Synchrotron radiation photoemission and photostimulated desorption of deuterated methanol on Si(111)7x7 and Si(100)2x1

被引:34
作者
Carbone, M
Zanoni, R
Piancastelli, MN
Comtet, G
Dujardin, G
Hellner, L
机构
[1] UNIV ROMA TOR VERGATA,DEPT CHEM SCI & TECHNOL,I-00133 ROME,ITALY
[2] UNIV ROMA LA SAPIENZA,DEPT CHEM,I-00185 ROME,ITALY
[3] UNIV PARIS 11,UTILISAT RAYONNEMENT ELECTROMAGNET LAB,F-91405 ORSAY,FRANCE
[4] UNIV PARIS 11,PHOTOPHYS MOLEC LAB,F-91405 ORSAY,FRANCE
关键词
alcohols; photon stimulated desorption (PSD); semiconducting surfaces; single crystal surfaces; soft X-ray photoelectron spectroscopy; surface chemical reaction;
D O I
10.1016/0039-6028(95)01167-6
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
Deuterated methanol adsorption on Si(111)7 X 7 and Si(100)2 X 1 surfaces has been investigated, at room temperature, by synchrotron radiation photoemission and photostimulated desorption. Photoemission experiments as a function of methanol coverage show that deuterated methanol adsorption is dissociative on both surfaces and occurs via sigma(O-D) bond breakage and sigma(Si-O) bond formation. Site selectivity is displayed by the methoxy species on Si(111)7 X 7 surface, since the S-2 surface state related to the rest atoms is quickly quenched upon low coverage adsorption. The S-1 surface state is quenched only subsequently at much higher coverages. The photostimulated desorption pattern is similar for the two surfaces and strongly depends on the investigated energy range. D+ is always the most abundant ion produced, but higher mass fragments are present too in the energy range including the C 1s threshold, where multiple desorption processes are possibly taking place.
引用
收藏
页码:391 / 395
页数:5
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