Modification of the Shockley-type surface state on Ag(111) by an adsorbed xenon layer

被引:69
作者
Hövel, H [1 ]
Grimm, B [1 ]
Reihl, B [1 ]
机构
[1] Univ Dortmund, Otto Hahn Str, D-44221 Dortmund, Germany
关键词
scanning tunneling spectroscopies; scanning tunneling microscopy; angle resolved photoemission; surface electronic phenomena (work function; surface potential; surface states; etc.); physical adsorption; silver; noble gases; low index single crystal surfaces;
D O I
10.1016/S0039-6028(01)00704-X
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 Shockley-type surface state for the clean and a Xe covered Ag(111) surface is studied with scanning tunneling microscopy and scanning tunneling spectroscopy at a temperature of 5 It. The minimum of the parabolic dispersion shifts from -67 meV below E-r = 0 for the clean Ag(1 1 1) surface to +52 meV with one layer of Xe adsorbed, hence the surface slate becomes completely unoccupied after Xe adsorption. The dispersion is determined by measuring energy-dependent, locally-resolved, tunneling spectroscopy maps. These show standing wave patterns as local density of states formed by electron scattering at surface steps, which reveal equal effective masses with and without the Xe layer adsorbed. A line width analysis of the energetic onset of the surface state gives a slightly smaller lifetime of the surface state after Xe adsorption, in sharp contrast to the results for image states. We discuss the results and conclude that the wavefunction of the Shockley-type surface state stays close to the metal surface also after Xe adsorption. and that the observed shifts cannot be explained by the simultaneous change of the workfunction, but will be given mainly by the changes of the surface potential on an atomic scale. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 33 条
[1]   THE UNDERLAYER INFLUENCE ON PHOTOEMISSION AND THERMAL-DESORPTION OF XENON ADSORBED ON AG(111) [J].
BEHM, RJ ;
BRUNDLE, CR ;
WANDELT, K .
JOURNAL OF CHEMICAL PHYSICS, 1986, 85 (02) :1061-1073
[2]   ONE-DIMENSIONAL AND 2-DIMENSIONAL SURFACE-STATES ON METALS [J].
BERTEL, E .
SURFACE SCIENCE, 1995, 331 (pt B) :1136-1146
[3]   Tailoring surface electronic properties to promote chemical reactivity [J].
Bertel, E ;
Sandl, P ;
Rendulic, KD ;
Beutl, M .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1996, 100 (02) :114-118
[4]   THEORY OF THE LOCAL DENSITY OF SURFACE-STATES ON A METAL - COMPARISON WITH SCANNING TUNNELING SPECTROSCOPY OF A AU(111) SURFACE [J].
DAVIS, LC ;
EVERSON, MP ;
JAKLEVIC, RC ;
SHEN, WD .
PHYSICAL REVIEW B, 1991, 43 (05) :3821-3830
[5]   SPIN-DEPENDENT ELECTRONIC-STRUCTURE AT MAGNETIC-SURFACES - THE LOW-MILLER-INDEX SURFACES OF NICKEL [J].
DONATH, M .
SURFACE SCIENCE REPORTS, 1994, 20 (5-6) :251-316
[6]   EXISTENCE AND DETECTION OF RYDBERG STATES AT SURFACES [J].
ECHENIQUE, PM ;
PENDRY, JB .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1978, 11 (10) :2065-2075
[7]  
Ertl G., 1985, LOW ENERGY ELECT SUR
[8]   OBSERVATION OF SURFACE-STATES AT THE METAL ELECTROLYTE INTERFACE BY ELECTROREFLECTANCE SPECTROSCOPY [J].
HO, KM ;
FU, CL ;
LIU, SH ;
KOLB, DM ;
PIAZZA, G .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1983, 150 (1-2) :235-240
[9]   Time-resolved coherent spectroscopy of surface states [J].
Höfer, U .
APPLIED PHYSICS B-LASERS AND OPTICS, 1999, 68 (03) :383-392
[10]   IMAGING OF THE CU(111) SURFACE-STATE IN SCANNING-TUNNELING-MICROSCOPY [J].
HORMANDINGER, G .
PHYSICAL REVIEW B, 1994, 49 (19) :13897-13905