Orientation-free and differentially pumped addition of a low-flux reactive gas beam to a surface analysis system.

Rev Sci Instrum

Department of Chemistry and Materials Science & Engineering Program, Washington State University, Pullman, Washington 99164, USA.

Published: November 2016

We describe an example of a piecewise gas chamber that can be customized to incorporate a low flux of gas-phase radicals with an existing surface analysis chamber for in situ and stepwise gas-surface interaction experiments without any constraint in orientation. The piecewise nature of this gas chamber provides complete angular freedom and easy alignment and does not require any modification of the existing surface analysis chamber. In addition, the entire gas-surface system is readily differentially pumped with the surface chamber kept under ultra-high-vacuum during the gas-surface measurements. This new design also allows not only straightforward reconstruction to accommodate the orientation of different surface chambers but also for the addition of other desired features, such as an additional pump to the current configuration. Stepwise interaction between atomic oxygen and a highly ordered pyrolytic graphite surface was chosen to test the effectiveness of this design, and the site-dependent O-atom chemisorption and clustering on the graphite surface were resolved by a scanning tunneling microscope in the nm-scale. X-ray photoelectron spectroscopy was used to further confirm the identity of the chemisorbed species on the graphite surface as oxygen.

Download full-text PDF

Source
http://dx.doi.org/10.1063/1.4966116DOI Listing

Publication Analysis

Top Keywords

surface analysis
12
graphite surface
12
differentially pumped
8
surface
8
gas chamber
8
existing surface
8
analysis chamber
8
chamber
5
orientation-free differentially
4
pumped addition
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!