Xin Hui, Li Rongtan, Lin Le, Mu Rentao, Li Mingrun, Li Dan, Fu Qiang, Bao Xinhe
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, iChEM, Chinese Academy of Sciences, Dalian, 116023, China.
Analytical & Testing Center, Sichuan University, Chengdu, Sichuan, 610064, China.
Nat Commun. 2024 Apr 10;15(1):3100. doi: 10.1038/s41467-024-47550-8.
In heterogeneous catalysis catalyst activation is often observed during the reaction process, which is mostly attributed to the induction by reactants. In this work we report that surface structure of molybdenum nitride (MoN) catalyst exhibits a high dependency on the partial pressure or concentration of reaction products i.e., CO and HO in reverse water gas-shift reaction (RWGS) (CO:H = 1:3) but not reactants of CO and H. Molybdenum oxide (MoO) overlayers formed by oxidation with HO are observed at reaction pressure below 10 mbar or with low partial pressure of CO/HO products, while CO-induced surface carbonization happens at reaction pressure above 100 mbar and with high partial pressure of CO/HO products. The reaction products induce restructuring of MoN surface into more active molybdenum carbide (MoC) to increase the reaction rate and make for higher partial pressure CO, which in turn promote further surface carbonization of MoN. We refer to this as the positive feedback between catalytic activity and catalyst activation in RWGS, which should be widely present in heterogeneous catalysis.
在多相催化中,催化剂活化常常在反应过程中被观察到,这主要归因于反应物的诱导作用。在本工作中,我们报道了氮化钼(MoN)催化剂的表面结构对反应产物(即逆水煤气变换反应(RWGS)(CO:H₂ = 1:3)中的CO和H₂O)的分压或浓度表现出高度依赖性,而对CO和H₂反应物则不然。在低于10毫巴的反应压力或CO/H₂O产物的低分压下,观察到由H₂O氧化形成的氧化钼(MoOₓ)覆盖层,而在高于100毫巴的反应压力和CO/H₂O产物的高分压下,会发生CO诱导的表面碳化。反应产物促使MoN表面重构为活性更高的碳化钼(MoC),以提高反应速率并导致更高的CO分压,这反过来又促进了MoN的进一步表面碳化。我们将此称为RWGS中催化活性与催化剂活化之间的正反馈,这种现象应该广泛存在于多相催化中。