Interfacial chemistry and structural engineering modified carbon fibers for stable sodium metal anodes

IF 19.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Carbon Energy Pub Date : 2024-08-23 DOI:10.1002/cey2.601
Chenxiao Chu, Chunting Wang, Weisong Meng, Feipeng Cai, Bo Wang, Nana Wang, Jian Yang, Zhongchao Bai
{"title":"Interfacial chemistry and structural engineering modified carbon fibers for stable sodium metal anodes","authors":"Chenxiao Chu, Chunting Wang, Weisong Meng, Feipeng Cai, Bo Wang, Nana Wang, Jian Yang, Zhongchao Bai","doi":"10.1002/cey2.601","DOIUrl":null,"url":null,"abstract":"Sodium (Na) metal stands out as a highly promising anode material for high-energy-density Na batteries owing to its abundant resources and exceptional theoretical capacity at low redox potential. Nevertheless, the uncontrolled growth of Na dendrites and the accompanying volumetric changes during the plating/stripping process lead to safety concerns and poor electrochemical performances. This study introduces nitrogen and oxygen co-doped carbon nanofiber networks wrapped carbon felt (NO-CNCF), serving as Na deposition skeletons to facilitate a highly reversible Na metal anode. The NO-CNCF framework with uniformly distributed “sodiophilic” functional groups, nanonetwork protuberances, and cross-linked network scaffold structure can avoid charge accumulation and facilitate the dendrite-free Na deposition. Benefiting from these features, the NO-CNCF@Na symmetrical cells demonstrate notable enhancements in cycling stability, achieving 4000 h cycles at 1 mA cm<sup>−2</sup> for 1 mAh cm<sup>−2</sup> and 2400 h cycles at 2 mA cm<sup>−2</sup> for 2 mAh cm<sup>−2</sup> with voltage overpotential of approximately 6 and 10 mV, respectively. Furthermore, the NVP//NO-CNCF@Na full cells achieve stable cycling performance and favorable rate capability. This investigation offers novel insights into fabricating a “sodiophilic” matrix with a multistage structure toward high-performance Na metal batteries.","PeriodicalId":33706,"journal":{"name":"Carbon Energy","volume":null,"pages":null},"PeriodicalIF":19.5000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Energy","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/cey2.601","RegionNum":1,"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

Sodium (Na) metal stands out as a highly promising anode material for high-energy-density Na batteries owing to its abundant resources and exceptional theoretical capacity at low redox potential. Nevertheless, the uncontrolled growth of Na dendrites and the accompanying volumetric changes during the plating/stripping process lead to safety concerns and poor electrochemical performances. This study introduces nitrogen and oxygen co-doped carbon nanofiber networks wrapped carbon felt (NO-CNCF), serving as Na deposition skeletons to facilitate a highly reversible Na metal anode. The NO-CNCF framework with uniformly distributed “sodiophilic” functional groups, nanonetwork protuberances, and cross-linked network scaffold structure can avoid charge accumulation and facilitate the dendrite-free Na deposition. Benefiting from these features, the NO-CNCF@Na symmetrical cells demonstrate notable enhancements in cycling stability, achieving 4000 h cycles at 1 mA cm−2 for 1 mAh cm−2 and 2400 h cycles at 2 mA cm−2 for 2 mAh cm−2 with voltage overpotential of approximately 6 and 10 mV, respectively. Furthermore, the NVP//NO-CNCF@Na full cells achieve stable cycling performance and favorable rate capability. This investigation offers novel insights into fabricating a “sodiophilic” matrix with a multistage structure toward high-performance Na metal batteries.

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
用于稳定钠金属阳极的界面化学和结构工程改性碳纤维
金属钠(Na)资源丰富,在低氧化还原电位下具有超强的理论容量,是极具潜力的高能量密度钠电池阳极材料。然而,在电镀/剥离过程中,Na 树枝状突起的不可控生长和随之而来的体积变化会导致安全问题和较差的电化学性能。本研究引入氮氧共掺杂碳纳米纤维网络包裹碳毡(NO-CNCF)作为 Na 沉积骨架,以促进高度可逆的 Na 金属阳极。NO-CNCF骨架具有均匀分布的 "亲钠 "官能团、纳米网络突起和交联网络支架结构,可避免电荷积累,促进无树枝状的Na沉积。得益于这些特点,NO-CNCF@Na 对称电池的循环稳定性显著提高,1 mAh cm-2 的电池在 1 mA cm-2 下可循环 4000 小时,2 mAh cm-2 的电池在 2 mA cm-2 下可循环 2400 小时,过电位电压分别约为 6 mV 和 10 mV。此外,NVP//NO-CNCF@Na 全电池实现了稳定的循环性能和良好的速率能力。这项研究为制造具有多级结构的 "亲钠 "基质以实现高性能镍金属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
Carbon Energy
Carbon Energy Multiple-
CiteScore
25.70
自引率
10.70%
发文量
116
审稿时长
4 weeks
期刊介绍: Carbon Energy is an international journal that focuses on cutting-edge energy technology involving carbon utilization and carbon emission control. It provides a platform for researchers to communicate their findings and critical opinions and aims to bring together the communities of advanced material and energy. The journal covers a broad range of energy technologies, including energy storage, photocatalysis, electrocatalysis, photoelectrocatalysis, and thermocatalysis. It covers all forms of energy, from conventional electric and thermal energy to those that catalyze chemical and biological transformations. Additionally, Carbon Energy promotes new technologies for controlling carbon emissions and the green production of carbon materials. The journal welcomes innovative interdisciplinary research with wide impact. It is indexed in various databases, including Advanced Technologies & Aerospace Collection/Database, Biological Science Collection/Database, CAS, DOAJ, Environmental Science Collection/Database, Web of Science and Technology Collection.
期刊最新文献
Issue Information Cover Image, Volume 6, Number 10, October 2024 Back Cover Image, Volume 6, Number 10, October 2024 Interface and doping engineering of V2C-MXene-based electrocatalysts for enhanced electrocatalysis of overall water splitting Issue Information
×
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