Time-resolved femtosecond laser-induced desorption from magnesium oxide and lithium fluoride single crystals

被引:7
作者
Beck, KM [1 ]
Joly, AG [1 ]
Hess, WP [1 ]
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
laser methods; magnesium oxide; radiation damage; single crystal surfaces;
D O I
10.1016/S0039-6028(00)00023-6
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 have used the pump-probe technique to measure the photostimulated positive-ion yield, as a function of time delay, between two ultraviolet laser pulses. We find that the ion yield from 265 nm femtosecond-irradiated MgO and LiF depends critically on the laser pulse delay in two-pulse correlation experiments. For example, single-pulse excitation of MgO produces a variety of ions including Mg+, MgO+ and H+. If the femtosecond laser pulse is split into two sub-threshold beams and then recombined with a variable time delay, the Mg+ desorption yield displays three distinct time regimes and persists for laser delays of over 100 ps. A pulse delay of only 500 fs nearly eliminates ion desorption except for Mg+. In contrast, the Li+ desorption yield from LiF decays more rapidly, largely within the femtosecond pulse duration. A weak but measurable decay component of approximately 2 ps is indicated, however. We hypothesize that non-resonant excitation contributes to the ultrafast desorption mechanism, possibly through the creation of surface electron-hole pairs and allows direct observation of the surface dynamics. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:166 / 173
页数:8
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