Abstract
Precisely tailoring the distance between adjacent metal sites to match adsorption configurations of key species for the targeted reaction pathway is a great challenge in heterogeneous catalysis. Here, we report a proof-of-concept study on the atomically sites-tailored pathway in Pd-catalyzed acetylene hydrogenation, i.e., increasing the distance of adjacent Pd atoms (dPd-a-Pd ) for configuration matching in acetylene semi-hydrogenation against coupling. dPd-a-Pd is identified as a structural descriptor for describing the competitiveness for reaction pathways, and the increased dPd-a-Pd prefers the semi-hydrogenation pathway due to simultaneously promoted C2 H4 desorption and the destabilized transition state of the C2 H3 * coupling. Spectroscopic, kinetics and electronic structure studies reveal that increasing dPd-a-Pd to 3.31 Å delivers superior selectivity and stability due to energy matching and appropriate hybridization of Pd 4d with In 2s and, especially, 2p orbitals.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call