TOP-SITE ADSORPTION FOR K ON CU(111) AND NI(111) SURFACES

被引:59
作者
ADLER, DL
COLLINS, IR
LIANG, X
MURRAY, SJ
LEATHERMAN, GS
TSUEI, KD
CHABAN, EE
CHANDAVARKAR, S
MCGRATH, R
DIEHL, RD
CITRIN, PH
机构
[1] AT&T BELL LABS,MURRAY HILL,NJ 07974
[2] PENN STATE UNIV,DEPT PHYS,UNIV PK,PA 16802
[3] UNIV LIVERPOOL,INTERDISCIPLINARY RES CTR SURFACE SCI,LIVERPOOL L69 3BX,ENGLAND
[4] UNIV LIVERPOOL,DEPT PHYS,LIVERPOOL L69 3BX,ENGLAND
[5] BROOKHAVEN NATL LAB,DEPT PHYS,UPTON,NY 11973
[6] FOM,INST ATOM & MOLEC PHYS,1098 SJ AMSTERDAM,NETHERLANDS
来源
PHYSICAL REVIEW B | 1993年 / 48卷 / 23期
关键词
D O I
10.1103/PhysRevB.48.17445
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Surface-extended x-ray-absorption fine-structure (SEXAFS) measurements have been obtained from p (2 X 2) overlayers of K on Ni(111) and Cu(111) surfaces. The data show that at 65-70 K, potassium occupies the atop site on both substrates, with chemisorption bond lengths of 2.92+/-0.02 angstrom on Ni and 3.05+/-0.02 angstrom on Cu. The identical adsorption site and small change in bond length, only slightly larger than that predicted from the difference in Cu and Ni lattice constants, are consistent with the expected dominance of adatom-adatom interactions in these near-saturation metallic adlayers. The inability to obtain SEXAFS data from K at lower coverages on these surfaces and at these temperatures, indicative of disorder/multisite occupation, is further evidence of a relatively weak alkali-metal substrate interaction even in the dilute-adatom, nonmetallic-overlayer regime.
引用
收藏
页码:17445 / 17451
页数:7
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