Nanoporous Graphene with Encapsulated Multicomponent Carbide as High-Performance Binder-Free Lithium-Ion Battery Anodes

IF 9.1 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Small Methods Pub Date : 2025-03-13 DOI:10.1002/smtd.202401974
Linshan Zhu, Naixuan Ci, Guoan Wang, Yixuan Hu, Haiyun Zhang, Xin Wu, Boxuan Cao, Guoqiang Xie, Xingjun Liu, Kolan Madhav Reddy, Hua-Jun Qiu
{"title":"Nanoporous Graphene with Encapsulated Multicomponent Carbide as High-Performance Binder-Free Lithium-Ion Battery Anodes","authors":"Linshan Zhu,&nbsp;Naixuan Ci,&nbsp;Guoan Wang,&nbsp;Yixuan Hu,&nbsp;Haiyun Zhang,&nbsp;Xin Wu,&nbsp;Boxuan Cao,&nbsp;Guoqiang Xie,&nbsp;Xingjun Liu,&nbsp;Kolan Madhav Reddy,&nbsp;Hua-Jun Qiu","doi":"10.1002/smtd.202401974","DOIUrl":null,"url":null,"abstract":"<p>Metal carbides are considered attractive lithium-ion battery (LIB) anode materials. Their potential practical application, however, still needs nanostructure optimization to further enhance the Li-storage capacity, especially under large current densities. Herein, a nanoporous structured multi-metal carbide is designed, which is encapsulated in a 3D free-standing nanotubular graphene film (MnNiCoFe-MoC@NG). This free-standing composite anode with a high surface area not only provides more active Li<sup>+</sup> storage sites but also effectively prevents the agglomeration or detachment of active material in traditional powder-based electrodes. Moreover, the free-standing design does not require additional binders, conductive agents, or even current collectors when used as LIB anode. As a result, the MnNiCoFe-MoC@NG anode exhibits a high specific capacity of 1129.2 mAh g<sup>−1</sup> at 2 A g<sup>−1</sup> and maintains a stable capacity of 512.9 mAh g<sup>−1</sup> after 2900 cycles of 5 A g<sup>−1</sup>, which is higher than most reported Mo<sub>x</sub>C-based anodes. Furthermore, the anode exhibits superb low-temperature performance at both 0 and −20 °C, especially at large current densities. These properties make the free-standing anode very promising in fast charging and low-temperature applications.</p>","PeriodicalId":229,"journal":{"name":"Small Methods","volume":"9 7","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small Methods","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smtd.202401974","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

Metal carbides are considered attractive lithium-ion battery (LIB) anode materials. Their potential practical application, however, still needs nanostructure optimization to further enhance the Li-storage capacity, especially under large current densities. Herein, a nanoporous structured multi-metal carbide is designed, which is encapsulated in a 3D free-standing nanotubular graphene film (MnNiCoFe-MoC@NG). This free-standing composite anode with a high surface area not only provides more active Li+ storage sites but also effectively prevents the agglomeration or detachment of active material in traditional powder-based electrodes. Moreover, the free-standing design does not require additional binders, conductive agents, or even current collectors when used as LIB anode. As a result, the MnNiCoFe-MoC@NG anode exhibits a high specific capacity of 1129.2 mAh g−1 at 2 A g−1 and maintains a stable capacity of 512.9 mAh g−1 after 2900 cycles of 5 A g−1, which is higher than most reported MoxC-based anodes. Furthermore, the anode exhibits superb low-temperature performance at both 0 and −20 °C, especially at large current densities. These properties make the free-standing anode very promising in fast charging and low-temperature applications.

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
纳米多孔石墨烯封装多组分碳化物作为高性能无粘结剂锂离子电池阳极。
金属碳化物是锂离子电池极具吸引力的负极材料。然而,其潜在的实际应用仍需要纳米结构优化,以进一步提高锂存储容量,特别是在大电流密度下。本文设计了一种纳米多孔结构的多金属碳化物,并将其封装在三维独立的纳米管石墨烯薄膜中(MnNiCoFe-MoC@NG)。这种具有高表面积的独立复合阳极不仅提供了更多的活性Li+存储位点,而且有效地防止了传统粉末基电极中活性材料的团聚或脱离。此外,独立设计不需要额外的粘合剂,导电剂,甚至电流收集器当用作锂离子电池阳极时。结果表明,MnNiCoFe-MoC@NG阳极在2 a g-1下具有1129.2 mAh g-1的高比容量,在5 a g-1下循环2900次后保持512.9 mAh g-1的稳定容量,高于大多数moc基阳极。此外,阳极在0°C和-20°C下都表现出极好的低温性能,特别是在大电流密度下。这些特性使得独立阳极在快速充电和低温应用中非常有前景。
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
Small Methods
Small Methods Materials Science-General Materials Science
CiteScore
17.40
自引率
1.60%
发文量
347
期刊介绍: Small Methods is a multidisciplinary journal that publishes groundbreaking research on methods relevant to nano- and microscale research. It welcomes contributions from the fields of materials science, biomedical science, chemistry, and physics, showcasing the latest advancements in experimental techniques. With a notable 2022 Impact Factor of 12.4 (Journal Citation Reports, Clarivate Analytics, 2023), Small Methods is recognized for its significant impact on the scientific community. The online ISSN for Small Methods is 2366-9608.
期刊最新文献
Beyond the Hype: Decoding Bis(fluorosulfonyl)imide Chemistry in Advanced Lithium-Sulfur Batteries. Improving Cycle Life and Capacity Retention in PVMPO‖Li Dual-Ion Lithium-Organic Batteries Using an EC-Free and FEC Additive Containing Electrolyte. Naphthalene-Based Passivators for Efficient Perovskite Solar Cells: Synergistic Defect Passivation and Charge Extraction via Combined Theoretical and Experimental Study. Correction to: "Environment-Adaptable Rotational Energy Harvesters Based on Nylon-Core Coiled Carbon Nanotube Yarns". Cardenolide-Engineered Extracellular Vesicles Augment Drug Uptake and Cytotoxicity in Non-small Cell Lung Cancer 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