{"title":"多功能冠醚添加剂调节脱溶过程,实现高可逆锌金属电池","authors":"Aohua Wu, Shaojie Zhang, Qiaohui Li, Wenxian Xue, Chuanyang Li, Baojuan Xi, Wutao Mao, Keyan Bao, Shenglin Xiong","doi":"10.1002/aenm.202404450","DOIUrl":null,"url":null,"abstract":"Aqueous zinc‐ion batteries have garnered significant attention due to their abundant materials, low production costs, and safety. However, these batteries suffer from severe side reactions, which are closely associated with the presence of a substantial amount of solvent at the electrode surfaces. Herein, 1,4,7,10,13,16‐hexaoxacyclooctadecane (18‐crown‐6) is added to the electrolyte to illustrate both theoretically and experimentally its contribution to the rapid desolvation aspect. It is shown that the addition of 18‐crown‐6 to the electrolyte greatly facilitates the desolvation of the solvated structure and prevents the collection of solvent molecules on the surface of zinc anode, thus inhibiting the hydrogen precipitation reaction. It also enhances the transference number of zinc ions, which makes the interfacial electric field on the zinc anode stable and thus promotes the orderly diffusion and uniform nucleation of Zn<jats:sup>2+</jats:sup>, and inhibits the growth of dendrites. As a result, the electrolyte containing 18‐crown‐6 as additives shows a stable cycle life, Zn||Zn symmetric cell is cycled for nearly 1700 h at 1 mA cm<jats:sup>−2</jats:sup>, showing a significant improvement in Coulombic efficiency. The assembled Zn||NH<jats:sub>4</jats:sub>V<jats:sub>4</jats:sub>O<jats:sub>10</jats:sub> cell exhibits excellent electrochemical performance, reaching a capacity of 100.9 mAh g<jats:sup>−1</jats:sup> even after 4000 cycles at 10.0 A g<jats:sup>−1</jats:sup>.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"35 1","pages":""},"PeriodicalIF":24.4000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multifunctional Crown Ether Additive Regulates Desolvation Process to Achieve Highly Reversible Zinc‐Metal Batteries\",\"authors\":\"Aohua Wu, Shaojie Zhang, Qiaohui Li, Wenxian Xue, Chuanyang Li, Baojuan Xi, Wutao Mao, Keyan Bao, Shenglin Xiong\",\"doi\":\"10.1002/aenm.202404450\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aqueous zinc‐ion batteries have garnered significant attention due to their abundant materials, low production costs, and safety. However, these batteries suffer from severe side reactions, which are closely associated with the presence of a substantial amount of solvent at the electrode surfaces. Herein, 1,4,7,10,13,16‐hexaoxacyclooctadecane (18‐crown‐6) is added to the electrolyte to illustrate both theoretically and experimentally its contribution to the rapid desolvation aspect. It is shown that the addition of 18‐crown‐6 to the electrolyte greatly facilitates the desolvation of the solvated structure and prevents the collection of solvent molecules on the surface of zinc anode, thus inhibiting the hydrogen precipitation reaction. It also enhances the transference number of zinc ions, which makes the interfacial electric field on the zinc anode stable and thus promotes the orderly diffusion and uniform nucleation of Zn<jats:sup>2+</jats:sup>, and inhibits the growth of dendrites. As a result, the electrolyte containing 18‐crown‐6 as additives shows a stable cycle life, Zn||Zn symmetric cell is cycled for nearly 1700 h at 1 mA cm<jats:sup>−2</jats:sup>, showing a significant improvement in Coulombic efficiency. The assembled Zn||NH<jats:sub>4</jats:sub>V<jats:sub>4</jats:sub>O<jats:sub>10</jats:sub> cell exhibits excellent electrochemical performance, reaching a capacity of 100.9 mAh g<jats:sup>−1</jats:sup> even after 4000 cycles at 10.0 A g<jats:sup>−1</jats:sup>.\",\"PeriodicalId\":111,\"journal\":{\"name\":\"Advanced Energy Materials\",\"volume\":\"35 1\",\"pages\":\"\"},\"PeriodicalIF\":24.4000,\"publicationDate\":\"2025-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Energy Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/aenm.202404450\",\"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":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202404450","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
水性锌离子电池因其材料丰富、生产成本低、安全性好而备受关注。然而,这些电池遭受严重的副反应,这与电极表面存在大量溶剂密切相关。本文将1,4,7,10,13,16‐六氧六环十六烷(18‐crown‐6)添加到电解质中,以从理论上和实验上说明其对快速脱溶方面的贡献。结果表明,在电解液中加入18‐crown‐6,可以极大地促进溶剂化结构的脱溶,防止溶剂分子在锌阳极表面聚集,从而抑制氢的析出反应。它还增强了锌离子的转移数,使锌阳极上的界面电场稳定,从而促进了Zn2+的有序扩散和均匀成核,抑制了枝晶的生长。结果表明,含有18‐crown‐6的电解质具有稳定的循环寿命,Zn||Zn对称电池在1 mA cm−2下循环近1700 h,库仑效率显著提高。组装的Zn||NH4V4O10电池表现出优异的电化学性能,在10.0 a g−1下循环4000次后,电池容量达到100.9 mAh g−1。
Multifunctional Crown Ether Additive Regulates Desolvation Process to Achieve Highly Reversible Zinc‐Metal Batteries
Aqueous zinc‐ion batteries have garnered significant attention due to their abundant materials, low production costs, and safety. However, these batteries suffer from severe side reactions, which are closely associated with the presence of a substantial amount of solvent at the electrode surfaces. Herein, 1,4,7,10,13,16‐hexaoxacyclooctadecane (18‐crown‐6) is added to the electrolyte to illustrate both theoretically and experimentally its contribution to the rapid desolvation aspect. It is shown that the addition of 18‐crown‐6 to the electrolyte greatly facilitates the desolvation of the solvated structure and prevents the collection of solvent molecules on the surface of zinc anode, thus inhibiting the hydrogen precipitation reaction. It also enhances the transference number of zinc ions, which makes the interfacial electric field on the zinc anode stable and thus promotes the orderly diffusion and uniform nucleation of Zn2+, and inhibits the growth of dendrites. As a result, the electrolyte containing 18‐crown‐6 as additives shows a stable cycle life, Zn||Zn symmetric cell is cycled for nearly 1700 h at 1 mA cm−2, showing a significant improvement in Coulombic efficiency. The assembled Zn||NH4V4O10 cell exhibits excellent electrochemical performance, reaching a capacity of 100.9 mAh g−1 even after 4000 cycles at 10.0 A g−1.
期刊介绍:
Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small.
With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics.
The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.