PHOTOCHEMISTRY OF ADSORBED MOLECULES .6. ULTRAVIOLET PHOTOREACTION OF OCS ON LIF(001)

被引:31
作者
DIXONWARREN, SJ
LEGGETT, K
MATYJASZCZYK, MS
POLANYI, JC
YOUNG, PA
机构
[1] Department of Chemistry, University of Toronto, Toronto
[2] Department of Chemistry, University of Pennsylvania, Philadelphia
[3] Pylon Electronic Development Co. Ltd., Ottawa
[4] Ontario Centre for Materials Research, Interface Science and Technology, University of Western Ontario, London
关键词
D O I
10.1063/1.458796
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The surface-aligned photoreaction (PRXN) of OCS physisorbed on LiF(001) was investigated at 222 nm. Ultraviolet PRXN within the adsorbate was detected over a wide range of coverages. Diatomic sulphur was produced by reaction of photolytically generated sulphur atoms with a coadsorbed OCS molecule: S*, S + OCS(ad) →S2*, S2(g) + CO(ad/g). Translational energy and angular distributions of the S2 reaction product were obtained by angle-resolved time-of-flight mass spectrometry. The dynamics of PRXN were found to vary with adsorbate coverage. At low coverages (<10-2 ML), reaction was attributed to a "direct" abstraction mechanism, leading to energetic S2. As the coverage was increased above 10-2 ML, both "direct" and "indirect" PRXN dynamics were observed. Possible origins of these differing photoreaction dynamics are discussed. © 1990 American Institute of Physics.
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页码:3659 / 3672
页数:14
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