Mesocrystalline effect boosts the alloying reaction kinetics of Sb2O4 anode in half/full sodium-ion batteries

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL
Ling Guo , Liyun Cao , Jianfeng Huang , Jiayin Li , Yong Zhao , Yijun Liu , Xing Wang , Yishou Wang
{"title":"Mesocrystalline effect boosts the alloying reaction kinetics of Sb2O4 anode in half/full sodium-ion batteries","authors":"Ling Guo ,&nbsp;Liyun Cao ,&nbsp;Jianfeng Huang ,&nbsp;Jiayin Li ,&nbsp;Yong Zhao ,&nbsp;Yijun Liu ,&nbsp;Xing Wang ,&nbsp;Yishou Wang","doi":"10.1016/j.jelechem.2024.118753","DOIUrl":null,"url":null,"abstract":"<div><div>Mesocrystalline materials are reported to show great advantages in improving electrochemical performance. However, there are no reports about mesocrystalline Sb<sub>2</sub>O<sub>4</sub> anode, and the structure advantage in reaction kinetics is unclear. In this work, we have prepared a mesocrystalline Sb<sub>2</sub>O<sub>4</sub> structure (M−Sb<sub>2</sub>O<sub>4</sub>) in a facile hydrothermal process and further explored the structure effect on reaction kinetics. The exploration results show that the micro-flower mesocrystalline M−Sb<sub>2</sub>O<sub>4</sub> consists of oriented nanowires with (110) crystal faces showing large surface area and high porosity. This structure can increase the contact area between electrode and electrolyte, provide fast Na<sup>+</sup> transfer channels, and shorten the charge transport path, exhibiting excellent alloying reaction kinetics. The excellent reaction kinetics improves rate performance with a capacity of 432 mA h g<sup>-1</sup> at 5 A g<sup>-1</sup>. Furthermore, it exhibits a high power density of 1700 W kg<sup>−1</sup> in the full cell. Compared to the other reported various structured Sb-based anodes, M−Sb<sub>2</sub>O<sub>4</sub> exhibits a great performance advantage. This work demonstrates that the mesocrystalline effect can effectively enhance alloying reaction kinetics, providing a new strategy for performance optimization of other alloy-based anodes.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"974 ","pages":"Article 118753"},"PeriodicalIF":4.1000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665724007318","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Mesocrystalline materials are reported to show great advantages in improving electrochemical performance. However, there are no reports about mesocrystalline Sb2O4 anode, and the structure advantage in reaction kinetics is unclear. In this work, we have prepared a mesocrystalline Sb2O4 structure (M−Sb2O4) in a facile hydrothermal process and further explored the structure effect on reaction kinetics. The exploration results show that the micro-flower mesocrystalline M−Sb2O4 consists of oriented nanowires with (110) crystal faces showing large surface area and high porosity. This structure can increase the contact area between electrode and electrolyte, provide fast Na+ transfer channels, and shorten the charge transport path, exhibiting excellent alloying reaction kinetics. The excellent reaction kinetics improves rate performance with a capacity of 432 mA h g-1 at 5 A g-1. Furthermore, it exhibits a high power density of 1700 W kg−1 in the full cell. Compared to the other reported various structured Sb-based anodes, M−Sb2O4 exhibits a great performance advantage. This work demonstrates that the mesocrystalline effect can effectively enhance alloying reaction kinetics, providing a new strategy for performance optimization of other alloy-based anodes.

Abstract Image

介晶效应促进了半/全钠离子电池中 Sb2O4 阳极的合金化反应动力学
据报道,介晶材料在提高电化学性能方面具有很大优势。然而,目前还没有关于介晶 Sb2O4 阳极的报道,其在反应动力学中的结构优势也不明确。在这项工作中,我们采用简便的水热法制备了介晶 Sb2O4 结构(M-Sb2O4),并进一步探讨了该结构对反应动力学的影响。研究结果表明,微花介晶 M-Sb2O4 由取向纳米线组成,晶面为(110),具有大表面积和高孔隙率。这种结构可以增加电极与电解液的接触面积,提供快速的 Na+ 传输通道,缩短电荷传输路径,表现出优异的合金化反应动力学。优异的反应动力学提高了速率性能,在 5 A g-1 的条件下,容量可达 432 mA h g-1。此外,它在全电池中还表现出 1700 W kg-1 的高功率密度。与其他已报道的各种结构的锑基阳极相比,M-Sb2O4 具有极大的性能优势。这项研究表明,介晶效应能有效提高合金化反应动力学,为其他合金基阳极的性能优化提供了一种新策略。
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 求助全文
来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信