Formation of hydrided Pt-Ce-H sites in efficient, selective oxidation catalysts

Single-atom site catalysts can improve the rates and selectivity of many catalytic reactions. We have modified Pt<sub>1</sub>/CeO<sub>2</sub> single sites by combining them with molecular groups and with oxygen vacancies of the support. The new sites include hydrided (Pt<sup>2+</sup>-Ce<sup>3+</sup>H<sup>δ-</sup>) and hydroxylated (Pt<sup>2+</sup>-Ce<sup>3+</sup>OH) sites that exhibit higher reactivity and selectivity to previous single sites for several reactions, including a ninefold increase in the reaction rate for carbon monoxide oxidation and a 2.3-fold improvement of propylene selectivity for oxidative dehydrogenation of propane. The atomic structure and reaction steps of these sites were determined with in situ and ex situ spectroscopy techniques and theoretical methods.

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Publication Details

Journal
Science
Published
2025-04-04
DOI
https://doi.org/10.1126/science.adv0735
Citations
39
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
20.19

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article

Formation of hydrided Pt-Ce-H sites in efficient, selective oxidation catalysts

Shengdong Tan, Siyang Yan, Shuchen Zhang, Sudong Chae et al.
39 citations
Science
Catalytic Processes in Materials Science
20.19
article

Formation of hydrided Pt-Ce-H sites in efficient, selective oxidation catalysts

Shengdong Tan, Siyang Yan, Shuchen Zhang, Sudong Chae, Yongqiang Q. Cheng, Lorenz J. Falling, Ji Su, Jiaxu Liu, Bingqing Yao, Yanbing Guo, Miquel Salmerón, Qian He, Zili Wu, Jeng‐Lung Chen, Xiao Zhao, Pragya Verma, Biluan Zhang, David Prendergast, Ji Yang, Slavomír Nemšák, Luke Daemen
article en
39 citations

Abstract

Single-atom site catalysts can improve the rates and selectivity of many catalytic reactions. We have modified Pt<sub>1</sub>/CeO<sub>2</sub> single sites by combining them with molecular groups and with oxygen vacancies of the support. The new sites include hydrided (Pt<sup>2+</sup>-Ce<sup>3+</sup>H<sup>δ-</sup>) and hydroxylated (Pt<sup>2+</sup>-Ce<sup>3+</sup>OH) sites that exhibit higher reactivity and selectivity to previous single sites for several reactions, including a ninefold increase in the reaction rate for carbon monoxide oxidation and a 2.3-fold improvement of propylene selectivity for oxidative dehydrogenation of propane. The atomic structure and reaction steps of these sites were determined with in situ and ex situ spectroscopy techniques and theoretical methods.

ScienceVol. 388(6746)
Oak Ridge National Laboratory (US), Lawrence Berkeley National Laboratory (US), National University of Singapore (SG), Dalian University of Technology (CN), Central China Normal University (CN), Dalian University (CN), National Synchrotron Radiation Research Center (TW), University of California, Berkeley (US)
U.S. Department of Energy, Alexander von Humboldt-Stiftung, National Research Foundation, National Research Foundation Singapore, National Science and Technology Council, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Oak Ridge National Laboratory, Lawrence Berkeley National Laboratory
Openalex Percentile: Top 0%
Catalytic Processes in Materials Science
20.19
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