摘要：To improve the photocatalytic oxidation reaction activity for NO removal, photocatalysts with excellent activity are required to activate molecular oxygen. Solid solution and heterojunction were suggested as effective strategies to enhance the molecular oxygen activation viaexciton and carrier photocatalysis. In this study, a solid solution and heterojunction containing BiOBr0.5I0.5/BiOI catalyst was synthesized, and it showed improved photocatalytic activity for removing NO. The photocatalytic NO removal mechanism indicated that synergistic effects between the solid solution and heterojunction induced the enhanced activity for molecular oxygen activation. The photogenerated holes, superoxide, and singlet oxygen generated by the carrier and exciton photocatalysis supported the high photocatalytic NO removal efficiency. This study provides new ideas for designing efficient Bi-O-X(X = Cl, Br, I) photocatalysts for oxidation reactions.

摘要：Solar‐energy‐driven catalytic CO_(2) reduction for the production of value‐added carbon‐based materials and chemical raw materials has attracted great interest to alleviate the global climate change and energy *** production of multicarbon(C2)products through CO_(2) reduction is extremely attractive,however,the yield and selectivity of C2 products remain low because of the low reaction temperature required and the low photoelectron density of the ***,we introduce WO3–x,which contains oxygen vacancies and exhibits an excellent photothermal conversion efficiency,to improve the generation of C2 products(C2H4 and C2H6)under simulated sunlight(UV‐Vis‐IR)***3–x produced 5.30 and 0.93μmol·g^(–1)C2H4 and C2H6,respectively,after 4 h,with a selectivity exceeding 34%.In situ Fourier transform infrared spectra and theoretical calculations showed that the oxygen vacancies enhanced the water activation and hydrogenation of adsorbed CO for the formation of C2 products via C–C coupling from CH2/CH3 *** findings of this study could assist in the design of highly active solar‐energy‐driven catalysts to produce C–C coupling products through CO2 reduction.