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Ultra-fine platinum species supported on niobium pentoxide for CO oxidation
Platinum oxide supported on a Lewis acid niobium oxide (Nb(2)O(5)) support has been used for various heterogeneous and homogeneous catalysts. In this work, we used urea as a precipitating agent to obtain crystallized Nb(2)O(5) with high surface area via a hydrothermal route. Nb(2)O(5)-supported Pt c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050684/ https://www.ncbi.nlm.nih.gov/pubmed/35497582 http://dx.doi.org/10.1039/d0ra01252a |
Sumario: | Platinum oxide supported on a Lewis acid niobium oxide (Nb(2)O(5)) support has been used for various heterogeneous and homogeneous catalysts. In this work, we used urea as a precipitating agent to obtain crystallized Nb(2)O(5) with high surface area via a hydrothermal route. Nb(2)O(5)-supported Pt catalysts were subsequently synthesized via an incipient wetness impregnation approach. Multiple characterizations including X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and nitrogen adsorption/desorption confirmed the identical structural and textural properties of the Nb(2)O(5) support before and after the impregnation process. Furthermore, the X-ray absorption fine structure technique (XAFS) results with related data analysis indicate that the platinum species in the fresh and H(2)-pretreated samples were in the form of single atoms or ultrafine clusters. In addition, the decrease in coordination number (CN) of the first-shell Pt–O bond, as well as the formation of Pt–Pt contribution with very low CN, after H(2)-pretreatment was verified, which corresponds to the decrease of oxidation state for Pt species on the surface of supports. Thus, the ultrafine-clustered metallic Pt species are considered to be more active than the oxidized Pt single ions. The current results will be of great significance in controllable synthesis of active Pt-based catalysts for other catalytic oxidation reactions. |
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