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纳米线液固极性界面处的3D有序排列。

3D Ordering at the Liquid-Solid Polar Interface of Nanowires.

作者信息

Zamani Mahdi, Imbalzano Giulio, Tappy Nicolas, Alexander Duncan T L, Martí-Sánchez Sara, Ghisalberti Lea, Ramasse Quentin M, Friedl Martin, Tütüncüoglu Gözde, Francaviglia Luca, Bienvenue Sebastien, Hébert Cécile, Arbiol Jordi, Ceriotti Michele, Fontcuberta I Morral Anna

机构信息

Laboratory of Semiconductor Materials, Institute of Materials, Faculty of Engineering, École Polytechnique Fédérale de Lausanne, EPFL, Lausanne, 1015, Switzerland.

Laboratory of Computational Science and Modeling, Institute of Materials, Faculty of Engineering, École Polytechnique Fédérale de Lausanne, EPFL, Lausanne, 1015, Switzerland.

出版信息

Adv Mater. 2020 Sep;32(38):e2001030. doi: 10.1002/adma.202001030. Epub 2020 Aug 6.

Abstract

The nature of the liquid-solid interface determines the characteristics of a variety of physical phenomena, including catalysis, electrochemistry, lubrication, and crystal growth. Most of the established models for crystal growth are based on macroscopic thermodynamics, neglecting the atomistic nature of the liquid-solid interface. Here, experimental observations and molecular dynamics simulations are employed to identify the 3D nature of an atomic-scale ordering of liquid Ga in contact with solid GaAs in a nanowire growth configuration. An interplay between the liquid ordering and the formation of a new bilayer is revealed, which, contrary to the established theories, suggests that the preference for a certain polarity and polytypism is influenced by the atomic structure of the interface. The conclusions of this work open new avenues for the understanding of crystal growth, as well as other processes and systems involving a liquid-solid interface.

摘要

液固界面的性质决定了包括催化、电化学、润滑和晶体生长在内的各种物理现象的特征。大多数已建立的晶体生长模型基于宏观热力学,忽略了液固界面的原子本质。在此,通过实验观察和分子动力学模拟来确定在纳米线生长构型中与固体砷化镓接触的液态镓的原子尺度有序排列的三维性质。揭示了液体有序排列与新双层形成之间的相互作用,这与现有理论相反,表明对特定极性和多型性的偏好受界面原子结构的影响。这项工作的结论为理解晶体生长以及其他涉及液固界面的过程和系统开辟了新途径。

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