去求助
来源期刊
Science China Materials
Science China Materials Materials Science-General Materials Science
CiteScore
11.40
自引率
7.40%
发文量
949
期刊介绍: Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.
期刊最新文献
Stress-induced anisotropy for MHz-stable permeability in Fe-based nanocrystalline alloys Synthesis of transition metal nitride nanomaterials for electrocatalytic applications Interface engineering of MXenes for flexible energy storage and harvesting Spatially decoupled single/dual-atomic sites with independent bifunctional activity for high-performance fiber zinc-air batteries Surface-confined metallization of nanofibrous networks via selective dissolution-assisted transfer printing for lightweight and air-permeable soft electronics
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1