Regulation of Li2S Deposition and Dissolution to Achieve an Efficient Bidirectional Lithium–Sulfur Battery

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2025-01-16 DOI:10.1002/adfm.202421900
Dan You, Wenhao Yang, Yongshun Liang, Chunman Yang, Yiwei Yu, Ziyi Zhu, Xue Li, Yiyong Zhang, Yingjie Zhang
{"title":"Regulation of Li2S Deposition and Dissolution to Achieve an Efficient Bidirectional Lithium–Sulfur Battery","authors":"Dan You,&nbsp;Wenhao Yang,&nbsp;Yongshun Liang,&nbsp;Chunman Yang,&nbsp;Yiwei Yu,&nbsp;Ziyi Zhu,&nbsp;Xue Li,&nbsp;Yiyong Zhang,&nbsp;Yingjie Zhang","doi":"10.1002/adfm.202421900","DOIUrl":null,"url":null,"abstract":"<p>Promoting the sulfur reduction reaction (SRR) and sulfur evolution reaction (SER) kinetics is crucial for practical lithium–sulfur batteries. However, the electrode will be passivated by insulated Li<sub>2</sub>S if blindly accelerated the SRR kinetics, meanwhile, the high activation energy of Li<sub>2</sub>S will lead to premature the oxidation of Li<sub>2</sub>S (SER), achieving limited catalyst. Here, a nano-nickel nitrogen-doped carbon gel material (CG/Ni) induces the instantaneous nucleation, further endows Li<sub>2</sub>S fast ion/electron transfer, resulting porous 3D growth instead single lateral growth. Therefore, CG/Ni material avoids being passivated, accelerating the SRR kinetics. Meanwhile, CG/Ni decreases the delithiation barrier, thus, facilitating the Li<sub>2</sub>S dissociation. Both experiments and theory calculation prove that CG/Ni achieves efficient bidirectional catalysis. Consequently, CG/Ni cathode delivers a low-capacity decay ratio of 0.047% per cycle for 900 cycles at 5 C. This work unlocks a bidirectional catalyst and provide new insight for high-efficiency lithium–sulfur batteries.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 20","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202421900","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Promoting the sulfur reduction reaction (SRR) and sulfur evolution reaction (SER) kinetics is crucial for practical lithium–sulfur batteries. However, the electrode will be passivated by insulated Li2S if blindly accelerated the SRR kinetics, meanwhile, the high activation energy of Li2S will lead to premature the oxidation of Li2S (SER), achieving limited catalyst. Here, a nano-nickel nitrogen-doped carbon gel material (CG/Ni) induces the instantaneous nucleation, further endows Li2S fast ion/electron transfer, resulting porous 3D growth instead single lateral growth. Therefore, CG/Ni material avoids being passivated, accelerating the SRR kinetics. Meanwhile, CG/Ni decreases the delithiation barrier, thus, facilitating the Li2S dissociation. Both experiments and theory calculation prove that CG/Ni achieves efficient bidirectional catalysis. Consequently, CG/Ni cathode delivers a low-capacity decay ratio of 0.047% per cycle for 900 cycles at 5 C. This work unlocks a bidirectional catalyst and provide new insight for high-efficiency lithium–sulfur batteries.

Abstract Image

Abstract Image

Abstract Image

Abstract Image

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
调控Li2S沉积和溶解以实现高效的双向锂硫电池
提高硫还原反应(SRR)和硫析反应(SER)动力学对锂硫电池的实际应用至关重要。然而,如果盲目加速SRR动力学,则电极将被绝缘Li2S钝化,同时Li2S的高活化能将导致Li2S (SER)过早氧化,达到催化剂的限制。在这里,纳米镍氮掺杂碳凝胶材料(CG/Ni)诱导瞬时成核,进一步赋予Li2S快速离子/电子转移,导致多孔三维生长而不是单侧生长。因此,CG/Ni材料避免了钝化,加速了SRR动力学。同时,CG/Ni降低了氧化障碍,有利于Li2S的解离。实验和理论计算均证明了CG/Ni实现了高效的双向催化。因此,CG/Ni阴极在5℃下循环900次,每循环的低容量衰减率为0.047%。这项工作解开了双向催化剂,并为高效锂硫电池提供了新的见解。
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
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
期刊最新文献
Fibrillar Morphology Realized by Regulating Self‐Aggregation and Crystallization Kinetics from Non‐Volatile Solid Additives for Efficient Polymer Solar Cells Reevaluating the Activity of ZIF‐8 Based FeNCs for Electrochemical Ammonia Production Enabling Free Growth of Thin Films by Magnetron Sputtering for Blooming Microstructures Electron Delocalization Engineering on 2D High‐Entropy Metal Oxides for Boosting Electromagnetic Wave Absorption Bipolar Carrier Transport of GaO x via Doping and Defect Engineering for High‐Efficiency Silicon Heterojunction Solar Cells
×
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