Tailoring Water-in-DMSO Electrolyte for Ultra-stable Rechargeable Zinc Batteries

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-01-13 DOI:10.1002/anie.202423302
Huaizheng Ren, Sai Li, Liang Xu, Lei Wang, Xinxin Liu, Lei Wang, Yue Liu, Prof. Liang Zhang, Han Zhang, Yuxin Gong, Prof. Chade Lv, Dongping Chen, Jianxin Wang, Qiang Lv, Yaqiang Li, Prof. Huakun Liu, Prof. Dianlong Wang, Prof. Tao Cheng, Prof. Bo Wang, Prof. Dongliang Chao, Prof. Shixue Dou
{"title":"Tailoring Water-in-DMSO Electrolyte for Ultra-stable Rechargeable Zinc Batteries","authors":"Huaizheng Ren,&nbsp;Sai Li,&nbsp;Liang Xu,&nbsp;Lei Wang,&nbsp;Xinxin Liu,&nbsp;Lei Wang,&nbsp;Yue Liu,&nbsp;Prof. Liang Zhang,&nbsp;Han Zhang,&nbsp;Yuxin Gong,&nbsp;Prof. Chade Lv,&nbsp;Dongping Chen,&nbsp;Jianxin Wang,&nbsp;Qiang Lv,&nbsp;Yaqiang Li,&nbsp;Prof. Huakun Liu,&nbsp;Prof. Dianlong Wang,&nbsp;Prof. Tao Cheng,&nbsp;Prof. Bo Wang,&nbsp;Prof. Dongliang Chao,&nbsp;Prof. Shixue Dou","doi":"10.1002/anie.202423302","DOIUrl":null,"url":null,"abstract":"<p>Rechargeable zinc batteries (RZBs) are hindered by two primary challenges: instability of Zn anode and deterioration of the cathode structure in traditional aqueous electrolytes, largely attributable to the decomposition of active H<sub>2</sub>O. Here, we design and synthesize a non-flammable water-in-dimethyl sulfoxide electrolyte to address these issues. X-ray absorption spectroscopy, in situ techniques and computational simulations demonstrate that the activity of H<sub>2</sub>O in this electrolyte is extremely compressed, which not only suppresses the side reactions and increases the reversibility of Zn anode, but also diminishes the cathode dissolution and proton intercalation. The hybrid solid-electrolyte interface (SEI), formed in situ, helps Zn−Zn symmetric cell a prolonged lifespan exceeding 10000 h at 0.5 mA cm<sup>−2</sup> and 600 h at a 60 % discharge depth. The versatility of this electrolyte endows the Zn-VO<sub>2</sub> full batteries ultra-stable cycling performance. This work provides insights into electrolyte structure–property relationships, and facilitates the design of high-performance RZBs.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 13","pages":""},"PeriodicalIF":16.9000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202423302","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Rechargeable zinc batteries (RZBs) are hindered by two primary challenges: instability of Zn anode and deterioration of the cathode structure in traditional aqueous electrolytes, largely attributable to the decomposition of active H2O. Here, we design and synthesize a non-flammable water-in-dimethyl sulfoxide electrolyte to address these issues. X-ray absorption spectroscopy, in situ techniques and computational simulations demonstrate that the activity of H2O in this electrolyte is extremely compressed, which not only suppresses the side reactions and increases the reversibility of Zn anode, but also diminishes the cathode dissolution and proton intercalation. The hybrid solid-electrolyte interface (SEI), formed in situ, helps Zn−Zn symmetric cell a prolonged lifespan exceeding 10000 h at 0.5 mA cm−2 and 600 h at a 60 % discharge depth. The versatility of this electrolyte endows the Zn-VO2 full batteries ultra-stable cycling performance. This work provides insights into electrolyte structure–property relationships, and facilitates the design of high-performance RZBs.

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
定制用于超稳定可充电锌电池的dmso水电解质
可充电锌电池(rzb)面临两个主要挑战:锌阳极的不稳定性和传统水溶液中锌阴极结构的恶化,这在很大程度上归因于活性水的分解。在这里,我们设计并合成了一种不易燃的二甲基亚砜水电解质来解决这些问题。x射线吸收光谱、原位技术和计算模拟表明,该电解质中H2O的活性被极大地压缩,这不仅抑制了副反应,提高了Zn阳极的可逆性,而且减少了阴极溶解和质子插层。原位形成的混合固体电解质界面(SEI)有助于延长Zn-Zn对称电池的使用寿命,在0.5 mA cm - 2下超过10000小时,在60%放电深度下超过600小时。这种电解质的多功能性赋予了锌- vo2全电池超稳定的循环性能。这项工作为电解质的结构-性能关系提供了见解,并为高性能rzb的设计提供了便利。
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
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
期刊最新文献
Programmable Morphing DNA Nanodevice Enables Triple Signal Amplification for Long-Term Early Tumor Metastasis Imaging. Discovery of Perilloxazole Pseudo-Natural Products Yields a New Sterol Biosynthesis Inhibitor Chemotype. Transforming Interfacial Reactivity Into Stability for Durable High-Current Solid-State Sodium Batteries. From [NHC─H]• to Persistent σ-Complex Radicals: Photoinduced Radical Chemistry of Imidazolium Salts. Programmable Chimeric Antigen Receptor T Cell Circuits With DNA Computing for Precision Tumor Therapy.
×
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