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• W3204361830 startingPage "26342" @default.
• W3204361830 abstract "Abstract For the activity of a nano‐catalyst, a general and quantitative solution to building direct structure–reactivity relationship has not yet been established. On top of the first‐principle‐based kinetic Monte Carlo (KMC) simulations, we developed a model to build the adsorption site dependence of the activity. We applied this model to study the nano effects of Cu catalysts in the water‐gas shift reaction. By accumulating the activities of different adsorption sites, our model satisfactorily reproduced the experimental apparent activation energies for catalysts with sizes over hundreds of nanometers, which were out of reach for conventional KMC simulations. Our results disclose that, even for a cubic catalyst with size of 877 nm, its activity can still be closely related to the activity of edge sites, instead of only the exposed Cu(100) facets as might be expected. The present model is expected to be useful for systems that are controlled by the hydrogenation/dehydrogenation processes." @default.
• W3204361830 created "2021-10-11" @default.
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• W3204361830 date "2021-11-10" @default.
• W3204361830 modified "2023-09-24" @default.
• W3204361830 title "Structure–Reactivity Relationship for Nano‐Catalysts in the Hydrogenation/Dehydrogenation Controlled Reaction Systems" @default.
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• W3204361830 doi "https://doi.org/10.1002/anie.202109942" @default.
• W3204361830 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34626058" @default.
• W3204361830 hasPublicationYear "2021" @default.
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