Anchoring intermediate phases via few-layer MoSSe nanosheets in flexible porous carbon fiber for stable lithium ion storage

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2025-01-03 DOI:10.1039/d4ta07595a
Mengluan Gao, Zhe Cui, Jingqi Zhu, Rujia Zou, Wenqing Wang, Ye Chen, Huifang Chen
{"title":"Anchoring intermediate phases via few-layer MoSSe nanosheets in flexible porous carbon fiber for stable lithium ion storage","authors":"Mengluan Gao, Zhe Cui, Jingqi Zhu, Rujia Zou, Wenqing Wang, Ye Chen, Huifang Chen","doi":"10.1039/d4ta07595a","DOIUrl":null,"url":null,"abstract":"Transition metal chalcogenides (TMCs) have been widely studied as anode materials for lithium-ion batteries (LIBs) due to their high specific capacity properties. However, the dissolution and agglomeration of the unstable reaction intermediate lithium polysulfide inevitably leads to a significant loss of the active ingredient and a reduction in the reversibility of the reaction, resulting in a shortened lifetime. Herein, we successful constructed few-layered ultrathin MoSSe nanosheets embedded in flexible porous carbon nanofibers (MoSSe/CNFs).Firstly, MoSSe/CNFs not only confers superior flexibility and integrity to the carbon fibers through a network of large pores but also enhances the fast electron transport capability. Secondly, the optimized Se-doped MoS3 inside the CNFs structure is formed after the first discharge/charge cycles, can prevent detrimental interfacial side reactions, decrease the Li+ diffusion barriers, increase electronic conductivity, and limit the dissolution of polysulfides or polyselenides in the electrolyte. Finally, the N-doped flexible porous carbon nanofiber accommodates the volume expansion, prevents the aggregation issues of MoS3 and irreversible decomposition of Li2S or Li2Se into the electrolyte ,which can benefit greatly in reaction kinetics and structural stability for improved lithium storage performance. As a result of these improvements, the self-standing MoSSe/CNFs electrodes show a stable capacity of 738 mAh g-1 at 0.5 A g-1 and 578 mAh g-1 at 5 A g-1 with the capacity retention of almost 100% over 950 cycles.","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":"41 1","pages":""},"PeriodicalIF":10.7000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4ta07595a","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Transition metal chalcogenides (TMCs) have been widely studied as anode materials for lithium-ion batteries (LIBs) due to their high specific capacity properties. However, the dissolution and agglomeration of the unstable reaction intermediate lithium polysulfide inevitably leads to a significant loss of the active ingredient and a reduction in the reversibility of the reaction, resulting in a shortened lifetime. Herein, we successful constructed few-layered ultrathin MoSSe nanosheets embedded in flexible porous carbon nanofibers (MoSSe/CNFs).Firstly, MoSSe/CNFs not only confers superior flexibility and integrity to the carbon fibers through a network of large pores but also enhances the fast electron transport capability. Secondly, the optimized Se-doped MoS3 inside the CNFs structure is formed after the first discharge/charge cycles, can prevent detrimental interfacial side reactions, decrease the Li+ diffusion barriers, increase electronic conductivity, and limit the dissolution of polysulfides or polyselenides in the electrolyte. Finally, the N-doped flexible porous carbon nanofiber accommodates the volume expansion, prevents the aggregation issues of MoS3 and irreversible decomposition of Li2S or Li2Se into the electrolyte ,which can benefit greatly in reaction kinetics and structural stability for improved lithium storage performance. As a result of these improvements, the self-standing MoSSe/CNFs electrodes show a stable capacity of 738 mAh g-1 at 0.5 A g-1 and 578 mAh g-1 at 5 A g-1 with the capacity retention of almost 100% over 950 cycles.
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
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
期刊最新文献
Highly conductive PANI/ATMP/AgNO3 composite hydrogel electrodes for all-hydrogel-state supercapacitors Metastable State Structure Promotes Surface Reconstruction of Spinel NiFe2O4 for Efficient Oxygen Evolution Reaction Anchoring intermediate phases via few-layer MoSSe nanosheets in flexible porous carbon fiber for stable lithium ion storage Sulfur-based hybrid multilayers on Li metal anodes with excellent air stability for ultralong-life and high-performance batteries Amorphous-like thermal conductivity and high thermoelectric figure of merit in “π” SnS and SnSe
×
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:481959085
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