journal article·2017-07

Confining the Nucleation of Pt to In Situ Form (Pt‐Enriched Cage)@CeO2 Core@Shell Nanostructure as Excellent Catalysts for Hydrogenation Reactions

Shuyan Song, Xianchun Liu, Junqi Li, Jing Pan, Fan Wang, Yan Xing, Xiao Wang, Xiaogang Liu, Hongjie Zhang

Advanced Materials· Volume 29· Issue 28
Publisher page

Abstract

Ultrathin (Pt‐enriched cage)@CeO2 core@shell nanostructures are successfully fabricated via a facile hard‐template method. It is found that the usage of Pd@Ag@CeO2 bi‐metallic core@shell nanostructure as the hard template plays an important role in avoiding the independent nucleation of Pt metal during the galvanic replacement process between K2PtCl4 and Ag components. This unique core@shell samples show extraordinary activity and selectivity for the cinnamaldehyde hydrogenation reaction. It can achieve over 95% conversion with 87% selectivity of hydrocinnamaldehyde in 5 h under 1 atm H2 pressure. It is considered that such high catalytic performance could be attributed to the densely CeO2‐coated core@shell hybrid form as well as the ultrathin nature of the Pt‐enriched cage.
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Research context

OpenAlex topics: Nanomaterials for catalytic reactions · Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 P. R. China

College of Chemistry Northeast Normal University Changchun 130024 P. R. China

Changchun Institute of Applied Chemistry University of Chinese Academy of Sciences Beijing 100049 P. R. China

Department of Chemistry National University of Singapore 117543 Singapore

Funding

National Natural Science Foundation of China · Commonwealth Scientific and Industrial Research Organisation · Youth Innovation Promotion Association of the Chinese Academy of Sciences · Chinese Academy of Sciences

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