Neutralization of Li+ ions scattered by the Cu (100) and (111) surfaces: A localized picture of the atom-surface interaction

被引:28
作者
Garcia, Evelina A. [1 ]
Romero, M. A. [1 ]
Gonzalez, C. [2 ]
Goldberg, E. C. [1 ,3 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, Inst Desarrollo Tecnol Ind Quim INTEC, RA-3000 Santa Fe, Argentina
[2] Acad Sci Czech Republ, Inst Phys, Dept Thin Films, Prague 16253, Czech Republic
[3] Univ Nacl Litoral, Fac Ingn Quim, Dept Ing Mat, RA-3000 Santa Fe, Argentina
关键词
Charge transfer; Alkali metals; Electron transfer; Neutralization mechanisms; Atom-solid interaction; RESONANT CHARGE-TRANSFER; PROJECTED BAND-GAP; STATE; ALKALI/AL(100); COLLISIONS; DYNAMICS; EXCHANGE; SHIFTS;
D O I
10.1016/j.susc.2008.12.022
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
Large and face dependent neutral fractions have been found recently in the scattering of Li+ by Cu(100) and Cu(111) surfaces. These results for high work function surfaces are unexpected within the 'traditional' picture of a Li+ ion departing from a jellium surface model. In the present work the Li+/Cu(100) and Li+/Cu(111) interacting systems are described by a previously developed bond-pair model based on the localized interactions between the projectile ion and the atoms of the surface, and on the extended features of the electronic band structure through the surface local density of states. By only including the resonant neutralization to the Li atom ground state we explained the face and energy dependences of the measured neutral fractions for large outgoing energy values. We found that the downward shift of the Li ionization level below the Fermi level caused by the short range chemical interactions, is the main responsible of a high neutralization by the resonant mechanism. The remaining differences between theory and experiment values can be explained in terms of the energy gaps and image potential states appearing in these surfaces. The calculated distance behaviours of the energy levels corresponding to the first excited (U-1s(2)2p) and the negative (Li-1s(2)2s(2)) atomic configurations indicate that they can also participate in the ion-surface charge exchange process. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:597 / 605
页数:9
相关论文
共 43 条
[1]   CHARGE-EXCHANGE PROCESSES IN LI+ AND HE+ ION-SCATTERING FROM ALKALI ADSORBATES ON CU(110) [J].
ASHWIN, MJ ;
WOODRUFF, DP .
SURFACE SCIENCE, 1991, 244 (03) :247-258
[2]   Charge transfer in hyperthermal energy collisions of Li+ with alkali-metal-covered Cu(001) .1. Dynamics of charge state formation [J].
Behringer, ER ;
Andersson, DR ;
Cooper, BH ;
Marston, JB .
PHYSICAL REVIEW B, 1996, 54 (20) :14765-14779
[3]   REVIEW OF TECHNIQUES IN THE LARGE-N EXPANSION FOR DILUTE MAGNETIC-ALLOYS [J].
BICKERS, NE .
REVIEWS OF MODERN PHYSICS, 1987, 59 (04) :845-939
[5]   Interaction between atoms and surfaces: A bond-pair description based on an extended Anderson model [J].
Bolcatto, PG ;
Goldberg, EC ;
Passeggi, MCG .
PHYSICAL REVIEW B, 1998, 58 (08) :5007-5021
[6]   Relevant effects of localized atomic interactions and surface density of states on charge transfer in ion-surface collisions [J].
Bonetto, F. ;
Romero, M. A. ;
Garcia, E. A. ;
Vidal, R. ;
Ferron, J. ;
Goldberg, E. C. .
EPL, 2007, 80 (05)
[7]   Large neutral fractions in collisions of Li+ with a highly oriented pyrolytic graphite surface:: Resonant and Auger mechanisms [J].
Bonetto, F. ;
Romero, M. A. ;
Garcia, Evelina A. ;
Vidal, R. A. ;
Ferron, J. ;
Goldberg, E. C. .
PHYSICAL REVIEW B, 2008, 78 (07)
[8]   Finite time effect in the charge transfer process during an ion-metal surface collision [J].
Borisov, AG ;
Kazansky, AK ;
Gauyacq, JP .
PHYSICAL REVIEW LETTERS, 1998, 80 (09) :1996-1999
[9]   Resonant charge transfer in ion-metal surface collisions:: Effect of a projected band gap in the H--Cu(111) system [J].
Borisov, AG ;
Kazansky, AK ;
Gauyacq, JP .
PHYSICAL REVIEW B, 1999, 59 (16) :10935-10949
[10]   Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface [J].
Borisov, AG ;
TeilletBilly, D ;
Gauyacq, JP ;
Winter, H ;
Dierkes, G .
PHYSICAL REVIEW B, 1996, 54 (23) :17166-17174