Gas-Phase Conversion Promising Controlled Construction of Functional ZnF2/V2CTx for Stabilizing Zn Metal Anodes Toward Aqueous Zinc-Ion Batteries

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xinyue Gao, Yang Liu, Maoqiang Shen, Xuesen Liu, Yanhao Zhao, Linrui Hou, Changzhou Yuan
{"title":"Gas-Phase Conversion Promising Controlled Construction of Functional ZnF2/V2CTx for Stabilizing Zn Metal Anodes Toward Aqueous Zinc-Ion Batteries","authors":"Xinyue Gao, Yang Liu, Maoqiang Shen, Xuesen Liu, Yanhao Zhao, Linrui Hou, Changzhou Yuan","doi":"10.1002/adfm.202503212","DOIUrl":null,"url":null,"abstract":"The practical application of aqueous zinc-ion batteries (AZIBs) is impeded by notorious side reactions occurring at the zinc anode including zinc dendrite growth, hydrogen evolution reaction and anodic corrosion. To address these issues, ZnF<sub>2</sub> combined with V<sub>2</sub>C MXene composite (ZnF<sub>2</sub>/V<sub>2</sub>CT<sub>x</sub>) is <i>in-situ</i> synthesized from V<sub>2</sub>ZnC MAX through a facile gas-phase fluorination strategy and utilized as an efficient protective coating layer for Zn anode. The ionically conductive and hydrophobic ZnF<sub>2</sub> inhibits hydrogen evolution reaction and promotes uniform distribution and migration of Zn<sup>2+</sup>. Meanwhile, the electronically conductive V<sub>2</sub>CT<sub>x</sub> effectively homogenizes the electric field and reduces local current density. Consequently, a stable, dendrite-free Zn anode with excellent cycling stability (over 2100 h at 3.0 mA cm<sup>−2</sup>) is achieved. Furthermore, ZnF<sub>2</sub>/V<sub>2</sub>CT<sub>x</sub> coating layer not only significantly improves the reversibility of zinc deposition/stripping, but efficiently reduces the electrochemical polarization. When paired with a zinc vanadate (Zn<sub>2</sub>V<sub>2</sub>O<sub>7</sub> and ZnV<sub>3</sub>O<sub>8</sub>) cathode derived directly from the gas-phase oxidation of V<sub>2</sub>ZnC, the full cells exhibit a 1000-cycle lifespan at 5.0 A g<sup>−1</sup>, and superior rate performance (≈237.6 mAh g<sup>−1</sup> at 10.0 A g<sup>−1</sup>). This work presents a novel and efficient strategy to controllably construct MAX phase derivatives for next-generation AZIBs.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"50 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202503212","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The practical application of aqueous zinc-ion batteries (AZIBs) is impeded by notorious side reactions occurring at the zinc anode including zinc dendrite growth, hydrogen evolution reaction and anodic corrosion. To address these issues, ZnF2 combined with V2C MXene composite (ZnF2/V2CTx) is in-situ synthesized from V2ZnC MAX through a facile gas-phase fluorination strategy and utilized as an efficient protective coating layer for Zn anode. The ionically conductive and hydrophobic ZnF2 inhibits hydrogen evolution reaction and promotes uniform distribution and migration of Zn2+. Meanwhile, the electronically conductive V2CTx effectively homogenizes the electric field and reduces local current density. Consequently, a stable, dendrite-free Zn anode with excellent cycling stability (over 2100 h at 3.0 mA cm−2) is achieved. Furthermore, ZnF2/V2CTx coating layer not only significantly improves the reversibility of zinc deposition/stripping, but efficiently reduces the electrochemical polarization. When paired with a zinc vanadate (Zn2V2O7 and ZnV3O8) cathode derived directly from the gas-phase oxidation of V2ZnC, the full cells exhibit a 1000-cycle lifespan at 5.0 A g−1, and superior rate performance (≈237.6 mAh g−1 at 10.0 A g−1). This work presents a novel and efficient strategy to controllably construct MAX phase derivatives for next-generation AZIBs.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信