摘要
Water gas shift reaction (WGSR) is urgently calling for an alternative to the Fe-Cr catalyst. Ni-based catalysts are taken into consideration but remain challenging because of their high methanation activity. Here we report a highly active and selective NiC x /Ni-foam catalyst with clearly detectable Ni 3 C phase, facilely obtainable by endogenous growth of NiC 2 O 4 onto a Ni-foam and subsequent H 2 -reduction treatment. The preferred catalyst with high content of NiC x is capable of converting 63.6% or 94.3% CO at 350 °C or 400 °C with trace or < 0.8% CH 4 formation for a feed gas with H 2 O/CO/Ar molar ratio of 4/1/9, and is stable for at least 110 h. It is experimentally and theoretically unveiled that the Ni 3 C facilitates the dissociative activation of H 2 O and favors CO to form carboxylate species (favorable for CO 2 formation) rather than active Ni(CO) n intermediates for CH 4 formation thereby enabling the catalyst with high WGSR activity and selectivity.
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