Nanometric NaYF4 as an Unconventional Support for Gold Catalysts for Oxidation Reactions
Author(s) -
Shashank Mishra,
F. Morfin,
Violaine Mendez,
P.N. Swamy,
JeanMarc Rousset,
S. Danièle
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b00173
Subject(s) - catalysis , isostructural , x ray photoelectron spectroscopy , metal , materials science , nanoparticle , oxide , colloidal gold , inorganic chemistry , chemistry , chemical engineering , nanotechnology , crystallography , crystal structure , organic chemistry , engineering
The metal-support interaction plays an important role in gold catalysis. We employ here crystalline cubic (α-) and hexagonal (β-) phases of heterometallic fluoride NaYF 4 nanoparticles (NPs), obtained by the decomposition of a single source precursor [NaY(TFA) 4 (diglyme)] (TFA = trifluoroacetate), as nonoxide supports for gold catalysts. Using an isostructural gadolinium analogue, we also obtained doped α-NaYF 4 :Gd 3+ and β-NaYF 4 :Gd 3+ NPs. A successful deposition of ∼1% by weight gold NPs of average size 5-6.5 nm on these doped and undoped metal fluorides using HAuCl 4 ·3H 2 O afforded Au/NaYF 4 catalysts which were thoroughly characterized by using several physicochemical techniques such as X-ray diffraction, Brunauer-Emmett-Teller analysis, high-resolution transmission electron microscopy, energy-dispersive X-ray spectrometry, and X-ray photoelectron spectroscopy. A comparative study of the above catalysts for different oxidation reactions show that while for the aerobic oxidation of trans -stilbene in solution phase, they are either better (in terms of stilbene conversion) or at par (in terms of trans -stilbene oxide yield) in comparison to the reference catalyst Au/TiO 2 of the World Gold Council, their activity toward CO oxidation reactions in gas phase remains much less than that of gold catalysts supported on metal oxides.
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