Photocatalytic CO2 reduction of Ag/Ag2S/Ti3C2T X heterojunctions with enhanced interfacial charge transfer.

Photocatalytic reduction of CO₂ to produce organic fuels is a promising strategy for addressing carbon reduction and energy scarcity. Transition metal carbides (Ti₃C₂T _X ) are of particular interest due to their unique layered structures and excellent electrical conductivity. However, the practical application of Ti₃C₂T _X is limited by the poor separation efficiency of photogenerated charge carriers and the low migration ability of photogenerated electrons. Herein, Ag/Ag₂S/Ti₃C₂T _X heterojunctions were synthesized by depositing Ag/Ag₂S nanoparticles onto layered Ti₃C₂T _X substrates using a combination of co-precipitation and photoreduction methods. Fluorescence spectra, UV diffuse reflection, and photoelectric chemical characterizations demonstrated that Ag/Ag₂S/Ti₃C₂T _X heterojunctions provided effective channels for the reverse and synergistic migration of electrons and holes, leading to improved spatial separation. Notably, the Ag component in the composite acts as an electron acceptor and reactive center, significantly enhancing the migration ability of photogenerated electrons. The total alcohol yield over Ag/Ag₂S/Ti₃C₂T _X (125.3 μmol g_catal. ^-1) was 5.1 times higher than that on Ag₂S (24.7 μmol g_catal. ^-1) and 2.1 times higher than on Ti₃C₂T _X (60.7 μmol g_catal. ^-1). This study offers valuable insights into designing efficient photocatalytic CO₂ reduction catalysts.