The growth of epitaxial VN(111) nanolayer surfaces

被引:22
作者
Glaser, A.
Surnev, S. [1 ]
Ramsey, M. G.
Lazar, P.
Redinger, J.
Podloucky, R.
Netzer, F. P.
机构
[1] Karl Franzens Univ Graz, Inst Phys Oberflachen & Grenzflachenphys, A-8010 Graz, Austria
[2] Vienna Univ Technol, Inst Allgemeine Phys, A-1060 Vienna, Austria
[3] Univ Vienna, Inst Phys Chem, A-1090 Vienna, Austria
关键词
vanadium nitride; photoelectron spectroscopy; density functional theory;
D O I
10.1016/j.susc.2007.07.032
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 [物理化学]; 081704 [应用化学];
摘要
Ultrathin films of vanadium nitride (1-20 monolayers = nanolayers) with (I 11) orientation have been grown on a Pt(111) surface by reactive evaporation of vanadium in NH3 atmosphere. The VN(111) surfaces have been investigated by X-ray and UV photoelectron spectroscopy, LEED, work function measurements, and ab initio DFT calculations. Nearly stoichiometric, well-ordered VN0.9 overlayers with their (1 x 1) unit cells rotationally aligned to the high symmetry directions of the Pt substrate have been obtained after annealing the films deposited at 300-500 degrees C in vacuum. The experimental valence band spectra have been compared to the theoretical density of states for differently terminated VN(111) surfaces, i.e. V and N terminated surfaces, bare and with chemisorbed hydrogen. The comparison suggests that the VN(111) nanolayers are terminated by a hexagonal layer of vanadium atoms, possibly covered with some chemisorbed hydrogen (which may originate from the preparation procedure). The VN nanolayer growth on Pt(111) follows a S trans ki-Krastanov layer-plus-island growth mode. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:4817 / 4823
页数:7
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