Non-oxide supported Pt-metal-group catalysts for efficiently CO and toluene co-oxidation: Difference in water resistance and degradation intermediates

Herein, Pd and Pt-catalysts loaded on non-oxide support (g-C 3 N 4 ) were prepared and compared for CO and toluene co-oxidation, and Pt/C 3 N 4 presented excellent catalytic performance. A series of characterizations including TEM, H 2 -TPR, O 2 -TPR and XPS etc., indicated that Pt/C 3 N 4 exhibited the smaller Pt NPs, better low temperature reduction ability, more active oxygen species and positive charged Pt species, which could account for its better catalytic performance. Additionally, DFT calculations further confirmed that the lower activation barrier of O 2 and the higher adsorption for CO and toluene triggered the efficient CO and toluene degradation over Pt/C 3 N 4 . Interestingly, the introduction of H 2 O (10.0 vol%) suppressed the catalytic performance of Pd/C 3 N 4 , while expedited CO and toluene oxidation over Pt/C 3 N 4 , which was revealed by DFT calculations. Furthermore, the difference in degradation intermediates, corresponding distributions and toxicity generated during toluene oxidation under different conditions over Pd/C 3 N 4 and Pt/C 3 N 4 were exposed. Compared with Pd/C 3 N 4 , less variety, toxicity and content of intermediates produced over Pt/C 3 N 4 . This work would inspire many rational designs of supported noble metal catalysts for environmentally friendly catalysis.