Efficient synthesis of nano high-entropy compounds for advanced oxygen evolution reaction

IF 8.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chinese Chemical Letters Pub Date : 2024-09-24 DOI:10.1016/j.cclet.2024.110498
Genxiang Wang , Linfeng Fan , Peng Wang , Junfeng Wang , Fen Qiao , Zhenhai Wen
{"title":"Efficient synthesis of nano high-entropy compounds for advanced oxygen evolution reaction","authors":"Genxiang Wang ,&nbsp;Linfeng Fan ,&nbsp;Peng Wang ,&nbsp;Junfeng Wang ,&nbsp;Fen Qiao ,&nbsp;Zhenhai Wen","doi":"10.1016/j.cclet.2024.110498","DOIUrl":null,"url":null,"abstract":"<div><div>Developing efficient electrocatalysts for oxygen evolution reaction (OER) is imperative to enhance the overall efficiency of electrolysis systems and rechargeable metal-air batteries operating in aqueous solutions. High-entropy materials, featured with their distinctive multi-component properties, have found extensive application as catalysts in electrochemical energy storage and conversion devices. However, synthesizing nanostructured high-entropy compounds under mild conditions poses a significant challenge due to the difficulty in overcoming the immiscibility of multiple metallic constituents. In this context, the current study focuses on the synthesis of an array of nano-sized high entropy sulfides tailored for OER <em>via</em> a facile precursor pyrolysis method at low temperature. The representative compound, FeCoNiCuMnS<sub>x</sub>, demonstrates remarkable OER performance, achieving a current density of 10 mA/cm<sup>2</sup> at an overpotential of merely 220 mV and excellent stability with constant electrolysis at 100 mA/cm<sup>2</sup> for over 400 h. The <em>in-situ</em> formed metal (oxy)hydroxide has been confirmed as the real active sites and its exceptional performance can be primarily attributed to the synergistic effects arising from its multiple components. Furthermore, the synthetic methodology presented here is versatile and can be extended to the preparation of high entropy phosphides, which also present favorable OER performance. This research not only introduces promising non-noble electrocatalysts for OER but also offers a facile approach to expand the family of nano high-entropy materials, contributing significantly to the field of electrochemical energy conversion.</div></div>","PeriodicalId":10088,"journal":{"name":"Chinese Chemical Letters","volume":"36 4","pages":"Article 110498"},"PeriodicalIF":8.9000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Chemical Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1001841724010179","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

Developing efficient electrocatalysts for oxygen evolution reaction (OER) is imperative to enhance the overall efficiency of electrolysis systems and rechargeable metal-air batteries operating in aqueous solutions. High-entropy materials, featured with their distinctive multi-component properties, have found extensive application as catalysts in electrochemical energy storage and conversion devices. However, synthesizing nanostructured high-entropy compounds under mild conditions poses a significant challenge due to the difficulty in overcoming the immiscibility of multiple metallic constituents. In this context, the current study focuses on the synthesis of an array of nano-sized high entropy sulfides tailored for OER via a facile precursor pyrolysis method at low temperature. The representative compound, FeCoNiCuMnSx, demonstrates remarkable OER performance, achieving a current density of 10 mA/cm2 at an overpotential of merely 220 mV and excellent stability with constant electrolysis at 100 mA/cm2 for over 400 h. The in-situ formed metal (oxy)hydroxide has been confirmed as the real active sites and its exceptional performance can be primarily attributed to the synergistic effects arising from its multiple components. Furthermore, the synthetic methodology presented here is versatile and can be extended to the preparation of high entropy phosphides, which also present favorable OER performance. This research not only introduces promising non-noble electrocatalysts for OER but also offers a facile approach to expand the family of nano high-entropy materials, contributing significantly to the field of electrochemical energy conversion.

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
先进析氧反应中纳米高熵化合物的高效合成
开发高效的析氧反应电催化剂是提高电解系统和水溶液中可充电金属-空气电池整体效率的必要条件。高熵材料以其独特的多组分特性在电化学储能和转换装置中作为催化剂得到了广泛的应用。然而,在温和条件下合成纳米结构的高熵化合物由于难以克服多种金属成分的不混溶性而面临重大挑战。在此背景下,目前的研究重点是通过低温易前驱体热解方法合成一系列适合OER的纳米级高熵硫化物。代表性化合物FeCoNiCuMnSx表现出卓越的OER性能,在过电位仅为220 mV时电流密度达到10 mA/cm2,并且在100 mA/cm2恒定电解超过400 h时具有优异的稳定性。原位形成的金属(氧)氢氧化物已被确认为真正的活性位点,其优异的性能主要归因于其多种组分产生的协同效应。此外,本文提出的合成方法是通用的,可以扩展到制备高熵磷化物,这也具有良好的OER性能。该研究不仅为OER提供了有前途的非贵金属电催化剂,而且为扩大纳米高熵材料家族提供了一种简便的方法,对电化学能量转换领域做出了重大贡献。
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
Chinese Chemical Letters
Chinese Chemical Letters 化学-化学综合
CiteScore
14.10
自引率
15.40%
发文量
8969
审稿时长
1.6 months
期刊介绍: Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.
期刊最新文献
Graphical Abstracts IFC - Editorial Board/ Publication info Graphical Abstracts IFC - Editorial Board/ Publication info Synergistic homogeneous photochemical and halogen-bond catalysis toward antitumor sulfonylated fused (hetero)arenes
×
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: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