Catalysis on platinum surfaces probed using synchrotron-based core-level spectroscopies

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Abstract/Contents

Abstract
Probing chemical reactions on solid surfaces in situ remains a major challenge in heterogeneous catalysis, because most methods of surface characterization require ultrahigh vacuum (UHV) conditions. In addition, the effects of morphology, particle size, and chemical composition are frequently difficult to disentangle due to sample heterogeneity. This work addresses these limitations by applying synchrotron-based core-level spectroscopies to well-defined systems based on single crystals. With a view to developing improved electrocatalysts for the oxygen reduction reaction (ORR) in fuel cells, the behavior of oxygenated species on the Pt(111) and Pt/Rh(111) surfaces was examined in situ under both electrochemical and ambient-pressure conditions using high-energy-resolution fluorescence-detection x-ray absorption spectroscopy (HERFD XAS) and ambient-pressure x-ray photoelectron spectroscopy (APXPS), respectively.

Description

Type of resource text
Form electronic; electronic resource; remote
Extent 1 online resource.
Publication date 2013
Issuance monographic
Language English

Creators/Contributors

Associated with Miller, Daniel James
Associated with Stanford University, Department of Chemistry.
Primary advisor Nilsson, Anders, 1956-
Thesis advisor Nilsson, Anders, 1956-
Thesis advisor Chidsey, Christopher E. D. (Christopher Elisha Dunn)
Thesis advisor Dai, Hongjie, 1966-
Advisor Chidsey, Christopher E. D. (Christopher Elisha Dunn)
Advisor Dai, Hongjie, 1966-

Subjects

Genre Theses

Bibliographic information

Statement of responsibility Daniel James Miller.
Note Submitted to the Department of Chemistry.
Thesis Thesis (Ph.D.)--Stanford University, 2013.
Location electronic resource

Access conditions

Copyright
© 2013 by Daniel James Miller
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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