CO Oxidation Mechanism on CeO2-Supported Au Nanoparticles
نویسندگان
چکیده
منابع مشابه
CO oxidation mechanism on CeO(2)-supported Au nanoparticles.
Density functional theory was used to study the CO oxidation catalytic activity of CeO(2)-supported Au nanoparticles (NPs). Experimental observations on CeO(2) show that the surface of CeO(2) is enriched with oxygen vacancies. We compare CO oxidation by a Au(13) NP supported on stoichiometric CeO(2) (Au(13)@CeO(2)-STO) and partially reduced CeO(2) with three vacancies (Au(13)@CeO(2)-3VAC). The ...
متن کاملCO Oxidation at the Interface between Doped CeO2 and Supported Au Nanoclusters.
DFT+U calculations of CO oxidation by Au13 nanoclusters (NCs) supported on either CeO2 or doped (X-Ce)O2 (X = Au, Pt, Pd, Ti, Ru, Zr) show that doping the CeO2 support accelerates CO oxidation by the Mars-van Krevelen mechanism at the Au-(X-Ce)O2 interface. We find that Au, Pd, Pt, and Ti dopants significantly lower the vacancy formation energy of the CeO2 support and that electron donation fro...
متن کاملAu/CeO2 Catalysts: Structure and CO Oxidation Activity
In this comprehensive review, the main aspects of using Au/CeO2 catalysts in oxidation reactions are considered. The influence of the preparation methods and synthetic parameters, as well as the characteristics of the ceria support (presence of doping cations, oxygen vacancies concentration, surface area, redox properties, etc.) in the dispersion and chemical state of gold are revised. The prop...
متن کاملCO oxidation on h-BN supported Au atom.
The mechanism of CO oxidation by O(2) on Au atoms supported on the pristine and defected hexagonal boron nitride (h-BN) surface has been studied theoretically using density functional theory. It is found that O(2) binds stronger than CO on an Au atom supported on the defect free h-BN surface and h-BN surface with nitrogen vacancy (V(N)@h-BN), but weaker than CO on a free Au atom or Au trapped b...
متن کاملGold nanoparticles supported on magnesium oxide for CO oxidation
Au was loaded (1 wt%) on a commercial MgO support by three different methods: double impregnation, liquid-phase reductive deposition and ultrasonication. Samples were characterised by adsorption of N2 at -96°C, temperature-programmed reduction, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy and X-ray diffraction. Upon loading with Au, MgO changed into Mg(...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of the American Chemical Society
سال: 2012
ISSN: 0002-7863,1520-5126
DOI: 10.1021/ja207510v