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首页> 外文期刊>Journal of surface investigation: x-ray, synchrotron and neutron techniques >Nanoscale peculiarities of the thermally stimulated surface autosegregation of covalent crystals: Gallium arsenide
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Nanoscale peculiarities of the thermally stimulated surface autosegregation of covalent crystals: Gallium arsenide

机译:共价晶体的热激发表面自分离的纳米级特性:砷化镓

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摘要

Nanoscale changes in the morphology and elemental composition of cleavage surfaces of gallium arsenide crystals, which arise due to thermally stimulated surface autosegregation, are investigated in detail and systematized. It is shown that, depending on the annealing conditions (temperature, duration, and evacuation), gallium arsenide dissociates, forming submicron nonstoichiometric layers on the surface or local phases of arsenic, gallium, and gallium oxide. The mechanism and nature of autosegregation are determined by the competing processes of arsenic sublimation and its surface diffusion with an activation energy of ~31 kJ/mol. The migration of arsenic atoms is described with the help of a crystallochemical model. The nanomorphology of the surface phases includes arsenic and gallium nanoparticles with sizes of 10-200 nm, their agglomerates, and gallium oxide nano- and microcrystallites combined in plate- and chainlike configurations.
机译:详细研究并系统化了由于热激发的表面自偏析而导致的砷化镓晶体分裂表面的形态和元素组成的纳米级变化。结果表明,根据退火条件(温度,持续时间和抽真空),砷化镓离解,在砷,镓和氧化镓的表面或局部相上形成亚微米非化学计量层。自分离的机理和性质取决于砷的升华及其表面扩散的竞争过程,活化能约为31 kJ / mol。借助晶体化学模型描述了砷原子的迁移。表面相的纳米形态包括尺寸为10-200 nm的砷和镓纳米颗粒,它们的团聚体以及以板状和链状构型结合的氧化镓纳米微晶。

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