Paper
25 September 1995 Femtosecond laser activation of surface reactions
Richard J. Finlay, Shrenik M. Deliwala, Jay R. Goldman, Tsing-Hua Her, Walter D. Mieher, C. Wu, Eric Mazur
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Abstract
Laser induced formation of CO2 and desorption of O2 are initiated with femtosecond and picosecond laser excitation of a Pt(111) surface prepared with coadsorbed CO and O2 at 90 K. The nonlinear fluence dependent reaction yields were measured for 267, 400, and 800 nm wavelengths, and for pulse durations from 80 fs to 3.6 ps. Two-pulse correlation experiments measuring total O2 desorption yield versus time delay between 80 fs pulses show a 0.9 ps HWHM central peak and a slower 0.1 ns time-scale. At 267 nm the relative yields of O2 and CO2 are found to depend on fluence. Comparison of results at different wavelengths and pulsewidths shows that nonthermalized surface electrons play a role in the laser-induced surface chemistry.
© (1995) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Richard J. Finlay, Shrenik M. Deliwala, Jay R. Goldman, Tsing-Hua Her, Walter D. Mieher, C. Wu, and Eric Mazur "Femtosecond laser activation of surface reactions", Proc. SPIE 2547, Laser Techniques for Surface Science II, (25 September 1995); https://doi.org/10.1117/12.221499
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Cited by 4 scholarly publications.
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KEYWORDS
Electrons

Picosecond phenomena

Carbon dioxide

Carbon dioxide lasers

Pulsed laser operation

Platinum

Femtosecond phenomena

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