THE DYNAMICS OF PRECURSOR ADSORPTION - ETHANE ON PT(111)

被引:25
作者
ARUMAINAYAGAM, CR
MCMASTER, MC
MADIX, RJ
机构
[1] STANFORD UNIV,DEPT CHEM,STANFORD,CA 94305
[2] STANFORD UNIV,DEPT CHEM ENGN,STANFORD,CA 94305
关键词
D O I
10.1016/0039-6028(90)90514-9
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
We have studied ethane trapping into a second-layer state on Pt(111) using supersonic molecular beam techniques to investigate the dynamics of extrinsic precursor adsorption. Initial trapping probabilities of ethane on an ethane covered Pt(111) surface were measured directly as a function of incident translational energy and incident angle at a surface temperature of 95 K. At all incident translational energies and angles the initial trapping probability into the second-layer state is higher than on a clean surface. In addition the initial trapping probability into the second layer decreases less with incident translational energy than the initial trapping probability onto the clean surface. In contrast to previous findings for non-dissociative weak adsorption on clean surfaces showing the initial trapping probability to increase with incident angle, the initial trapping probability into the second layer is independent of incident angle indicating "total" energy scaling. A dynamical corrugation of the adsorbed layer is postulated to rationalize this strong deviation from the "normal" energy scaling implicit in one-dimensional theories of trapping. © 1990.
引用
收藏
页码:L424 / L431
页数:8
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