Enhanced Photocatalytic CO2Reduction over TiO2Using Metalloporphyrin as the Cocatalyst

The photocatalytic reduction of carbon dioxide (CO2) into CO and hydrocarbon fuels has been considered as an ideal green technology for solar-to-chemical energy conversion. The separation/transport of photoinduced charge carriers and adsorption/activation of CO(2)molecules play crucial roles in photocatalytic activity. Herein, tetrakis (4-carboxyphenyl) porphyrin (H2TCPP) was incorporated with different metal atoms in the center of a conjugate macrocycle, forming the metalloporphyrins TCPP-M (M = Co, Ni, Cu). The as-obtained metalloporphyrin was loaded as a cocatalyst on commercial titania (P25) to form TCPP-M@P25 (M = Co, Ni, Cu) for enhanced CO(2)photoreduction. Among all of the TCPP-M@P25 (M = Co, Ni, Cu), TCPP-Cu@P25 exhibited the highest evolution rates of CO (13.6 mu mol.g(-1).h(-1)) and CH4(1.0 mu mol.g(-1).h(-1)), which were 35.8 times and 97.0 times those of bare P25, respectively. The enhanced photocatalytic activity could be attributed to the improved photogenerated electron-hole separation efficiency, as well as the increased adsorption/activation sites provided by the metal centers in TCPP-M (M = Co, Ni, Cu). Our study indicates that metalloporphyrin could be used as a high-efficiency cocatalyst to enhance CO(2)photoreduction activity.