High density facet junctions in nano-stepped CuFeO2 enable efficient charge separation for selective photocatalytic CO2 reduction to CH4

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.

Graphical abstract: High density facet junctions in nano-stepped CuFeO2 enable efficient charge separation for selective photocatalytic CO2 reduction to CH4

Supplementary files

Article information

Article type
Research Article
Submitted
07 Jan 2025
Accepted
14 Mar 2025
First published
24 Mar 2025

Inorg. Chem. Front., 2025, Advance Article

High density facet junctions in nano-stepped CuFeO2 enable efficient charge separation for selective photocatalytic CO2 reduction to CH4

J. Wei, C. Guo, D. Hou, D. Jia, H. Xue, J. Tian and T. Jiang, Inorg. Chem. Front., 2025, Advance Article , DOI: 10.1039/D5QI00055F

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