Highly efficient and 100 % selectivity of CO generation via CO2 Photoreduction over a novel CsBr@CuBr2 Heterojunction

Abstract

To address the global challenge posed by excessive carbon dioxide emissions, our research pioneers the transformation of CO2 into valuable hydrocarbon fuels. Central to this approach is the innovation of photocatalysts, engineered to exhibit exceptional photoresponse characteristics. In this research, the CsBr@CuBr2 photocatalyst was innovatively synthesized through a straightforward and effective one-pot method. The catalyst displayed remarkable efficacy, achieving a CO2 photoreduction rate of 201.47 μmol g−1 within just 4 h. The incorporation of CsBr into CuBr2 effectively captures excited-state electrons, thereby significantly enhancing charge separation efficiency. Utilizing in situ DRIFTS and DFT theoretical analysis, the experiment reveals the complex process of CO2 photoreduction to CO. The results of this experiment provide breakthrough insights for the systematic design of metal bromide heterostructures, which possess robust CO2 adsorption/activation potential and notable stability.

Keywords

• CO2
• Photocatalysis
• Reducing reaction
• CO
• CuBr2