4.8 Article

Manipulating Copper Dispersion on Ceria for Enhanced Catalysis: A Nanocrystal-Based Atom-Trapping Strategy

期刊

ADVANCED SCIENCE
卷 9, 期 8, 页码 -

出版社

WILEY
DOI: 10.1002/advs.202104749

关键词

atom-trapping; colloidal nanocrystal; copper-ceria; water-gas shift reaction

资金

  1. U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science Program
  2. U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  3. Scientific User Facilities Division, Office of Basic Sciences, U. S. Department of Energy

向作者/读者索取更多资源

This study reports a nanocrystal-based atom-trapping strategy for accessing atomically precise Cu-CeO2 nanostructures to enhance catalytic performance. By utilizing the interfacial interactions between pre-synthesized Cu and CeO2 nanocrystals, Cu atoms can migrate and redisperse onto the surface of CeO2, allowing for the tuning of copper dispersion and the creation of CeO2 surface oxygen defects, resulting in improved catalytic activities and stabilities.
Due to tunable redox properties and cost-effectiveness, copper-ceria (Cu-CeO2) materials have been investigated for a wide scope of catalytic reactions. However, accurately identifying and rationally tuning the local structures in Cu-CeO2 have remained challenging, especially for nanomaterials with inherent structural complexities involving surfaces, interfaces, and defects. Here, a nanocrystal-based atom-trapping strategy to access atomically precise Cu-CeO2 nanostructures for enhanced catalysis is reported. Driven by the interfacial interactions between the presynthesized Cu and CeO2 nanocrystals, Cu atoms migrate and redisperse onto the CeO2 surface via a solid-solid route. This interfacial restructuring behavior facilitates tuning of the copper dispersion and the associated creation of surface oxygen defects on CeO2, which gives rise to enhanced activities and stabilities catalyzing water-gas shift reaction. Combining soft and solid-state chemistry of colloidal nanocrystals provide a well-defined platform to understand, elucidate, and harness metal-support interactions. The dynamic behavior of the supported metal species can be further exploited to realize exquisite control and rational design of multicomponent nanocatalysts.

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