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Magnetic Fe(3)O(4)-Supported Gold Nanoflowers with Lattice-Selected Surfaces: Preparation and Catalytic Performance

[Image: see text] Nanoflowers (NFs)—shape-controlled noble metal nanocrystals—have garnered significant attention because of their novel catalytic properties and applicability. In this paper, we report the preparation and catalytic performance of a magnetic Fe(3)O(4)-supported AuNF catalyst with a c...

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Detalles Bibliográficos
Autores principales: Imura, Yoshiro, Kan, Ryota, Akiyama, Ryota, Saito, Haruna, Morita-Imura, Clara, Kawai, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331204/
https://www.ncbi.nlm.nih.gov/pubmed/32637851
http://dx.doi.org/10.1021/acsomega.0c02340
Descripción
Sumario:[Image: see text] Nanoflowers (NFs)—shape-controlled noble metal nanocrystals—have garnered significant attention because of their novel catalytic properties and applicability. In this paper, we report the preparation and catalytic performance of a magnetic Fe(3)O(4)-supported AuNF catalyst with a clean surface. The magnetically supported AuNFs were obtained by using magnetic Fe(3)O(4) as the support. However, when nonmagnetic γ-Al(2)O(3) was utilized as the support, the AuNFs did not exhibit a magnetic response. These supported AuNFs were utilized to catalyze the oxidation of 1-phenylethyl alcohol to acetophenone using air (1 atm) as the oxidant. The rate of formation of acetophenone using supported AuNFs was 8-fold higher than that of acetophenone using supported spherical Au nanoparticles of comparable size. In addition, the Fe(3)O(4)-supported AuNFs exhibited a higher rate of formation of acetophenone than the Al(2)O(3)-supported AuNFs. The Fe(3)O(4)-supported AuNFs were recovered using a magnet, and the recovered catalyst was reused under identical catalytic reaction conditions. The rate of formation of acetophenone using recovered Fe(3)O(4)-supported AuNFs remained unchanged, demonstrating no loss of catalytic activity.