A Highly Stable Copper‐Based Catalyst for Clarifying the Catalytic Roles of Cu⁰ and Cu⁺ Species in Methanol Dehydrogenation

Abstract Identification of the active copper species, and further illustration of the catalytic mechanism of Cu‐based catalysts is still a challenge because of the mobility and evolution of Cu 0 and Cu + species in the reaction process. Thus, an unprecedentedly stable Cu‐based catalyst was prepared by uniformly embedding Cu nanoparticles in a mesoporous silica shell allowing clarification of the catalytic roles of Cu 0 and Cu + in the dehydrogenation of methanol to methyl formate by combining isotope‐labeling experiment, in situ spectroscopy, and DFT calculations. It is shown that Cu 0 sites promote the cleavage of the O−H bond in methanol and of the C−H bond in the reaction intermediates CH 3 O and H 2 COOCH 3 which is formed from CH 3 O and HCHO, whereas Cu + sites cause rapid decomposition of formaldehyde generated on the Cu 0 sites into CO and H 2 .

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