The adsorption of CO on Pt ( I 11) and Pt ( 100) single crystal surfaces in an aqueous acid solution was studied by IRRAS and CV. On-top and bridge-bonded CO species adsorbed on Pt( I 11) and Pt( 100) electrodes were detected.
Hydrogen adsorption on Pt(100), Pt(110), Pt(111) and Pt(1111) electrode surfaces studied by in situ infrared reflection absorption spectroscopy
โ Scribed by Hirohito Ogasawara; Masatoki Ito
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 503 KB
- Volume
- 221
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
HydrogenadsorptiononPt(lOO),Pt(ll 1 l)(6(l00)~(1ll)),Pt(llO)andPt(lll)electrodesurfaceswasstudiedbyboth voltammetry and in situ infrared reflection absorption spectroscopy. The terminal hydrogens adsorbed on Pt( 100)) Pt ( 11 1 1) and Pt( 110) electrodes were observed at 1990-2080 cm-' as bands appearing at potentials more negative than 0.25,O.l and 0 V versus SHE, respectively. However, a well-oriented pt ( 111) electrode did not give a significant absorption of the terminal hydrogens under similar conditions. The terminal hydrogen adsorption was sensitive to the surface crystallographic orientation.
๐ SIMILAR VOLUMES
The reconstruction process on a clean Pt ( 110) surface was monitored by infrared reflection absorption spectra of CO on the surface. The adsorbate-induced phase transition from the (1 x2 )-Pt (110) to the ( I x I )-Pt( 110) structure was completely suppressed under negative electrode potentials. Th
At least two different solution species were adsorbed on a Pt(l I 1) electrode in acid solutions; one is neutral H 20, and the other the hydronium ion H3 O+. The former neutral molecule chemisorbed through an oxygen lone pair to a hydrogen covered platinum surface. At potentials more positive than 0