๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Polarization probe of excitation mechanisms in surface photochemistry

โœ Scribed by X.-Y. Zhu; J.M. White; M. Wolf; E. Hasselbrink; G. Ertl


Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
701 KB
Volume
176
Category
Article
ISSN
0009-2614

No coin nor oath required. For personal study only.

โœฆ Synopsis


Based on classical electrodynamic theory, cross sections for surface photochemical processes are derived as a function of the angle of incidence. Using s-and p-polarized light, the expected primary excitation mechanisms, i.e. direct excitation and substrate excitation, can be distinguished. Two examples are shown: for O2 on Pd( Ill), photo-induced desorption and dissociation at 6.4 eV are unambiguously due to substrate excitation, while for ClzCO on Pt ( 1 I I ), direct excitation plays an important role in photolysis at 4.4 eV.


๐Ÿ“œ SIMILAR VOLUMES


Excitation mechanisms in the photochemis
โœ M. Wolf; X.-Y. Zhu; J.M. White ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 469 KB

It is demonstrated that direct and substrate-mediated excitation mechanisms in surface photochemical reactions can be discriminated based on the pronounced angular dependence of the electric fields at the vacuum interface of a transparent substrate covered with a thin metal film. We can unambiguousl

Rotational excitation as a probe of phot
โœ Joseph W. Burnett; Mark A. Young ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 614 KB

Laser excitation in the range 280-285 nm was used to initiate chemistry in small (HI), clusters formed in a supersonicexpansion. The same laser pulse also probed the rotational population of HI monomers by 2 + 1 REMPI through three different excited states. An increase in the HI rotational temperatu

On the mechanism of rotational polarizat
โœ Jack G. Lauderdale; Joe F. Mcnutt; C.William McCurdy ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 497 KB

Quantum close-coupling c3Icuhtions are presented which verify that the rotational polartriution observed in recent experiments on NO-Ag(I 11) scattering is due primarily to rzv conservation. However a dramatic dependena of rotational transitions on initial q in some surfwe collisions is also indicat