In3+-doped BiVO4 film photoanodes with passivated surface states for efficient photoelectrochemical water oxidation.

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Using the electrochemical CO 2 reduction reaction (CO 2 RR) with Cu-based electrocatalysts to achieve carbonneutral cycles remains a significant challenge because of its low selectivity and poor stability. Modulating the surface electron distribution by defects engineering or doping can effectively improve CO 2 RR performance. Herein, we synthesize the electrocatalyst of V o -CuO(Sn) nanosheets containing oxygen vacancies and Sn dopants for application in CO 2 RR-to-CO. Density functional theory calculations confirm that the incorporation of oxygen vacancies and Sn atoms substantially reduces the energy barrier for *COOH and *CO intermediate formation, which results in the high efficiency, low overpotential, and superior stability of the CO 2 RR to CO conversion. This electrocatalyst possesses a high Faraday efficiency (FE) of 99.9% for CO at a low overpotential of 420 mV and a partial current density of up to 35.22 mA cm −2 at −1.03 V versus reversible hydrogen electrode (RHE). The FE CO of V o -CuO(Sn) could retain over 95% within a wide potential area from −0.48 to −0.93 V versus RHE. Moreover, we obtain long-term stability for more than 180 h with only a slight decay in its activity. Therefore, this work provides an effective route for designing environmentally friendly electrocatalysts to improve the selectivity and stability of the CO 2 RR to CO conversion.

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