Self-nitrogen-doped hierarchical porous carbon spheres as metal-free catalyst for efficient photocatalytic CO2 reduction

It is rather important to develop an efficient, stable and economical photocatalyst for solar-driven CO2 reduction. Herein, N-doped hierarchical porous carbon spheres (NPCS-F6) with metal-like activity is synthesized using acrylamide and F127 as nitrogen source and soft template, and the effective synergy between nitrogen-containing species and hierarchical pore structure makes the samples exhibit excellent CO2 reduction properties. XPS characterization illustrated that the introduced pyridine nitrogen and pyrrole nitrogen groups contribute to the increase of CO2 reduction sites on the surface of the material. N2 adsorption analyses verified the existence of hierarchical pore structures in which micropores facilitate the exposure of more adsorption active sites, while mesopores and macropores can be used as transfer channels to connect the internal micropores and reduce the molecular diffusion resistance to improve CO2 adsorption performance. In addition, the pore structure of the samples prepared with P123 and CTAB as templates was mainly microporous, whereas carbon spheres with hierarchical pores coexisting were obtained with F127 as template. The evaluation of photocatalytic CO2 reduction activity showed that the CO yield of NPCS-F6 could reach 17.56 μmol·g−1 for 8 h, which was 1.17 times, 1.08 times and 1.07 times of the original NCS-8 (15.05 μmol·g−1), NPCS-P6 (P123 as soft template, 16.25 μmol·g−1) and NPCS-C1 (CATB as soft template, 16.39 μmol·g−1), respectively. Comprehensive characterization results were analyzed to propose a possible mechanism for photocatalytic CO2 reduction, in which photogenerated electron-hole pairs are generated inside the material under light conditions, and the photogenerated electrons are transferred to the N-6/N-5 active sites through the electron transfer channel N-Q to react with CO2 molecules adsorbed on the surface to be reduced to CO. Finally, our results provide a favorable and feasible strategy to synthesize metal-free photocatalysts for high-efficiency CO2 adsorption and targeted reduction of CO2 to CO.