{"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 (>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 (>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。
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.