Insights into the promotion role of phosphorus doping on carbon as a metal-free catalyst for low-temperature selective catalytic reduction of NO with NH 3 .

The catalytic reduction of NO with NH 3 (NH 3 -SCR) on phosphorus-doped carbon aerogels (P-CAs) was studied in the temperature range of 100-200 °C. The P-CAs were prepared by a one-pot sol-gel method by using phosphoric acid as a phosphorus source followed by carbonization at 600-900 °C. A correlation between catalytic activity and surface P content is observed. The P-CA-800 vac sample obtained via carbonization at 800 °C and vacuum treatment at 380 °C shows the highest NO conversion of 45.6-76.8% at 100-200 °C under a gas hourly space velocity of 500 h -1 for the inlet gas mixture of 500 ppm NO, 500 ppm NH 3 and 5.0 vol% O 2 . The coexistence of NH 3 and O 2 is essential for the high conversion of NO on the P-CA carbon catalysts, which can decrease the spillover of NO 2 and N 2 O. The main Brønsted acid sites derived from P-doping and contributed by the C-OH group at edges of carbon sheets are beneficial for NH 3 adsorption. In addition, the C 3 -P[double bond, length as m-dash]O configuration seems to have the most active sites for favorable adsorption and dissociation of O 2 and facilitates the formation of NO 2 . Therefore, the simultaneous presence of acidic groups for NH 3 adsorption and the C 3 -P[double bond, length as m-dash]O active sites for NO 2 generation due to the activation of O 2 molecules is likely responsible for the significant increase in the NH 3 -SCR activity over the P-CAs. The transformation of C 3 -P[double bond, length as m-dash]O to C-O-P functional groups after the reaction is found, which could be assigned to the oxidation of C 3 -P[double bond, length as m-dash]O by the dissociated O*, resulting in an apparent decrease of catalytic activity for P-CAs. The C-O-P based functional groups are also active in the NH 3 -SCR reaction.