H2O-INDUCED QUENCHING OF THE NEGATIVE-ION RESONANCE SCATTERING FOR N2 PHYSISORBED ON AL(111)

被引:22
作者
JACOBI, K
BERTOLO, M
GENG, P
HANSEN, W
ASTALDI, C
机构
[1] Fritz-Haber-Institut der Max-Planck-Gesellschaft, D-1000 Berlin 33
关键词
D O I
10.1016/0009-2614(90)85310-9
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
Monolayers of N2 physisorbed on the Al(111) surface at 20 K, were investigated by means of high-resolution electron energy-loss spectroscopy (HREELS) and UV photoelectron spectroscopy (UPS). The N2 stretching vibration at 290 meV is excited by negative-ion resonance scattering. By coadsorption of a 0.16 monolayer of H2O, the N2 stretching mode is strongly suppressed. This is explained as due to a complete quenching of the negative-ion resonance of N2 by the H2O molecules. © 1990.
引用
收藏
页码:97 / 102
页数:6
相关论文
共 26 条
[2]   ADSORPTION OF WATER MONOMERS ON CU(100) AND PD(100) AT LOW-TEMPERATURES [J].
ANDERSSON, S ;
NYBERG, C ;
TENGSTAL, CG .
CHEMICAL PHYSICS LETTERS, 1984, 104 (04) :305-310
[3]  
Bendtsen J., 1974, Journal of Raman Spectroscopy, V2, P133, DOI 10.1002/jrs.1250020204
[4]   THE ADSORPTION AND THERMAL-DECOMPOSITION OF WATER ON CLEAN AND OXYGEN-PREDOSED AL(111) [J].
CROWELL, JE ;
CHEN, JG ;
HERCULES, DM ;
YATES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (10) :5804-5815
[5]   THEORY OF VIBRATIONALLY INELASTIC ELECTRON-SCATTERING FROM ORIENTED MOLECULES [J].
DAVENPORT, JW ;
HO, W ;
SCHRIEFFER, JR .
PHYSICAL REVIEW B, 1978, 17 (08) :3115-3127
[6]   RESONANCE SCATTERING OF ELECTRONS FROM N-2, CO, O-2, AND H-2 ADSORBED ON A SILVER SURFACE [J].
DEMUTH, JE ;
SCHMEISSER, D ;
AVOURIS, P .
PHYSICAL REVIEW LETTERS, 1981, 47 (16) :1166-1169
[7]   GROWTH AND ELECTRONIC-STRUCTURE OF ULTRA-THIN PD AND AG FILMS ON AL(111) [J].
FRICK, B ;
JACOBI, K .
SURFACE SCIENCE, 1986, 178 (1-3) :907-916
[8]  
GADZUK JW, 1988, ANNU REV PHYS CHEM, V39, P395
[10]   PHYSISORPTION OF N-2 AND CO ON AL(111) - A COMBINED HREELS UPS INVESTIGATION [J].
JACOBI, K ;
ASTALDI, C ;
GENG, P ;
BERTOLO, M .
SURFACE SCIENCE, 1989, 223 (03) :569-577