Direct CO oxidation by lattice oxygen on the SnO2(110) surface: a DFT study

2014 ◽  
Vol 16 (24) ◽  
pp. 12488-12494 ◽  
Author(s):  
Zhansheng Lu ◽  
Dongwei Ma ◽  
Lin Yang ◽  
Xiaobing Wang ◽  
Guoliang Xu ◽  
...  
Keyword(s):  
Co Oxidation ◽  
Lattice Oxygen ◽  
Dft Study ◽  
Reduced Surface

The process of CO oxidation by lattice oxygen on the SnO2(110) surface and the recovery of the reduced surface by O2 is presented.

DFT study of CO oxidation on Cu2O–Au interfaces at Au–Cu alloy surfaces

RSC Advances ◽  
2015 ◽  
Vol 5 (2) ◽  
pp. 1587-1597 ◽  
Author(s):  
D. Liu ◽  
Y. F. Zhu ◽  
Q. Jiang
Keyword(s):  
Co Oxidation ◽  
Dft Study ◽  
Cu Alloy

CO oxidation on the Cu2O–Au interface at Au–Cu alloy surfaces.

Theoretical study of catalytic oxidation of CO on free PdxO2+ (x = 4–6) clusters: size dependent comparison of combustion

RSC Advances ◽  
2015 ◽  
Vol 5 (53) ◽  
pp. 42329-42340 ◽  
Author(s):  
Chandan Sahu ◽  
Deepanwita Ghosh ◽  
Abhijit K. Das
Keyword(s):  
Co Oxidation ◽  
Catalytic Oxidation ◽  
Theoretical Study ◽  
Dft Study ◽  
Oxidation Of Co ◽  
Catalytic Co Oxidation ◽  
Size Dependent ◽  
Catalytic Oxidation Of Co

A DFT study has been adopted to explore the catalytic CO oxidation on a free PdxO2+ (x = 4–6) cluster.

scholarly journals Tuning Pt-CeO2 interactions by high-temperature vapor-phase synthesis for improved reducibility of lattice oxygen

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Xavier Isidro Pereira-Hernández ◽  
Andrew DeLaRiva ◽  
Valery Muravev ◽  
Deepak Kunwar ◽  
Haifeng Xiong ◽  
...  
Keyword(s):  
High Temperature ◽  
Co Oxidation ◽  
Vapor Phase ◽  
Ambient Pressure ◽  
Lattice Oxygen ◽  
Single Atom ◽  
Stable Form ◽  
Phase Synthesis ◽  
Vapor Phase Synthesis ◽  
High Temperature Vapor

Abstract In this work, we compare the CO oxidation performance of Pt single atom catalysts (SACs) prepared via two methods: (1) conventional wet chemical synthesis (strong electrostatic adsorption–SEA) with calcination at 350 °C in air; and (2) high temperature vapor phase synthesis (atom trapping–AT) with calcination in air at 800 °C leading to ionic Pt being trapped on the CeO2 in a thermally stable form. As-synthesized, both SACs are inactive for low temperature (<150 °C) CO oxidation. After treatment in CO at 275 °C, both catalysts show enhanced reactivity. Despite similar Pt metal particle size, the AT catalyst is significantly more active, with onset of CO oxidation near room temperature. A combination of near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and CO temperature-programmed reduction (CO-TPR) shows that the high reactivity at low temperatures can be related to the improved reducibility of lattice oxygen on the CeO2 support.

A DFT Study of CO Oxidation at the Pd–CeO2(110) Interface

2015 ◽  
Vol 119 (49) ◽  
pp. 27505-27511 ◽  
Author(s):  
Weiyu Song ◽  
Yaqiong Su ◽  
Emiel J. M. Hensen
Keyword(s):  
Co Oxidation ◽  
Dft Study

How Temperature Affects the Mechanism of CO Oxidation on Au/TiO2: A Combined EPR and TAP Reactor Study of the Reactive Removal of TiO2 Surface Lattice Oxygen in Au/TiO2 by CO

ACS Catalysis ◽  
2016 ◽  
Vol 6 (8) ◽  
pp. 5005-5011 ◽  
Author(s):  
Daniel Widmann ◽  
Anke Krautsieder ◽  
Patrick Walter ◽  
Angelika Brückner ◽  
R. Jürgen Behm
Keyword(s):  
Co Oxidation ◽  
Lattice Oxygen ◽  
Tio2 Surface ◽  
Surface Lattice
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