Enhanced CH4 yields by interfacial heating-induced hot water steam during photocatalytic CO2 reduction

The adsorption and activation of H2O vapor on photocatalyst is highly important for CO2 reduction yet having been overlooked among the large amounts of reports. Herein, we demonstrate a preferential H2O adsorption mechanism to replace the previously assumed competitive adsorption, that is, H2O molecules were pre-adsorbed on the catalytic sites and dissociated to provide protons for the activation of the adsorbed CO2 molecules. Thanks to a photothermal membrane (PM)-induced interfacial heating, the generation of hot steam dramatically increases the partial pressure of water vapor from 17 to 43 kPa at ambient pressure, which favors H2O adsorption on TiO2 surface. The well-designed TiO2+PM system achieves selective reduction of CO2 to CH4 with a high evolution rate of 18.3 mu mol g(-1)h(-1), about 3.3 times of that in the absence of PM. The light-to-heat conversion makes the utilization of light energy more efficient, not merely for the photogeneration of charge carriers.

Automated summary

The study emphasizes the importance of H2O vapor adsorption and activation on photocatalysts for CO2 reduction, which has been overlooked in most reports. By utilizing a preferential adsorption mechanism and photothermal membrane-induced interfacial heating, efficient reduction of CO2 to CH4 with high evolution rates was achieved. The light-to-heat conversion process also enhances the utilization of light energy for more efficient performance.