4.7 Article

SOx on ceria from adsorbed SO2

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 134, Issue 18, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/1.3566998

Keywords

-

Funding

  1. Swedish Science Council (VR)
  2. National Natural Science Foundation of China [10674042, 10947001]
  3. Innovation Scientists and Technicians Troop Construction Projects of Henan Province, China [104200510014]

Ask authors/readers for more resources

Results from first-principles calculations present a rather clear picture of the interaction of SO2 with unreduced and partially reduced (111) and (110) surfaces of ceria. The Ce3+/Ce4+ redox couple, together with many oxidation states of S, give rise to a multitude of SOx species, with oxidation states from + III to + VI. SO2 adsorbs either as a molecule or attaches via its S-atom to one or two surface oxygens to form sulfite (SO32-) and sulfate (SO42-) species, forming new S-O bonds but never any S-Ce bonds. Molecular adsorption is found on the (111) surface. SO32- structures are found on both the (111) and (110) surfaces of both stoichiometric and partially reduced ceria. SO42-structures are observed on the (110) surface together with the formation of two reduced Ce3+ surface cations. SO2 can also partially heal the ceria oxygen vacancies by weakening a S-O bond, when significant electron transfer from the surface (Ce4f) into the lowest unoccupied molecular orbital of the SO2 adsorbate takes place and oxidizes the surface Ce3+ cations. Furthermore, we propose a mechanism that could lead to monodentate sulfate formation at the (111) surface. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3566998]

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available