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Ultrasound-mediated synthesis of nanoporous fluorite-structured high-entropy oxides toward noble metal stabilization

High-entropy oxides (HEOs) are an emerging class of advanced ceramic materials capable of stabilizing ultrasmall nanoparticle catalysts. However, their fabrication still relies on high-temperature thermal treatment methodologies affording nonporous architectures. Herein, we report a facile synthesis...

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Detalles Bibliográficos
Autores principales: Okejiri, Francis, Fan, Juntian, Huang, Zhennan, Siniard, Kevin Michael, Chi, Miaofang, Polo-Garzon, Felipe, Yang, Zhenzhen, Dai, Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048099/
https://www.ncbi.nlm.nih.gov/pubmed/35494219
http://dx.doi.org/10.1016/j.isci.2022.104214
Descripción
Sumario:High-entropy oxides (HEOs) are an emerging class of advanced ceramic materials capable of stabilizing ultrasmall nanoparticle catalysts. However, their fabrication still relies on high-temperature thermal treatment methodologies affording nonporous architectures. Herein, we report a facile synthesis of single-phase, fluorite-structured HEO nanocrystals via an ultrasound-mediated co-precipitation strategy under ambient conditions. Within 15 min of ultrasound exposure, high-quality fluorite-structured HEO (CeHfZrSnErO(x)) was generated as ultrasmall-sized particles with high surface area and high oxygen vacancy concentration. Taking advantage of these unique structural features, palladium was introduced and stabilized in the form of highly dispersed Pd nanoclusters within the CeHfZrSnErO(x) architecture. Neither phase segregation of the CeHfZrSnErO(x) support nor Pd sintering was observed under thermal treatment up to 900°C. The as-afforded Pd/CeHfZrSnErO(x) catalyst exhibits good catalytic performance toward CO oxidation, outperforming Pd/CeO(2) of the same Pd loading, which highlights the inherent advantage of CeHfZrSnErO(x) as carrier support over traditional oxides.