Reactive scattering study of etching dynamics:: Cl2 on GaAs(100)

被引:17
作者
Bond, P [1 ]
Prier, PN [1 ]
Fletcher, J [1 ]
Jia, WJ [1 ]
Price, H [1 ]
Gorry, PA [1 ]
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
chemisorption; chlorine; etching; gallium arsenide; molecule-solid scattering and diffraction inelastic; molecule-solid reactions; physical adsorption; surface chemical;
D O I
10.1016/S0039-6028(98)00715-8
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
Pulsed supersonic molecular beam scattering has been used to study of the inelastic scattering, trapping desorption and reactive channels for the Cl-2 + GaAs(100) thermal etching reactions. Temperature profiles of the reactive products GaCl, GaCl3, AsCl3, As-4 and As-2 are reported in the rang 340 to 825 K. Angular and time-of-flight (TOF) distributions of inelastically scattered and trapped + desorbed Cl-2 are also reported. The translational inelasticity has been measured as a function of final scattering angle at two initial translational energies, 18 and 53.4 kJ mol(-1). Angular distribution of all reaction products are described by a cos(n)(theta) form with 1.1 less than or equal to n less than or equal to 1.3. The TOF distributions of GaCl, GaCl3 and AsCl3 reveal prompt production but with measurable time delays (50 mu s-5 ms). The As-4 and As-2 signals are effectively demodulated and correspond to delayed production on the surface with a time constant >1 s. The surface time profiles for GaCl and GaCl3 are each well described by double-exponential decays for production desorption from the surface. The temperature dependence of the time constants for each product yield pairs of Arrhenius plots with common activation energies but different pre-exponential factors. It is argued that these do not correspond to two separate processes but reflect single product desorption with a coverage-dependent activation energy. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 209
页数:29
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