Optimum Balance of Cu+ and Oxygen Vacancies of CuO x -CeO2 Composites for CO Oxidation Based on Thermal Treatment

2019 ◽  
Vol 2019 (13) ◽  
pp. 1714-1723 ◽  
Author(s):  
Baolin Liu ◽  
Yizhao Li ◽  
Yali Cao ◽  
Lei Wang ◽  
Shaojun Qing ◽  
...  
Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 312 ◽  
Author(s):  
Antonella Glisenti ◽  
Andrea Vittadini

The effects of modifying the composition of LaCoO3 on the catalytic activity are predicted by density functional calculations. Partially replacing La by Sr ions has benefical effects, causing a lowering of the formation energy of O vacancies. In contrast to that, doping at the Co site is less effective, as only 3d impurities heavier than Co are able to stabilize vacancies at high concentrations. The comparison of the energy profiles for CO oxidation of undoped and of Ni-, Cu-m and Zn-doped (La,Sr)CoO3(100) surface shows that Cu is most effective. However, the effects are less spectacular than in the SrTiO3 case, due to the different energetics for the formation of oxygen vacancies in the two hosts.


2020 ◽  
Vol 20 (5) ◽  
pp. 2791-2802
Author(s):  
Duangamol Ongmali ◽  
Sakollapath Pithakratanayothin ◽  
Sureerat Jampa ◽  
Apanee Luengnaruemitrchai ◽  
Thanyalak Chaisuwan ◽  
...  

In this work, a ceria (CeO2) support was modified with titania (TiO2) by nanocasting using MCM-48 as a hard template and then loading Cu (as the nitrate salt) at different levels (3–9% by weight) by deposition-precipitation followed by calcination. The addition of TiO2 in MSP CeO2 revealed that the MSP CeO2 was significantly improved the oxygen vacancies of the catalyst by increasing the Ce3+ content from 38 to 75% and stabilizing the Ce3+ species by bonding with the oxygen as Ce(4f)-O(2p)-Ti(3d). Moreover, the bonding of MSP CeO2 with TiO2 generated the oxygen defect vacancies (s–Ti3+), allowing Cu2+ to occupy and be reduced to Cu+ during calcination. The smaller CeO2 crystallite size (2.7 nm) of 9Cu/CeO2–TiO2 increased the mass-specific CO-Oxidation, showing the best catalytic activity due to its highest redox properties, as determined by H2-TPR and also showing resistant property to water and carbon dioxide. Indeed, water was adsorbed on the Ce3+ sites, generating OHads which reacted with CO to form –COOH, resulting in CO2.


RSC Advances ◽  
2014 ◽  
Vol 4 (22) ◽  
pp. 11322-11330 ◽  
Author(s):  
Putla Sudarsanam ◽  
Baithy Mallesham ◽  
D. Naga Durgasri ◽  
Benjaram M. Reddy

Fe-doped CeO2 nano-oxide exhibited superior CO oxidation activity compared to pristine CeO2 due to its facile reducible nature, enhanced lattice strain, and ample oxygen vacancies.


RSC Advances ◽  
2016 ◽  
Vol 6 (74) ◽  
pp. 70653-70659 ◽  
Author(s):  
Yanjie Zhang ◽  
Yanyan Zhao ◽  
Han Zhang ◽  
Liyuan Zhang ◽  
Huipeng Ma ◽  
...  

Metal (Au or Pt)-modified CeO2 materials with excellent redox ability for the oxidation of CO to CO2 were prepared by a redox precipitation method and a certain amount (4.2%) of oxygen vacancies was necessary to improve the CO oxidation on Pt-CeO2.


RSC Advances ◽  
2014 ◽  
Vol 4 (25) ◽  
pp. 13145-13152 ◽  
Author(s):  
F. Romero-Sarria ◽  
J. J. Plata ◽  
O. H. Laguna ◽  
A. M. Márquez ◽  
M. A. Centeno ◽  
...  

2014 ◽  
Vol 4 (11) ◽  
pp. 3826-3834 ◽  
Author(s):  
Feng Zhang ◽  
Tao Li ◽  
Li Pan ◽  
Aravind Asthagiri ◽  
Jason F. Weaver

Strong binding on oxygen vacancies and metallic domains promotes CO oxidation on partially-reduced PdO(101), while adsorption only on metallic sites promotes CO oxidation when 2D oxide coexists with Pd(111).


2020 ◽  
Vol 10 (13) ◽  
pp. 4271-4281 ◽  
Author(s):  
Ching-Shiun Chen ◽  
Tse-Ching Chen ◽  
Hung-Chi Wu ◽  
Jia-Huang Wu ◽  
Jyh-Fu Lee

Ce and Cu species deposited on TiO2 can apparently provide a higher turnover frequency rate and lower activation energy than the Cu/TiO2 catalyst and the Ce and Cu species on SiO2 catalysts.


2009 ◽  
Vol 5 ◽  
pp. 177-183 ◽  
Author(s):  
A. Susarrey-Arce ◽  
M. Herrera-Zaldívar ◽  
W. de la Cruz ◽  
Umapada Pal

Cathodoluminescence (CL) quenching was observed in ZnO nanostructures when doped with Yb by both chemical and physical methods. CL spectra of the samples revealed a defect emission at 2.25 eV in samples prepared by the chemical method, and an emission at 2.5 eV in samples prepared by the physical method. From the thermal treatment studies, it was found that oxygen vacancies are responsible for the 2.5 eV emission. Observed CL quenching in ZnO is explained through the participation of point defects in the energy transfer process from ZnO to Yb3+.


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