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纳米小面的原子台阶流。

Atomic Step Flow on a Nanofacet.

机构信息

Centre de Nanosciences et de Nanotechnologies, CNRS, Université Paris-Sud, Université Paris-Saclay, Avenue de la Vauve, 91120 Palaiseau, France.

Laboratoire de Physique des Interfaces et des Couches Minces, Ecole polytechnique, CNRS, Université Paris-Saclay, 91128 Palaiseau, France.

出版信息

Phys Rev Lett. 2018 Oct 19;121(16):166101. doi: 10.1103/PhysRevLett.121.166101.

Abstract

Crystal growth often proceeds by atomic step flow. When the surface area available for growth is limited, the nucleation and progression of the steps can be affected. This issue is particularly relevant to the formation of nanocrystals. We examine the case of Au-catalyzed GaAs nanowires, which we grow in a transmission electron microscope. Our in situ observations show that atomic layers nucleate at the periphery of the interface between the nanowire and the catalyst droplet. From this starting location, the atomic step flows within a restricted area of hexagonal shape. At specific partial coverages, the monolayer configuration changes abruptly. A simple model based on the geometry of the system and its edge energies explains these observations. In particular, we observe an inversion of the step curvature which reveals that the effective energy per unit length of monolayer edge is much lower at the interface periphery than inside the catalyst droplet.

摘要

晶体生长通常通过原子台阶流进行。当可用的生长表面积有限时,晶核的形成和台阶的推进可能会受到影响。这个问题对于纳米晶体的形成尤为重要。我们研究了 Au 催化 GaAs 纳米线的情况,我们在透射电子显微镜中生长这种纳米线。我们的原位观察表明,原子层在纳米线和催化剂液滴之间的界面的外围处形核。从这个起始位置,原子台阶在六边形的受限区域内流动。在特定的部分覆盖度下,单层结构会突然发生变化。一个基于系统几何形状和边缘能的简单模型解释了这些观察结果。特别是,我们观察到台阶曲率的反转,这表明在催化剂液滴内部,单层边缘的单位长度有效能量比界面外围低得多。

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