Bio-inspired Hydrated Deep Eutectic Electrolyte Enables Long-lifespan Zinc Anode Across a Broad Temperature Range

IF 18.9 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Energy Storage Materials Pub Date : 2025-03-11 DOI:10.1016/j.ensm.2025.104174
Min Cheng, Qiong Sun, Tianjiang Sun, Mengyao Shi, Weijia Zhang, Diantao Li, Zhengtai Zha, Haixia Li, Kai Zhang, Zhanliang Tao
{"title":"Bio-inspired Hydrated Deep Eutectic Electrolyte Enables Long-lifespan Zinc Anode Across a Broad Temperature Range","authors":"Min Cheng, Qiong Sun, Tianjiang Sun, Mengyao Shi, Weijia Zhang, Diantao Li, Zhengtai Zha, Haixia Li, Kai Zhang, Zhanliang Tao","doi":"10.1016/j.ensm.2025.104174","DOIUrl":null,"url":null,"abstract":"Aqueous zinc-ion batteries (AZIBs) often suffered from parasitic side reactions associated with the active water and dendrite growth. Herein, motivated by the exceptional hydrophilic properties and the ability to act as a protective barrier for cells of ectoin (ET), a new-type hydrated eutectic electrolyte consisting of Zn(ClO<sub>4</sub>)<sub>2</sub>·6H<sub>2</sub>O, ET, and H<sub>2</sub>O in a molar ratio of 1:1:6 (ET-6) was developed for the dendrite-free zinc anodes. The H<sub>2</sub>O activity in the electrolyte was reduced by the ET-involved Zn<sup>2+</sup> solvation structure and the strong hydrogen bond between ET and H<sub>2</sub>O, thus inhibiting hydrogen evolution reaction (HER) and corrosion on the zinc anode. The regulated hydrogen bond network enables the electrolyte with an ultralow freezing point of −104.8°C. Moreover, the ET in ET-6 forms a biologically inspired interface protective layer on the surface of the zinc anode. The adsorbed ET molecules effectively capture free H<sub>2</sub>O molecules near the zinc surface and promotes the (002)-exposed stripping/plating, thereby enabling the eutectic-based electrolyte, which is plagued by dendrite problems, to achieve a dendrite-free zinc anode. Consequently, this electrolyte enables the zinc anode with long lifespan within a broad temperature range from −40°C to 50°C.","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"31 1","pages":""},"PeriodicalIF":18.9000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.ensm.2025.104174","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

Aqueous zinc-ion batteries (AZIBs) often suffered from parasitic side reactions associated with the active water and dendrite growth. Herein, motivated by the exceptional hydrophilic properties and the ability to act as a protective barrier for cells of ectoin (ET), a new-type hydrated eutectic electrolyte consisting of Zn(ClO4)2·6H2O, ET, and H2O in a molar ratio of 1:1:6 (ET-6) was developed for the dendrite-free zinc anodes. The H2O activity in the electrolyte was reduced by the ET-involved Zn2+ solvation structure and the strong hydrogen bond between ET and H2O, thus inhibiting hydrogen evolution reaction (HER) and corrosion on the zinc anode. The regulated hydrogen bond network enables the electrolyte with an ultralow freezing point of −104.8°C. Moreover, the ET in ET-6 forms a biologically inspired interface protective layer on the surface of the zinc anode. The adsorbed ET molecules effectively capture free H2O molecules near the zinc surface and promotes the (002)-exposed stripping/plating, thereby enabling the eutectic-based electrolyte, which is plagued by dendrite problems, to achieve a dendrite-free zinc anode. Consequently, this electrolyte enables the zinc anode with long lifespan within a broad temperature range from −40°C to 50°C.

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
求助全文
约1分钟内获得全文 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
Bio-inspired Hydrated Deep Eutectic Electrolyte Enables Long-lifespan Zinc Anode Across a Broad Temperature Range Li2CO3 Contamination in Garnet Solid Electrolyte: Origins, Impacts, and Mitigation Strategies Leveraging High-Entropy Substitution to Achieve V4+/V5+ Redox Couple and Superior Na+ Storage in Na3V2(PO4)3-based Cathodes for Sodium-Ion Battery From Li7La3Zr2O12 to Li4La4Zr2Cl24: Rapid three-dimensional transport of ions in halide solid electrolytes Size- and Crystallinity-dependent Oxygen Vacancy Engineering to Modulate Fe Active Sites for Enhanced Reversible Nitrogen Fixation in Lithium-nitrogen Batteries
×
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