The photocatalytic reduction of CO2 over Ag/TiO2 composites prepared with a simple silver mirror reaction method was investigated under UV-visible irradiation in both gas-phase (CO2 + water vapor) and aqueous solution (CO2-saturated NaHCO3 solution) systems. The as-prepared Ag/TiO2 nanocomposite exhibits efficient photocatalytic activity due to the surface plasmonic resonance and electron sink effect of the Ag component, which was found to be closely related to the size and loading amount of Ag. The rapid silver method is effective at curbing the size of Ag, so photocatalytic activity can be improved. Diverse organic chemical products were detected, including mainly methane and methanol as well as a small amount of C2 and C3 species such as acetaldehyde and acetone. Possible photocatalytic mechanisms were proposed. This artificial photosynthesis process may give a prosperous route to the removal of CO2 while simultaneously converting CO2 to valuable fuels based on highly efficient photocatalysts.
Mimicking natural photosynthesis in green plants, an all-solid-state Z-scheme was constructed for photocatalytic reduction of CO2 in the presence of water vapor, consisting of CdS nanospheres (CdS NSs) and TiO2nanoparticles as photocatalysts, and reduced graphene oxide (rGO) as a solid electron mediator. In this Z-scheme system, the photogenerated electrons from conductor band of TiO2 transfer to rGO, and then recombine with existing holes of CdS NSs, allowing that the photogenerated electrons enrich on the CdS semiconductor andholes on TiO2.The photocatalystic efficiency of the Z-scheme system exhibits remarkable enhancement relative to pure CdS, CdS/TiO2, and CdS/rGO.An all-solid-state Z-scheme was constructed for photocatalytic reduction of CO 2 , consisting of Cd Sand TiO 2 as photocatalysts, and reduced graphene oxide (rGO) as a solid electron mediator. The rapid electrontransfer between rGO and photocatalysts contributes to extension of the lifetime of photogenerated electrons,relative to higher photocatalytic CH 4 generation
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