Unlocking bimetallic active sites via a desalination strategy for photocatalytic reduction of atmospheric carbon dioxide

Ultrathin two-dimensional (2D) metal oxyhalides exhibit outstanding photocatalytic properties with unique electronic and interfacial structures. Compared with monometallic oxyhalides, bimetallic oxyhalides are less explored. In this work, we have developed a novel top-down wet-chemistry desalination approach to remove the alkali-halide salt layer within the complicated precursor bulk structural matrix Pb 0.6 Bi 1.4 Cs 0.6 O 2 Cl 2 , and successfully fabricate a new 2D ultrathin bimetallic oxyhalide Pb 0.6 Bi 1.4 O 2 Cl 1.4 . The unlocked larger surface area, rich bimetallic active sites, and faster carrier dynamics within Pb 0.6 Bi 1.4 O 2 Cl 1.4 layers significantly enhance the photocatalytic efficiency for atmospheric CO 2 reduction. It outperforms the corresponding parental matrix phase and other state-of-the-art bismuth-based monometallic oxyhalides photocatalysts. This work reports a top-down desalination strategy to engineering ultrathin bimetallic 2D material for photocatalytic atmospheric CO 2 reduction, which sheds light on further constructing other ultrathin 2D catalysts for environmental and energy applications from similar complicate structure matrixes.