Methane Activation and Coupling Pathways on Ni2P Catalyst

Abstract

The direct catalytic conversion of methane (CH4) to higher hydrocarbons has attracted considerable attention in recent years because of the increasing supply of natural gas. Efficient and selective catalytic conversion of methane to value-added products, however, remains a major challenge. Recent studies have shown that the incorporation of phosphorus atoms in transition metals improves their selectivity and resistance to coke formation for many catalytic reactions. In this work, we report a density function theory-based investigation of methane activation and C2 product formation on Ni2P(001). Our results indicate that, despite the lower reactivity of Ni2P relative to Ni, the addition of phosphorus atoms hinders excessive dehydrogenation of methane to CH* and C* species, thus reducing carbon deposition on the surface. CH3* and CH2* moieties, instead, are more likely to be the most abundant surface intermediates once the initial C–H bond in methane is activated with a barrier of 246 kJ mol−1. The formation of ethylene from 2CH2* on Ni2P is facile with a barrier of 56 kJ mol−1, which is consistent with prior experimental studies. Collectively, these findings suggest that Ni2P may be an attractive catalyst for selective methane conversion to ethylene.