A metal-free electrochemically exfoliated graphene/graphitic carbon nitride nanocomposite for CO2 photoreduction to methane under visible light irradiation

In this work, an electrochemically exfoliated graphene/graphite carbon nitride ((EG)/g-C3N4) heterojunction photocatalyst was synthesized for CO2 photoreduction to methane. Different photocatalyst samples with various EG loadings were prepared by the impregnation-calcination method, and their photoreduction performances were tested in a continuous-flow CO2 photoreactor under visible light irradiation. Results indicated that the best -performing photocatalyst (0.075 EG-CN) revealed the highest CH4 evolution of 21.32 mu mol gcatalyst -1 after 6 h of light irradiation that manifested a significant 7.25-fold enhancement in CH4 production compared to the pure CN with 98.6% selectivity for CH4 production. The developed photocatalyst was extensively analyzed using SEM, TEM, XRD, FTIR, BET and XPS characterizations, and the relationship between the physicochemical properties of the photocatalyst and its CO2 photoreduction performance was extensively discussed. The PL, TPR, and UV-Vis tests showed that introducing the EG into the photocatalyst enhanced the visible light absorptions and facilitated the fast transfer and separation of photogenerated electron-hole. The mechanism of visible-light photoreduction of CO2 to CH4 with EG-CN nanocomposite was also proposed and discussed. The optimum photocatalyst possessed high stability after four consecutive cycles of CO2 photoreduction to CH4 at ambient conditions without any significant change in the CH4 production.

Automated summary

In this study, an electrochemically exfoliated graphene/graphite carbon nitride ((EG)/g-C3N4) heterojunction photocatalyst was synthesized for CO2 photoreduction to methane. The best-performing photocatalyst (0.075 EG-CN) showed a significant enhancement in CH4 production with 98.6% selectivity after 6 hours of light irradiation compared to pure CN. The developed photocatalyst exhibited high stability after consecutive cycles of CO2 photoreduction to CH4.