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Dynamic Behavior of Intermediate Adsorbates to Control Activity and Product Selectivity in Heterogeneous Catalysis : Methanol Decomposition on Pt/TiO2(110)

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Title: Dynamic Behavior of Intermediate Adsorbates to Control Activity and Product Selectivity in Heterogeneous Catalysis : Methanol Decomposition on Pt/TiO2(110)
Authors: Liu, Can Browse this author
Lu, Bang Browse this author
Ariga-Miwa, Hiroko Browse this author →KAKEN DB
Ogura, Shohei Browse this author
Ozawa, Takahiro Browse this author
Fukutani, Katsuyuki Browse this author
Gao, Min Browse this author
Hasegawa, Jun-ya Browse this author →KAKEN DB
Shimizu, Ken-ichi Browse this author →KAKEN DB
Asakura, Kiyotaka Browse this author →KAKEN DB
Takakusagi, Satoru Browse this author →KAKEN DB
Issue Date: 16-Aug-2023
Publisher: American Chemical Society
Journal Title: Journal of the American Chemical Society
Volume: 145
Issue: 36
Start Page: 19953
End Page: 19960
Publisher DOI: 10.1021/jacs.3c06405
Abstract: Dynamic behavior of intermediate adsorbates, such as diffusion, spillover, and reverse spillover, has a strong influence on the catalytic performance in oxide-supported metal catalysts. However, it is challenging to elucidate how the intermediate adsorbates move on the catalyst surface and find active sites to give the corresponding products. In this study, the effect of the dynamic behavior of methoxy intermediate on methanol decomposition on a Pt/TiO2(110) surface has been clarified by combination of scanning tunneling microscopy (STM), temperature-programmed desorption (TPD), and density functional theory (DFT) calculations. The methoxy intermediates were formed by the dissociative adsorption of methanol molecules on Pt nanoparticles at room temperature followed by spillover to the TiO2(110) support surface. TPD results showed that the methoxy intermediates were thermally decomposed at >350 K on the Pt sites to produce CO (dehydrogenation) and CH4 (C-O bond scission). A decrease of the Pt nanoparticle density lowered the activity for the decomposition reaction and increased the selectivity toward CH4, which indicates that the reaction is controlled by diffusion and reverse spillover of the methoxy intermediates. Time-lapse STM imaging and DFT calculations revealed that the methoxy intermediates migrate on the five-fold coordinated Ti (Ti-5c) sites along the [001] or [1 (1) over bar 0] direction with the aid of hydrogen adatoms bonded to the bridging oxygens (O-br) and can move over the entire surface to seek and find active Pt sites. This work offers an in-depth understanding of the important role of intermediate adsorbate migration in the control of the catalytic performance in oxide-supported metal catalysts.
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright c American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/articlesonrequest/AOR-BBBCDHY4WMSNPTATZ6GX
Type: article (author version)
URI: http://hdl.handle.net/2115/92977
Appears in Collections:触媒科学研究所 (Institute for Catalysis) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 高草木 達

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