Cargando…
The Preparation and Catalytic Properties of Nanoporous Pt/CeO(2) Composites with Nanorod Framework Structures
Pt/CeO(2) catalysts with nanoporous structures were prepared by the facile dealloying of melt-spun Al(92−X)Ce(8)Pt(X) (X = 0.1; 0.3 and 0.5) ribbons followed by calcination. The phase compositions and structural parameters of the catalysts were characterized by X-ray diffraction (XRD), field emissio...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566510/ https://www.ncbi.nlm.nih.gov/pubmed/31052543 http://dx.doi.org/10.3390/nano9050683 |
Sumario: | Pt/CeO(2) catalysts with nanoporous structures were prepared by the facile dealloying of melt-spun Al(92−X)Ce(8)Pt(X) (X = 0.1; 0.3 and 0.5) ribbons followed by calcination. The phase compositions and structural parameters of the catalysts were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HRTEM). The specific surface area and pore size distribution were characterized by N(2) adsorption–desorption tests. The catalytic properties were evaluated by a three-way catalyst (TWC) measurement system. The results revealed that the dealloyed samples exhibited a nanorod framework structure. The Pt nanoparticles that formed in situ were supported and highly dispersed on the CeO(2) nanorod surface and had sizes in the range of 2–5 nm. For the catalyst prepared from the melt-spun Al(91.7)Ce(8)Pt(0.3) ribbons, the 50% CO conversion temperature (T(50)) was 91 °C, and total CO could be converted when the temperature was increased to 113 °C. An X-ray photoelectron spectroscopy (XPS) test showed that the Pt(0.3)/CeO(2) sample had a slightly richer oxygen vacancy; and a H(2) temperature-programmed reduction (H(2)-TPR) test demonstrated its superior adsorption ability for reduction gas and high content of active oxygen species. The experiments indicated that the catalytic performance could be retained without any attenuation after 130 h when water and CO(2) were present in the reaction gas. The favorable catalytic activities were attributed to the high specific areas and small pore and Pt particle sizes as well as the strong interactions between the CeO(2) and Pt nanoparticles. The Pt nanoparticles were embedded in the surface of the CeO(2) nanorods, inhibiting growth. Therefore, the catalytic stability and water resistance were excellent. |
---|