Atomically dispersed Ru(III) on N-doped mesoporous carbon hollow spheres as catalysts for CO2 hydrogenation to formate

Abstract

Atomically dispersed Ru(III) catalysts on hierarchical and porous supports show great potential for application in the catalysis of the hydrogenation of CO2 to formate due to their high catalytic activity and stability. In this study, heterogeneous Ru(III) catalysts on N-doped mesoporous carbon hollow spheres (N-MCHS) were synthesized through a SiO2-templated resorcinol-formaldehyde polymer pyrolysis at different temperatures. At low pyrolysis temperatures (700-800 degrees C), the dominant N species on the catalysts were found to be pyrrolic and pyridinic N (N-pyrrolic and N-pyridinic). However, the dominant N species on the samples produced from 900 to 1000 degrees C was graphitic N (N-graphitic). The highest catalytic activities on the batch hydrogenation experiments were recorded on the catalysts with the predominant Ru-N-graphitic active sites. Using the Ru/N-MCHS-900 catalyst, the turn-over number (TON) was as high as 7550 after the hydrogenation for 2 h at 120 degrees C and 8 MPa. On the other hand, the Ru/N-MCHS-700 catalyst exhibited excellent stability in both batch and continuous reactors. No noticeable deactivation was observed even after 72 h of continuous hydrogenation, which can be attributed to the strong binding energy between the Ru(III) species, and the N-pyridinic and N-pyrrolic sites on the N-MCHS supports. This study provided significant insights for the development of novel heterogeneous catalyst systems for the hydrogenation of CO2 to formate.