Dynamic control and quantification of active sites on ceria for CO activation and hydrogenation

Ceria (CeO<sub>2</sub>) is a widely used oxide catalyst, yet the nature of its active sites remains elusive. This study combines model and powder catalyst studies to elucidate the structure-activity relationships in ceria-catalyzed CO activation and hydrogenation. Well-defined ceria clusters are synthesized on planar CeO<sub>2</sub>(111) and exhibit dynamic and tunable ranges of Ce coordination numbers, which enhance their interaction with CO. Reduced ceria clusters (e.g., Ce<sub>3</sub>O<sub>3</sub>) bind CO strongly and facilitate its dissociation, while near-stoichiometric clusters (e.g., Ce<sub>3</sub>O<sub>7</sub>) adsorb CO weakly and promote oxidation via carbonate formation. Unlike planar ceria surfaces, supported ceria clusters exhibit dynamic properties and enhanced catalytic activity, that mimic those of powder ceria catalysts. Insight from model studies provide a method to quantify active sites on powder ceria and guide further optimization of ceria catalysts for syngas conversion. This work marks a leap toward model-guided catalyst design and highlights the importance of site-specific catalysis.

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Publication Details

Journal
Nature Communications
Published
2024-11-07
DOI
https://doi.org/10.1038/s41467-024-53948-1
Citations
26
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
3.05

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article

Dynamic control and quantification of active sites on ceria for CO activation and hydrogenation

Yunjun Cao, Yangsheng Li, Qiang Fu, Wei-Peng Shao et al.
26 citations
Nature Communications
Catalytic Processes in Materials Science
3.05
article

Dynamic control and quantification of active sites on ceria for CO activation and hydrogenation

Yunjun Cao, Yangsheng Li, Qiang Fu, Wei-Peng Shao, Xinhe Bao, Zhiwen Zhou, Christof Wöll, Feng Jiao, Xiulian Pan, Na Li, Yi Zhang, Ping Liu, Zhi Liu, Fan Yang, Zeyu Zhou, Yunjian Ling
article en
26 citations

Abstract

Ceria (CeO<sub>2</sub>) is a widely used oxide catalyst, yet the nature of its active sites remains elusive. This study combines model and powder catalyst studies to elucidate the structure-activity relationships in ceria-catalyzed CO activation and hydrogenation. Well-defined ceria clusters are synthesized on planar CeO<sub>2</sub>(111) and exhibit dynamic and tunable ranges of Ce coordination numbers, which enhance their interaction with CO. Reduced ceria clusters (e.g., Ce<sub>3</sub>O<sub>3</sub>) bind CO strongly and facilitate its dissociation, while near-stoichiometric clusters (e.g., Ce<sub>3</sub>O<sub>7</sub>) adsorb CO weakly and promote oxidation via carbonate formation. Unlike planar ceria surfaces, supported ceria clusters exhibit dynamic properties and enhanced catalytic activity, that mimic those of powder ceria catalysts. Insight from model studies provide a method to quantify active sites on powder ceria and guide further optimization of ceria catalysts for syngas conversion. This work marks a leap toward model-guided catalyst design and highlights the importance of site-specific catalysis.

Nature CommunicationsVol. 15(1)
Karlsruhe Institute of Technology (DE), Dalian Institute of Chemical Physics (CN), Brookhaven National Laboratory (US), ShanghaiTech University (CN)
U.S. Department of Energy, Salt Science Research Foundation, National Natural Science Foundation of China, Office of Science, Basic Energy Sciences, Brookhaven National Laboratory
Openalex Percentile: Top 5%
Catalytic Processes in Materials Science
3.05
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