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确定非晶态固体的三维原子结构。

Determining the three-dimensional atomic structure of an amorphous solid.

机构信息

Department of Physics & Astronomy, STROBE NSF Science & Technology Center and California NanoSystems Institute, University of California, Los Angeles, CA, USA.

Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, P. R. China.

出版信息

Nature. 2021 Apr;592(7852):60-64. doi: 10.1038/s41586-021-03354-0. Epub 2021 Mar 31.

DOI:10.1038/s41586-021-03354-0
PMID:33790443
Abstract

Amorphous solids such as glass, plastics and amorphous thin films are ubiquitous in our daily life and have broad applications ranging from telecommunications to electronics and solar cells. However, owing to the lack of long-range order, the three-dimensional (3D) atomic structure of amorphous solids has so far eluded direct experimental determination. Here we develop an atomic electron tomography reconstruction method to experimentally determine the 3D atomic positions of an amorphous solid. Using a multi-component glass-forming alloy as proof of principle, we quantitatively characterize the short- and medium-range order of the 3D atomic arrangement. We observe that, although the 3D atomic packing of the short-range order is geometrically disordered, some short-range-order structures connect with each other to form crystal-like superclusters and give rise to medium-range order. We identify four types of crystal-like medium-range order-face-centred cubic, hexagonal close-packed, body-centred cubic and simple cubic-coexisting in the amorphous sample, showing translational but not orientational order. These observations provide direct experimental evidence to support the general framework of the efficient cluster packing model for metallic glasses. We expect that this work will pave the way for the determination of the 3D structure of a wide range of amorphous solids, which could transform our fundamental understanding of non-crystalline materials and related phenomena.

摘要

无定形固体,如玻璃、塑料和非晶薄膜,在我们的日常生活中无处不在,广泛应用于从电信到电子和太阳能电池等领域。然而,由于缺乏长程有序性,无定形固体的三维(3D)原子结构迄今仍无法通过实验直接确定。在这里,我们开发了一种原子电子断层扫描重建方法,用于实验确定无定形固体的 3D 原子位置。我们使用多组分玻璃形成合金作为原理证明,定量地表征了 3D 原子排列的短程和中程有序性。我们观察到,尽管短程有序的 3D 原子堆积在几何上是无序的,但一些短程有序结构相互连接,形成类似晶体的超团簇,并产生中程有序。我们在非晶样品中识别出四种类型的类似晶体的中程有序-面心立方、六方密堆积、体心立方和简单立方-共存,表现出平移但没有取向有序。这些观察结果为金属玻璃的有效团簇堆积模型的一般框架提供了直接的实验证据。我们期望这项工作将为广泛的无定形固体的 3D 结构的确定铺平道路,这将改变我们对非晶材料和相关现象的基本理解。

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