Regulating Photocatalytic CO2 Reduction Kinetics through Modification of Surface Coordination Sphere

Solar-driven reduction of CO2 to value-added products represents a sustainable strategy for mitigating the greenhouse effect and addressing the related green-energy crisis. Herein, it is demonstrated that modifying the surface coordination sphere can significantly enhance the reaction kinetics and overall efficiency of CO2 reduction. More specifically, the decoration of isolated Mn atoms over the multi-edged TiO2 nano-pompons (Mn/TONP) upshifts the d-band center that allows favorable CO2 adsorption. Ultrafast spectroscopy demonstrates the greatly accelerated charge transfer between photoexcited multi-edged TONP and the newly implanted Mn reactive centers, supplying long-lifetime electrons to reduce absorbed CO2 molecules. By integrating adsorption and activation functions into the newly decorated Mn sites, the developed photocatalyst demonstrate impressive capacity for CO2 reduction (80.51 mmol g(-1) h(-1)). The surface modulation strategy at the atomic level not only opens new avenues for regulating the reaction kinetics toward photocatalytic CO2 reduction, but also paves the way for the rational design of highly efficient and selective photocatalysts for clean energy conversion.

Automated summary

This study demonstrates the enhancement of solar-driven CO2 reduction by modifying the surface coordination sphere. Decorating Mn atoms onto multi-edged TiO2 nano-pompons significantly improves CO2 adsorption and enables efficient charge transfer for reduction. The surface modulation strategy opens new avenues for photocatalytic CO2 reduction and rational design of highly efficient catalysts for clean energy conversion.