The electrooxidation of CO adsorbate on well ordered Pt(ll1) surfaces is studied through a flow-cell technique. Potentiodynamic sweeps and potential steps are used to characterize the kinetic behaviour of the adsorbate. The effect of surface disturbance when the electrode is cycled into the oxide fo
Surface femtochemistry of 02 and CO on Pt(111)
β Scribed by S. Deliwala; R.J. Finlay; J.R. Goldman; T.H. Her; W.D. Mieher; E. Mazur
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 547 KB
- Volume
- 242
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Desorption of 0, and formation of CO, were induced with subpicosecond laser pulses on a Pt(ll1) surface dosed with coadsorbed 0, and CO. We report the fluence dependent yields obtained over a range of laser wavelengths from 267 to 800 nm, and pulse durations from 80 fs to 3.6 ps. The nonlinear dependence of the yield on fluence is different at different wavelengths. Two-pulse correlation measurements show two different time-scales relevant to the desorption. The results show that nonthermalized electrons play a role in the surface chemistry, and that an equilibrated pre-heating of the surface modes leads to enhanced desorption.
' UT1 1oOC operating in pulse counting mode.
π SIMILAR VOLUMES
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