Influence of surface oxygen vacancies on the catalytic activity of copper oxide

1992 ◽  
Vol 75 (3) ◽  
pp. 277-291 ◽  
Author(s):  
Andries Q.M. Boon ◽  
Fancine van Looij ◽  
John W. Geus
ChemCatChem ◽  
2018 ◽  
Vol 10 (18) ◽  
pp. 4100-4108 ◽  
Author(s):  
Huihui Ding ◽  
Jingxia Yang ◽  
Shuyi Ma ◽  
Nevzat Yigit ◽  
Jingli Xu ◽  
...  

2019 ◽  
Author(s):  
Noopur Jain ◽  
ahin roy ◽  
Angana De

This work compares the capacity of generating the surface oxygen vacancies over SrTiO<sub>3</sub>, BaTiO<sub>3</sub> and the mixed Sr<sub>0.5</sub>Ba<sub>0.5</sub>TiO<sub>3</sub>. This aspect is elucidated by significantly different chemical states of the elements on the surface of the three materials. Along with the fundamental materials aspect, CO oxidation studies complement the highest surface reducibility of the Sr<sub>0.5</sub>Ba<sub>0.5</sub>TiO<sub>3</sub> catalyst. With detailed adsorption-desorption studies, we report that the A-site cation substitution renders a better surface-reducibility induced catalytic activity for CO oxidation.


2019 ◽  
Author(s):  
Noopur Jain ◽  
ahin roy ◽  
Angana De

This work compares the capacity of generating the surface oxygen vacancies over SrTiO<sub>3</sub>, BaTiO<sub>3</sub> and the mixed Sr<sub>0.5</sub>Ba<sub>0.5</sub>TiO<sub>3</sub>. This aspect is elucidated by significantly different chemical states of the elements on the surface of the three materials. Along with the fundamental materials aspect, CO oxidation studies complement the highest surface reducibility of the Sr<sub>0.5</sub>Ba<sub>0.5</sub>TiO<sub>3</sub> catalyst. With detailed adsorption-desorption studies, we report that the A-site cation substitution renders a better surface-reducibility induced catalytic activity for CO oxidation.


2010 ◽  
Vol 16 (4) ◽  
pp. 1202-1211 ◽  
Author(s):  
Zhanfeng Zheng ◽  
Jaclyn Teo ◽  
Xi Chen ◽  
Hongwei Liu ◽  
Yong Yuan ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 772
Author(s):  
Yanxiong Liu ◽  
Changhua Hu ◽  
Longchun Bian

The correlation between the occurrence state of surface Pd species of Pd/CeO2 for lean CH4 combustion is investigated. Herein, by using a reduction-deposition method, we have synthesized a highly active 0.5% PdO/CeO2-RE catalyst, in which the Pd nanoparticles are evenly dispersed on the CeO2 nanorods CeO2-R. Based on comprehensive characterization, we have revealed that the uniformly dispersed Pd nanoparticles with a particle size distribution of 2.3 ± 0.6 nm are responsible for the generation of PdO and PdxCe1−xO2−δ phase with –Pd2+–O2−–Ce4+– linkage, which can easily provide oxygen vacancies and facilitate the transfer of reactive oxygen species between the CeO2-R and Pd species. As a consequence, the remarkable catalytic activity of 0.5% Pd/CeO2-RE is related to the high concentration of PdO species on the surface of the catalyst and the synergistic interaction between the Pd species and the CeO2 nanorod.


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