TY - JOUR
T1 - Design of a core–shell Pt–SiO2 catalyst in a reverse microemulsion system: Distinctive kinetics on CO oxidation at low temperature
AU - Al Mana, Noor
AU - Phivilay, Somphonh Peter
AU - Laveille, Paco
AU - Hedhili, Mohamed N.
AU - Fornasiero, Paolo
AU - Takanabe, Kazuhiro
AU - Basset, Jean-Marie
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: King Abdullah University of Science and Technology
PY - 2016/6/28
Y1 - 2016/6/28
N2 - The mechanism of formation of Pt@SiO2 as a model of core–shell nanoparticles via water-in-oil reverse microemulsions was studied in detail. By controlling the time of growth of Pt precursors, Pt(OH)x, after hydrolysis in NH3 aq. before adding SiO2 precursor (TEOS), Pt nanoparticles with a narrow size distribution were produced, from ultrafine metal nanoparticles (<1 nm) to 6 nm nanocrystals. Separately, the thickness of SiO2 was controllably synthesized from 1 to 15 nm to yield different Pt@SiO2 materials. The Pt@SiO2 core–shell catalysts exhibited a higher rate of CO oxidation by one order of magnitude with a positive order regarding CO pressure. The SiO2 shell did not perturb the Pt chemical nature, but it provided different coverage of CO in steady-state CO oxidation. © 2016 Elsevier Inc.
AB - The mechanism of formation of Pt@SiO2 as a model of core–shell nanoparticles via water-in-oil reverse microemulsions was studied in detail. By controlling the time of growth of Pt precursors, Pt(OH)x, after hydrolysis in NH3 aq. before adding SiO2 precursor (TEOS), Pt nanoparticles with a narrow size distribution were produced, from ultrafine metal nanoparticles (<1 nm) to 6 nm nanocrystals. Separately, the thickness of SiO2 was controllably synthesized from 1 to 15 nm to yield different Pt@SiO2 materials. The Pt@SiO2 core–shell catalysts exhibited a higher rate of CO oxidation by one order of magnitude with a positive order regarding CO pressure. The SiO2 shell did not perturb the Pt chemical nature, but it provided different coverage of CO in steady-state CO oxidation. © 2016 Elsevier Inc.
UR - http://hdl.handle.net/10754/621717
UR - https://linkinghub.elsevier.com/retrieve/pii/S0021951716300823
UR - http://www.scopus.com/inward/record.url?scp=84976428092&partnerID=8YFLogxK
U2 - 10.1016/j.jcat.2016.06.002
DO - 10.1016/j.jcat.2016.06.002
M3 - Article
SN - 0021-9517
VL - 340
SP - 368
EP - 375
JO - Journal of Catalysis
JF - Journal of Catalysis
ER -