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Inverse iron oxide/metal catalysts from galvanic replacement

Key chemical transformations require metal and redox sites in proximity at interfaces; however, in traditional oxide-supported materials, this requirement is met only at the perimeters of metal nanoparticles. We report that galvanic replacement can produce inverse FeO(x)/metal nanostructures in whic...

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Detalles Bibliográficos
Autores principales: Zhu, Yifeng, Zhang, Xin, Koh, Katherine, Kovarik, Libor, Fulton, John L., Rosso, Kevin M., Gutiérrez, Oliver Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324589/
https://www.ncbi.nlm.nih.gov/pubmed/32601487
http://dx.doi.org/10.1038/s41467-020-16830-4
Descripción
Sumario:Key chemical transformations require metal and redox sites in proximity at interfaces; however, in traditional oxide-supported materials, this requirement is met only at the perimeters of metal nanoparticles. We report that galvanic replacement can produce inverse FeO(x)/metal nanostructures in which the concentration of oxide species adjoining metal domains is maximal. The synthesis involves reductive deposition of rhodium or platinum and oxidation of Fe(2+) from magnetite (Fe(3)O(4)). We discovered a parallel dissolution and adsorption of Fe(2+) onto the metal, yielding inverse FeO(x)-coated metal nanoparticles. This nanostructure exhibits the intrinsic activity in selective CO(2) reduction that simple metal nanoparticles have only at interfaces with the support. By enabling a simple way to control the surface functionality of metal particles, our approach is not only scalable but also enables a versatile palette for catalyst design.