Energy and site selectivity in O-atom photodesorption from nanostructured MgO

被引:23
作者
Beck, Kenneth M. [3 ]
Joly, Alan G. [3 ]
Diwald, Oliver [1 ]
Stankic, Slavica [4 ]
Trevisanutto, Paolo E. [2 ,5 ]
Sushko, Peter V. [2 ,6 ]
Shluger, Alexander L. [2 ,6 ]
Hess, Wayne P. [3 ]
机构
[1] Vienna Univ Technol, Inst Mat Chem, A-1210 Vienna, Austria
[2] UCL, Dept Phys & Astron, London Ctr Nanotechnol, Mat Simulat Lab, London WC1E 6BT, England
[3] Pacific NW Natl Lab, Richland, WA 99352 USA
[4] CNRS, Inst Nanosci Paris, F-75015 Paris, France
[5] CNRS, Inst Neel, Grenoble, France
[6] Tohoku Univ, WPI Adv Inst Mat Res, Sendai, Miyagi 980, Japan
基金
奥地利科学基金会;
关键词
density functional calculations; desorption induced by electronic transitions (DIET); photon stimulated desorption (PSD); atom emission; magnesium oxides; surface defects; excitons; laser control;
D O I
10.1016/j.susc.2008.03.046
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
We excite low-coordinated surface sites of nanostructured MgO samples using 4.7 eV UV laser pulses and observe dominant hyperthermal O-atom emission. Excitation of the same samples with 7.9 eV photons results in thermal O-atom desorption. These results are analyzed in the context of laser desorption models developed previously for alkali halide crystals and MgO. We detail two multi-step mechanisms for hyperthermal O-atom, desorption, under surface selective excitation, based on exciton and hole trapping at three-coordinated (corner) O-atom sites, and evaluate the validity of each based on available experimental data and calculated results. The proposed models are significantly different from and more complex than the surface exciton desorption model established for alkali halides. Nonetheless, the principles of site-specific photo-excitation and exciton and hole localization induced atomic desorption are clearly extendable to a prototypical metal oxide. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1968 / 1973
页数:6
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