Exploring the visible light-assisted conversion of CO2 into methane and methanol, using direct Z-scheme TiO2@g-C3N4 nanosheets: synthesis and photocatalytic performance

The rapid growth of carbon dioxide (CO2) emissions raises concern about the possible consequences of atmospheric CO2 increase, such as global warming and greenhouse effect. Photocatalytic CO2 conversion has attracted researchers' interests to find a sustainable route for its elimination. In the present study, a direct Z-scheme TiO2/g-C3N4 composite (T-GCN) was fabricated via a facile hydrothermal route for the photocatalytic reduction of CO2 into methane (CH4) and methanol (CH3OH), under visible light irradiation without an electron mediator. The microstructure of the as-obtained TiO2/g-C3N4 nanocomposites was fully characterized for its physicochemical, structural, charge separation, electronic, and photo-excited carrier separation properties. The effect of CO2 and H2O partial pressure was studied to find the best operational conditions for obtaining maximum photocatalytic efficiency; the P-CO2 and P-H2O were 75.8 and 15.5 kPa, respectively, whereas, by increasing the light intensity from 20 to 80 mW/cm(2), a remarkable improvement in the reduction rate takes place (from 11.04 to 32.49 mu mol.gcat(-1).h(-1) methane production, respectively). Finally, under the most favorable light, P-CO2 and P-H2O conditions, high methanol and methane rates were obtained from the CO2 photocatalytic reduction through T-GCN (1.44 mu mol.gcat.(-1).h(-1) and 32.49 mu mol.gcat.(-1).h(-1), respectively) and an integrated proposition for the Z-scheme mechanism of photocatalytic reduction was proposed. This study offers a promising strategy to synthesize a Z-scheme T-GCN heterojunction with high photocatalytic performance for effective CO2 conversion.

Automated summary

The study focused on the photocatalytic reduction of CO2 into methane and methanol using a TiO2/g-C3N4 composite under visible light irradiation. The effect of CO2 and H2O partial pressure on photocatalytic efficiency was investigated, leading to the proposal of an integrated Z-scheme mechanism for effective CO2 conversion.