Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5423611 | Surface Science | 2009 | 7 Pages |
Abstract
Room temperature (RT) adsorption of nitric oxide (NO) on Ir(1Â 1Â 1) was studied by scanning tunneling microscopy (STM). At low exposures, NO molecules can not be imaged by STM, because at RT the diffusion of NO is much faster than the STM scanning speed. At high exposures near the saturation coverage, however, a well-ordered 2Â ÃÂ 2 structure is observed. The coverage of the major 2Â ÃÂ 2 species is 0.25 and they can be assigned to the NO molecules adsorbed on the Ir ontop sites. A small number of less bright spots are assigned to nitrogen atoms produced by dissociation. Their number increases by annealing the NO-saturated surface at 380Â K. A small number of another dissociation product, oxygen, are observed as black lines, indicating that the diffusion of oxygen atoms is fast. Scratch-like noise features were also detected by the STM, which suggests that a mobile precursor state exists, which was clearly shown by the effects of electron irradiation from the STM tip. These results are consistent with the previous molecular beam studies. Hopping of the 2Â ÃÂ 2 ordered NO species was frequently observed at the anti-phase domain boundaries and edges of the 2Â ÃÂ 2 islands.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Masuaki Matsumoto, Shohei Ogura, Katsuyuki Fukutani, Tatsuo Okano,