{"title":"High density facet junctions in nano-stepped CuFeO2 enable efficient charge separation for selective photocatalytic CO2 reduction to CH4","authors":"Jingying Wei, Chun Guo, Dongfen Hou, Dailing Jia, Huaiguo Xue, Jingqi Tian, Tengfei Jiang","doi":"10.1039/d5qi00055f","DOIUrl":null,"url":null,"abstract":"Facet junctions have been demonstrated to be effective in promoting the separation of photoinduced charges. However, the micro-size of photocatalysts with a limited density of facet junctions usually hinders the improvement of photocatalytic performance. In this work, we propose the synthesis of nanoscale CuFeO<small><sub>2</sub></small> through a hydrothermal and acid etching strategy, which leads to the formation of stepped CuFeO<small><sub>2</sub></small> hexagonal nanosheets with high-density facet junctions. Experimental characterization and density functional theory (DFT) calculations indicate that the steps are composed of horizontal (001) and vertical (−120) facets that form facet junctions, between which a work function difference of 0.74 eV induces the formation of a built-in electric field. Surface photovoltage measurements further demonstrate directional photoinduced electron transfer from (−120) to (001) to generate an electron-rich surface in CuFeO<small><sub>2</sub></small>. As a result, the stepped CuFeO<small><sub>2</sub></small> with high-density facet junctions exhibits superior photocatalytic performance in the reduction of CO<small><sub>2</sub></small> to CH<small><sub>4</sub></small> compared to non-stepped CuFeO<small><sub>2</sub></small>, with a rate of 43.79 μmol g<small><sup>−1</sup></small> h<small><sup>−1</sup></small> and 78% selectivity. <em>In situ</em> infrared spectroscopy further reveals that the stepped CuFeO<small><sub>2</sub></small> with a high density of facet junctions is more conducive to the formation of key CH<small><sub>3</sub></small>O* intermediates that promote CH<small><sub>4</sub></small> production.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"16 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi00055f","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
Abstract
Facet junctions have been demonstrated to be effective in promoting the separation of photoinduced charges. However, the micro-size of photocatalysts with a limited density of facet junctions usually hinders the improvement of photocatalytic performance. In this work, we propose the synthesis of nanoscale CuFeO2 through a hydrothermal and acid etching strategy, which leads to the formation of stepped CuFeO2 hexagonal nanosheets with high-density facet junctions. Experimental characterization and density functional theory (DFT) calculations indicate that the steps are composed of horizontal (001) and vertical (−120) facets that form facet junctions, between which a work function difference of 0.74 eV induces the formation of a built-in electric field. Surface photovoltage measurements further demonstrate directional photoinduced electron transfer from (−120) to (001) to generate an electron-rich surface in CuFeO2. As a result, the stepped CuFeO2 with high-density facet junctions exhibits superior photocatalytic performance in the reduction of CO2 to CH4 compared to non-stepped CuFeO2, with a rate of 43.79 μmol g−1 h−1 and 78% selectivity. In situ infrared spectroscopy further reveals that the stepped CuFeO2 with a high density of facet junctions is more conducive to the formation of key CH3O* intermediates that promote CH4 production.