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Abstract Metal oxides are archetypal CO 2 reduction reaction electrocatalysts, yet inevitable self-reduction will enhance competitive hydrogen evolution and lower the CO 2 electroreduction selectivity. Herein, we propose a tangible superlattice model of alternating metal oxides and selenide sublayers in which electrons are rapidly exported through the conductive metal selenide layer to protect the active oxide layer from self-reduction. Taking BiCuSeO superlattices as a proof-of-concept, a comprehensive characterization reveals that the active Bi 2 O 2 2+ sublayers retain oxidation states rather than their self-reduced Bi metal during CO 2 electroreduction because of the rapid electron transfer through the conductive Cu 2 Se 2 2- sublayer. Theoretical calculations uncover the high activity over Bi 2 O 2 2+ sublayers due to the overlaps between the Bi p orbitals and O p orbitals in the OCHO* intermediate, thus achieving over 90% formate selectivity in a wide potential range from −0.4 to −1.1 V. This work broadens the studying and improving of the CO 2 electroreduction properties of metal oxide systems.
Duan et al. (Tue,) studied this question.
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