EPR studies of [O−·O2] complexes on MgO surface and their stabilization centers

1991 ◽  
Vol 44 (1) ◽  
pp. 171-177 ◽  
Author(s):  
A. M. Volodin
2005 ◽  
Vol 44 (2) ◽  
pp. 861-864 ◽  
Author(s):  
Yeonjin Yi ◽  
Sangwan Cho ◽  
Myungkeun Noh ◽  
Chung-Nam Whang ◽  
Kwangho Jeong ◽  
...  

1992 ◽  
Vol 42 (5) ◽  
pp. 1115-1139 ◽  
Author(s):  
Gianfranco Pacchioni ◽  
Giuseppe Cogliandro ◽  
Paul S. Bagus

2020 ◽  
Vol 7 (4) ◽  
pp. 1092-1101 ◽  
Author(s):  
Honghong Wang ◽  
Cheng Zhong ◽  
Qingxin Ma ◽  
Jinzhu Ma ◽  
Hong He

The reaction mechanisms and synergistic effects of NO2/O2 on the heterogeneous oxidation of SO2 to sulfate on a MgO surface.


1999 ◽  
Vol 188 (1-2) ◽  
pp. 313-324 ◽  
Author(s):  
K. Asakura ◽  
H. Nagahiro ◽  
N. Ichikuni ◽  
Y. Iwasawa

2000 ◽  
Vol 07 (03) ◽  
pp. 277-306 ◽  
Author(s):  
GIANFRANCO PACCHIONI

The electronic structure and chemisorption properties of the surface of ionic crystals are reviewed, with emphasis on two topics: a critical overview of the experimental and theoretical studies of the adsorption of CO on single crystal and polycrystalline MgO, and a discussion on the most important defect centers at the MgO surface — low-coordinated sites, single oxygen and magnesium vacancies, divacancies, and impurity or substitutional atoms. The two subjects are to some extent interconnected. From the detailed theoretical and experimental study of the adsorption of a nonreactive molecule like CO and from the comparison of experiments done on single crystal or thin films and on powder samples, one can learn about the nature and concentration of the defects at the surface. A more precise characterization of defects requires, however, a careful spectroscopic investigation and a direct comparison with quantum-chemical calculations of both geometric structure and observable properties. The combined theoretical–experimental approach offers new opportunities for a better understanding of the complexity of oxide surfaces.


Sign in / Sign up

Export Citation Format

Share Document