镍锰-LDH 纳米片的 H-空穴诱导 Mn2+ 高效沉积,用于制造耐用的锌离子电池

IF 18.9 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Energy Storage Materials Pub Date : 2024-11-05 DOI:10.1016/j.ensm.2024.103887
Junpeng Li , Xubo Yang , Jinwei Wang , Chunjie Ma , Tingxia Wang , Nailiang Liu , Xiufen Pang , Qian Zhang , Chao Wu , Xifei Li
{"title":"镍锰-LDH 纳米片的 H-空穴诱导 Mn2+ 高效沉积,用于制造耐用的锌离子电池","authors":"Junpeng Li ,&nbsp;Xubo Yang ,&nbsp;Jinwei Wang ,&nbsp;Chunjie Ma ,&nbsp;Tingxia Wang ,&nbsp;Nailiang Liu ,&nbsp;Xiufen Pang ,&nbsp;Qian Zhang ,&nbsp;Chao Wu ,&nbsp;Xifei Li","doi":"10.1016/j.ensm.2024.103887","DOIUrl":null,"url":null,"abstract":"<div><div>The dissolution of Mn-based oxides cathodes is an urgent issue, as it leads to electrochemically irreversible byproducts and, finally, battery failure. In this work, activated NiMn-LDHv nanosheets with H vacancies are proposed as the cathode material for durable zinc ion batteries. The H vacancies promote Mn<sup>2+</sup> deposition by redistributing the electron density and building strong Mn-O bonds, as a result, endowing NiMn-LDHv with the ability of controllable back-deposition of Mn<sup>2+</sup>. It's verified that MnO<sub>2</sub> is deposited on the NiMn-LHDv substrate during charging, the dissolution and the Zn<sup>2+</sup>/H<sup>+</sup> co-intercalation of MnO<sub>2</sub> have a combined contribution to the discharge capacity. The full battery with NiMn-LDHv cathode delivers rate capacity of 258 mAh g<sup>−1</sup> at 0.3 A g<sup>−1</sup>, and even 90 mAh g<sup>−1</sup> at 11.0 A g<sup>−1</sup>. Furthermore, the irreversible Mn-based byproducts are inhibited, resulting in durable cycling performance. After 2500 charge/discharge cycles, the initial capacity remains 91 %. This work provides an important strategy to utilize Mn<sup>2+</sup> efficiently and develop a robust Mn-based cathode, which could greatly prompt the practical application of aqueous zinc ion batteries.</div></div>","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"74 ","pages":"Article 103887"},"PeriodicalIF":18.9000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly efficient Mn2+ deposition induced by H-vacancies of NiMn-LDH nanosheets for durable zinc ion batteries\",\"authors\":\"Junpeng Li ,&nbsp;Xubo Yang ,&nbsp;Jinwei Wang ,&nbsp;Chunjie Ma ,&nbsp;Tingxia Wang ,&nbsp;Nailiang Liu ,&nbsp;Xiufen Pang ,&nbsp;Qian Zhang ,&nbsp;Chao Wu ,&nbsp;Xifei Li\",\"doi\":\"10.1016/j.ensm.2024.103887\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The dissolution of Mn-based oxides cathodes is an urgent issue, as it leads to electrochemically irreversible byproducts and, finally, battery failure. In this work, activated NiMn-LDHv nanosheets with H vacancies are proposed as the cathode material for durable zinc ion batteries. The H vacancies promote Mn<sup>2+</sup> deposition by redistributing the electron density and building strong Mn-O bonds, as a result, endowing NiMn-LDHv with the ability of controllable back-deposition of Mn<sup>2+</sup>. It's verified that MnO<sub>2</sub> is deposited on the NiMn-LHDv substrate during charging, the dissolution and the Zn<sup>2+</sup>/H<sup>+</sup> co-intercalation of MnO<sub>2</sub> have a combined contribution to the discharge capacity. The full battery with NiMn-LDHv cathode delivers rate capacity of 258 mAh g<sup>−1</sup> at 0.3 A g<sup>−1</sup>, and even 90 mAh g<sup>−1</sup> at 11.0 A g<sup>−1</sup>. Furthermore, the irreversible Mn-based byproducts are inhibited, resulting in durable cycling performance. After 2500 charge/discharge cycles, the initial capacity remains 91 %. This work provides an important strategy to utilize Mn<sup>2+</sup> efficiently and develop a robust Mn-based cathode, which could greatly prompt the practical application of aqueous zinc ion batteries.</div></div>\",\"PeriodicalId\":306,\"journal\":{\"name\":\"Energy Storage Materials\",\"volume\":\"74 \",\"pages\":\"Article 103887\"},\"PeriodicalIF\":18.9000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Storage Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S240582972400713X\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S240582972400713X","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

摘要

锰基氧化物阴极的溶解是一个亟待解决的问题,因为它会导致电化学不可逆的副产品,最终导致电池失效。在这项研究中,我们提出将具有 H 空位的活化镍锰-LDHv 纳米片作为耐用锌离子电池的阴极材料。H 空位通过重新分配电子密度和建立强 Mn-O 键来促进 Mn2+ 的沉积,从而使 NiMn-LDHv 具有可控的 Mn2+ 反沉积能力。实验验证了 MnO2 在充电过程中沉积在镍锰-LHDv 衬底上,MnO2 的溶解和 Zn2+/H+ 共掺杂对放电容量有综合贡献。采用镍锰-LDHv 正极的全电池在 0.3 A g-1 时的速率容量为 258 mAh g-1,在 11.0 A g-1 时的速率容量甚至达到 90 mAh g-1。此外,还抑制了不可逆的锰基副产物,从而实现了持久的循环性能。经过 2500 次充放电循环后,初始容量仍保持在 91%。这项研究为高效利用 Mn2+ 和开发坚固的锰基阴极提供了重要策略,这将极大地促进锌离子水电池的实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

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
Highly efficient Mn2+ deposition induced by H-vacancies of NiMn-LDH nanosheets for durable zinc ion batteries
The dissolution of Mn-based oxides cathodes is an urgent issue, as it leads to electrochemically irreversible byproducts and, finally, battery failure. In this work, activated NiMn-LDHv nanosheets with H vacancies are proposed as the cathode material for durable zinc ion batteries. The H vacancies promote Mn2+ deposition by redistributing the electron density and building strong Mn-O bonds, as a result, endowing NiMn-LDHv with the ability of controllable back-deposition of Mn2+. It's verified that MnO2 is deposited on the NiMn-LHDv substrate during charging, the dissolution and the Zn2+/H+ co-intercalation of MnO2 have a combined contribution to the discharge capacity. The full battery with NiMn-LDHv cathode delivers rate capacity of 258 mAh g−1 at 0.3 A g−1, and even 90 mAh g−1 at 11.0 A g−1. Furthermore, the irreversible Mn-based byproducts are inhibited, resulting in durable cycling performance. After 2500 charge/discharge cycles, the initial capacity remains 91 %. This work provides an important strategy to utilize Mn2+ efficiently and develop a robust Mn-based cathode, which could greatly prompt the practical application of aqueous zinc ion batteries.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Energy Storage Materials
Energy Storage Materials Materials Science-General Materials Science
CiteScore
33.00
自引率
5.90%
发文量
652
审稿时长
27 days
期刊介绍: Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field. Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy. Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.
期刊最新文献
Optimized molecular interactions significantly enhance capacitive energy storage in polymer blends at 150 °C A High Power Flexible Zn-Air Battery via Concurrent PAA Modulation and Structural Tuning Surface acidity regulation for boosting Li2O2 decomposition towards lower charge overpotential Li–O2 batteries “Preferential Adsorption-Decomposition and Strong Binding” Strategy-Derived Interphase Enabling Fast-Charging and Wide-Temperature Sodium Metal Batteries Unlocking Advanced Sodium Storage Performance: High-Entropy Modulates Crystallographic Sites with Reversible Multi-Electron Reaction
×
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