The synergy of in situ-generated Ni0 and Ni2P to enhance CO adsorption and protonation for selective CH4 production from photocatalytic CO2 reduction.

The selective photocatalytic reduction of CO2 to CH4 remains a challenge because there is a need for not only strong adsorption sites for the intermediates, but also optimal proton-feeding sites on the photocatalyst surface. Herein, a synergistic dual-site function between in situ-generated Ni0 and Ni2P on carbon nitride nanosheets (CN) for photocatalytic reduction of CO2 to CH4 is presented. The highest CH4 production rate of 69.03 μmol g−1 h−1 is achieved on Ni2P/CN-0.5 in an aqueous suspension. Detailed analyses show that the promotion of CH4 is closely correlated with the formation of Ni0 sites due to light irradiation, which is confirmed by tracking the compositions of Ni2P/CN-0.5 through XPS and HRTEM characterization. Density functional theory calculations have been combined with CO-TPD and in situ FTIR spectra to reveal the synergy between in situ-generated Ni0 sites and Ni2P. It shows that the Ni0 sites can stabilize the key intermediate *CO, while the Ni0–Ni2P interface can promote *H transfer from Ni2P to Ni0. Therefore, the CO intermediates are rapidly protonated to form CHO* instead of being desorbed from the surface to produce CO, and subsequently CHO* will be converted into CH4. This work demonstrates a new strategy of designing highly efficient photocatalysts with synergistic catalytic sites for CO2 conversion to hydrocarbons. [ABSTRACT FROM AUTHOR]