通过重构 M(OH)x/Fe3O4 催化剂促进氧气进化反应

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2024-08-06 DOI:10.1039/D4QI01574F
Xiaoqu Wang, Limin Wang, Yongchun Liu, Rajkumar Devasenathipathy, Li Liu, Qiulan Huang, Dujuan Huang, Youjun Fan, Du-Hong Chen and Wei Chen
{"title":"通过重构 M(OH)x/Fe3O4 催化剂促进氧气进化反应","authors":"Xiaoqu Wang, Limin Wang, Yongchun Liu, Rajkumar Devasenathipathy, Li Liu, Qiulan Huang, Dujuan Huang, Youjun Fan, Du-Hong Chen and Wei Chen","doi":"10.1039/D4QI01574F","DOIUrl":null,"url":null,"abstract":"<p >For large-scale hydrogen production from electrocatalysis of water, Ni- and/or Fe-based catalysts were commonly used but were limited by the ultrahigh overpotential and poor stability at a high current density (&gt;500 mA cm<small><sup>−2</sup></small>). Here, the reconstruction of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small> (M = Ni, Fe) arrays has been performed for boosting the oxygen evolution reaction (OER). The prepared M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small> grown on iron foam (M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF) catalysts exhibited low overpotentials of 214 and 311 mV for the OER at current densities of 50 and 500 mA cm<small><sup>−2</sup></small>, respectively. In addition, an excellent stability up to 70 h of operation was achieved at a current density of 10 mA cm<small><sup>−2</sup></small> in 1 M KOH. The <em>in situ</em> Raman spectra revealed that the reconstruction of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF boosted the OER activity. Theoretical calculations revealed favorable absorption of O<small><sub>2</sub></small> at the Ni site of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF during the OER. This work highlights the reconstruction of structurally definite catalysts for promoting the catalytic activity toward the OER and the large-scale electrocatalysis of water.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":null,"pages":null},"PeriodicalIF":6.1000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosting the oxygen evolution reaction via the reconstruction of an M(OH)x/Fe3O4 catalyst†\",\"authors\":\"Xiaoqu Wang, Limin Wang, Yongchun Liu, Rajkumar Devasenathipathy, Li Liu, Qiulan Huang, Dujuan Huang, Youjun Fan, Du-Hong Chen and Wei Chen\",\"doi\":\"10.1039/D4QI01574F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >For large-scale hydrogen production from electrocatalysis of water, Ni- and/or Fe-based catalysts were commonly used but were limited by the ultrahigh overpotential and poor stability at a high current density (&gt;500 mA cm<small><sup>−2</sup></small>). Here, the reconstruction of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small> (M = Ni, Fe) arrays has been performed for boosting the oxygen evolution reaction (OER). The prepared M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small> grown on iron foam (M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF) catalysts exhibited low overpotentials of 214 and 311 mV for the OER at current densities of 50 and 500 mA cm<small><sup>−2</sup></small>, respectively. In addition, an excellent stability up to 70 h of operation was achieved at a current density of 10 mA cm<small><sup>−2</sup></small> in 1 M KOH. The <em>in situ</em> Raman spectra revealed that the reconstruction of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF boosted the OER activity. Theoretical calculations revealed favorable absorption of O<small><sub>2</sub></small> at the Ni site of M(OH)<small><sub><em>x</em></sub></small>/Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>/IF during the OER. This work highlights the reconstruction of structurally definite catalysts for promoting the catalytic activity toward the OER and the large-scale electrocatalysis of water.</p>\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2024-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi01574f\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi01574f","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

在水的电催化大规模制氢过程中,通常使用镍基和/或铁基催化剂,但这些催化剂在高电流密度(500 mA cm-2)下具有超高过电位和稳定性差的缺点。在此,我们制备了重构的 M(OH)x/Fe3O4(M = Ni、Fe)阵列,用于促进氧进化反应(OER)。所制备的 M(OH)x/Fe3O4 长在泡沫铁上(M(OH)x/Fe3O4/IF)催化剂在 50 mA cm-2 和 500 mA cm-2 的电流密度下,OER 的过电位分别为 214 mV 和 311 mV。原位拉曼光谱显示,M(OH)x/Fe3O4/IF 的重构提高了 OER 的活性。理论计算显示,在 OER 过程中,M(OH)x/Fe3O4/IF 的 Ni 位点有利于吸收 O2。这项工作强调了重构结构明确的催化剂对提高 OER 催化活性和大规模水电催化的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Boosting the oxygen evolution reaction via the reconstruction of an M(OH)x/Fe3O4 catalyst†

For large-scale hydrogen production from electrocatalysis of water, Ni- and/or Fe-based catalysts were commonly used but were limited by the ultrahigh overpotential and poor stability at a high current density (>500 mA cm−2). Here, the reconstruction of M(OH)x/Fe3O4 (M = Ni, Fe) arrays has been performed for boosting the oxygen evolution reaction (OER). The prepared M(OH)x/Fe3O4 grown on iron foam (M(OH)x/Fe3O4/IF) catalysts exhibited low overpotentials of 214 and 311 mV for the OER at current densities of 50 and 500 mA cm−2, respectively. In addition, an excellent stability up to 70 h of operation was achieved at a current density of 10 mA cm−2 in 1 M KOH. The in situ Raman spectra revealed that the reconstruction of M(OH)x/Fe3O4/IF boosted the OER activity. Theoretical calculations revealed favorable absorption of O2 at the Ni site of M(OH)x/Fe3O4/IF during the OER. This work highlights the reconstruction of structurally definite catalysts for promoting the catalytic activity toward the OER and the large-scale electrocatalysis of water.

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
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
期刊最新文献
Hierarchical FeCo LDH/NiSe heterostructure electrocatalysts with rich heterointerfaces for robust water splitting at industrial-level current density Ultrathin 2D NiCo-MOF bimetallic nanosheets as single-atom catalysts for chemoselective hydrogenation of nitroarenes Naphthalene diimide-based crystalline hybrid photochromic materials: Structural types, photochromic mechanism, and applications Ionic-liquid/metal-organic-framework composites: Synthesis and emerging sustainable applications Back cover
×
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