Abstract

Modulating the electronic properties of transition metal sites in photocatalysts at the atomic level is essential for achieving high-activity carbon dioxide photoreduction (CO2PR). An electronic strategy is herein proposed to engineer In-d-band center of InVO4 by incorporating MnOx nanoparticles and oxygen vacancies (VO) into holey InVO4 nanobelts (MnOx/VO-InVO4), which synergistically modulates the In-d-band center to a moderate level and consequently leads to high-efficiency CO2PR. The MnOx/VO-InVO4 catalyst with optimized electronic property exhibits a single carbon evolution rate of up to 145.3µmol g-1 h-1 and a carbon monoxide (CO) product selectivity of 92.6%, coming out in front of reported InVO4-based materials. It is discovered that the modulated electronic property favors the interaction between the In sites and their intermediates, which thereby improves the thermodynamics and kinetics of the CO2PR-to-CO reaction. This work not only demonstrates the effective engineering of the d orbital of the low-coordination In atoms to promote CO2PR, but also paves the way for the application of tuning d-band center to develop high-efficiency catalysts.

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