Ball-flower like CoS/g-C3N4 heterojunction photocatalyst for efficient and selective reduction of CO2 to CH4

The efficient and selective reduction of CO2 to hydrocarbon fuels via photocatalytic reaction is an ideal choice for alleviating environmental pollution and utilizing clean energy. Herein, the CoS/g-C3N4 heterojunction materials with different CoS mass ratios (10 wt%, 20 wt%, 30 wt%, and 40 wt%) were successfully prepared by ultrasonic -mechanical mixing, and applied for photoreduction of carbon dioxide for the first time. The formed p -n-type heterojunction can effectively slow down the recombination of photogenerated electron-hole pairs. The CoS/g-C3N4 composite exhibits excellent photocatalytic activity and stability for CO2 reduction under visible light. After 3-hour illumination, the maximum CH4 yield over the 20 wt% CoS/g-C3N4 sample reaches 121.74 mu mol/gcat, which was 21.06 times and 5.44 times that of g-C3N4 and CoS monomers. Furthermore, the CO production is negligible compared to CH4, indicating the superior product selectivity of the composite catalyst. Such significant promotion can be attributed to the well-matched energy band in the p -n heterojunction and the derived internal electric field, which results in a facilitated transfer of photogenerated charges as well as an improved utilization of visible light. This work well demonstrates that constructing heterojunctions is effective way to ameliorate the photocatalytic reduction of CO2.

Automated summary

In this study, CoS/g-C3N4 heterojunction materials with different CoS mass ratios were prepared and applied for the first time in the photocatalytic reduction of CO2. The p-n-type heterojunction effectively reduces the recombination of electron-hole pairs and enhances the utilization of visible light. The CoS/g-C3N4 composite exhibits excellent photocatalytic activity and selectivity for CH4 production, making it a promising catalyst for CO2 reduction.