Desorption induced by femtosecond laser pulses.
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Summary
The yield and final-state distributions in translational and internal degrees of freedom have been established for NO molecules desorbed from a Pd(111) surface by 200-fs pulses of 2.0-eV photons, indicating that a new desorption mechanism, distinct from either conventional thermal or photochemical processes, is operative in this regime.
- Type
- article
- Published
- 1990-03-26
- Cited by
- 208
- References
- 0
- OpenAlex
- https://openalex.org/W1985369839
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:46098973
Keywords
Desorption, Femtosecond, Nanosecond, Atomic physics, Laser
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Cited by
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- State- and Time-Resolved Investigations of Energy Transfer Mechanisms in Femtosecond-Laser induced Associative Desorption
- Photochemical transformations on plasmonic metal nanoparticles.
- Size-dependent photochemistry of NO dimers adsorbed on alumina supported silver nanoparticles
- Influencing laser-accelerated ions by femtosecond-laser desorption
- Photon-stimulated desorption from chlorinated Si(111): Etching of SiCl by picosecond-pulsed laser irradiation
- Femtosecond dynamics of electronic excitations at metal surfaces
- Vibrational excitation dynamics in photodesorption
- Velocity distributions of photochemically desorbed molecules
- Ro-vibrational excitation, alignment and orientation distributions of fast non-dissociatively scattered molecules
- A theoretical study of laser desorption of molecules induced by an ultrashort pulse
- Femtosecond quantum control of molecular bond formation
- Femtosecond laser desorption of CO from the Pt(111) surface
- Photodissociation of adsorbed Mo(CO)6 induced by direct photoexcitation and hot electron attachment. II. Physical mechanisms
- Adsorption and UV-induced dissociation of ClCH2CH2Br on Pt(111)
- Energy partitioning in the femtosecond-laser-induced associativeD2desorption from Ru(0001)
- Role of projectile-motion-induced electronic transitions in the dissociation of fast H2 at a Cu(111) surface
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