以强代弱:氢键锚定电解质实现超稳定和宽温水性锌离子电容器

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-11-11 DOI:10.1002/anie.202418242
Zhongyou Peng, Ling Tang, Shulong Li, Licheng Tan, Yiwang Chen
{"title":"以强代弱:氢键锚定电解质实现超稳定和宽温水性锌离子电容器","authors":"Zhongyou Peng, Ling Tang, Shulong Li, Licheng Tan, Yiwang Chen","doi":"10.1002/anie.202418242","DOIUrl":null,"url":null,"abstract":"Despite aqueous electrolytes offer a great opportunity for large-scale energy storage owing to their safety and cost-effectiveness, their practical application suffers from the parasitic side reactions and poor temperature adaptability stemming from weak hydrogen-bond (HB) network in free water. Here, we propose the guiding thought “strong replaces weak” to design hydrogen bond-anchored electrolyte by introducing sulfolane (SL) for disrupting the regular weak HB network and contributing to superior temperature tolerance. Judiciously combined experimental characterization and theoretical calculation confirm that SL can remodel the primary solvation shell of metal ions, customize stable electrode interface chemistry and restrain the side reactions. Consequently, symmetric supercapacitor constructed by activated carbon (AC) electrodes is able to fully work within a voltage range of 2.4 V and reach high capacitance retention of 89.8% after 60000 cycles. Additionally, Zn anodes exhibit ultra-stable Zn plating/stripping behaviors and a wide temperature range (-20 ~ 60 °C), and zinc-ion capacitor (Zn//AC) also delivers an excellent cycling stability with capacity retention of 99.7% after 55000 cycles, implying that the designed electrolyte has practical application potential in extreme environments. This work proposes a novel critical solvation strategy that paves the route for the construction of ultra-stable and wide-temperature aqueous energy storage devices.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":null,"pages":null},"PeriodicalIF":16.1000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Strong Replaces Weak: ​Hydrogen Bond-Anchored Electrolyte Enabling Ultra-Stable and Wide-Temperature Aqueous Zinc-Ion Capacitors\",\"authors\":\"Zhongyou Peng, Ling Tang, Shulong Li, Licheng Tan, Yiwang Chen\",\"doi\":\"10.1002/anie.202418242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Despite aqueous electrolytes offer a great opportunity for large-scale energy storage owing to their safety and cost-effectiveness, their practical application suffers from the parasitic side reactions and poor temperature adaptability stemming from weak hydrogen-bond (HB) network in free water. Here, we propose the guiding thought “strong replaces weak” to design hydrogen bond-anchored electrolyte by introducing sulfolane (SL) for disrupting the regular weak HB network and contributing to superior temperature tolerance. Judiciously combined experimental characterization and theoretical calculation confirm that SL can remodel the primary solvation shell of metal ions, customize stable electrode interface chemistry and restrain the side reactions. Consequently, symmetric supercapacitor constructed by activated carbon (AC) electrodes is able to fully work within a voltage range of 2.4 V and reach high capacitance retention of 89.8% after 60000 cycles. Additionally, Zn anodes exhibit ultra-stable Zn plating/stripping behaviors and a wide temperature range (-20 ~ 60 °C), and zinc-ion capacitor (Zn//AC) also delivers an excellent cycling stability with capacity retention of 99.7% after 55000 cycles, implying that the designed electrolyte has practical application potential in extreme environments. This work proposes a novel critical solvation strategy that paves the route for the construction of ultra-stable and wide-temperature aqueous energy storage devices.\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2024-11-11\",\"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://doi.org/10.1002/anie.202418242\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202418242","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

摘要

尽管水基电解质因其安全性和成本效益而为大规模储能提供了巨大的机遇,但其实际应用却受到自由水中弱氢键(HB)网络所产生的寄生副反应和温度适应性差的影响。在此,我们提出了 "以强补弱 "的指导思想,通过引入羟基磺烷(SL)来设计氢键锚定电解质,从而打破常规的弱氢键网络,提高温度耐受性。实验表征与理论计算相结合的结果证实,SL 可以重塑金属离子的主溶胶壳,定制稳定的电极界面化学性质并抑制副反应。因此,由活性炭(AC)电极构建的对称超级电容器能够在 2.4 V 的电压范围内完全工作,并在 60000 次循环后达到 89.8% 的高电容保持率。此外,锌阳极表现出超稳定的锌电镀/剥离行为和宽温度范围(-20 ~ 60 °C),锌离子电容器(Zn//AC)也具有极佳的循环稳定性,在 55000 次循环后容量保持率达 99.7%,这意味着所设计的电解质在极端环境中具有实际应用潜力。这项工作提出了一种新的临界溶解策略,为构建超稳定、宽温度水性储能器件铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Strong Replaces Weak: ​Hydrogen Bond-Anchored Electrolyte Enabling Ultra-Stable and Wide-Temperature Aqueous Zinc-Ion Capacitors
Despite aqueous electrolytes offer a great opportunity for large-scale energy storage owing to their safety and cost-effectiveness, their practical application suffers from the parasitic side reactions and poor temperature adaptability stemming from weak hydrogen-bond (HB) network in free water. Here, we propose the guiding thought “strong replaces weak” to design hydrogen bond-anchored electrolyte by introducing sulfolane (SL) for disrupting the regular weak HB network and contributing to superior temperature tolerance. Judiciously combined experimental characterization and theoretical calculation confirm that SL can remodel the primary solvation shell of metal ions, customize stable electrode interface chemistry and restrain the side reactions. Consequently, symmetric supercapacitor constructed by activated carbon (AC) electrodes is able to fully work within a voltage range of 2.4 V and reach high capacitance retention of 89.8% after 60000 cycles. Additionally, Zn anodes exhibit ultra-stable Zn plating/stripping behaviors and a wide temperature range (-20 ~ 60 °C), and zinc-ion capacitor (Zn//AC) also delivers an excellent cycling stability with capacity retention of 99.7% after 55000 cycles, implying that the designed electrolyte has practical application potential in extreme environments. This work proposes a novel critical solvation strategy that paves the route for the construction of ultra-stable and wide-temperature aqueous energy storage devices.
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
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
Organic Circularly Polarized Room‐Temperature Phosphorescence: Strategies, Applications and Challenges Bioinspired “Intermolecular Pocket” in Soft Molecular Crystal of Porous Organic Cage Exhibiting Reversible Guest Recognition Inside Front Cover: Two‐dimensional Supramolecular Polymorphism in Cyanine H‐ and J‐aggregates Heptannulated Perylene Diimides: Formation and Reactivity of Electron-Deficient Tropylium Cations and Heptafulvenes. Long-Term Single-Molecule Tracking in Living Cells Using Weak-Affinity Protein Labeling.
×
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