Nitrogen‐containing microporous carbon with specific morphology for non‐metallic catalytic NO oxidation at room temperature: The effect of morphology and nitrogen doping

Abstract

AbstractThe optimization of the gas diffusion path and surface coordination environment through morphology control can improve the intrinsic activity of the catalyst in NO oxidation reactions. Microporous nanosheets, nanowires, and spheres of carbon were constructed using resorcinol and formaldehyde as carbon sources, melamine as nitrogen source, and graphene oxide or carbon nanowires as structure‐directing agents to reveal the effects of morphology and nitrogen‐doping on NO oxidation activity at room temperature. With the increase of coating thickness, the ultramicroporous structure becomes pronounced and the nitrogen content increases, which contribute to the improvement of steady‐state NO conversion. The 2D microporous nanosheets (TDC‐200) with sheet structure shows prominent diffusion and adsorption capability than 1D nanowires and sphere, which shortens the gas diffusion path and enhances the efficient utilization of ultramicropores, thereby presenting the highest NO oxidation activity of 78.4% at room temperature. The results of DFT calculations further demonstrate that doping of nitrogen atoms could significantly reduce the (2NO + O2)ads energy barrier and accelerate the reaction. This study provides a deeper understanding of the NO oxidation on non‐metallic catalyst.