Phase transformation via atomic-scale periodic interfacial energy

被引:0
|
作者
Cui, Ye [1 ]
Zhang, Yang [1 ]
Sun, Lixin [1 ]
Feygenson, Mikhail [2 ]
Fan, Mingyu [1 ]
Wang, Xun-Li [3 ]
Liaw, Peter K. [4 ]
Baker, Ian [5 ]
Zhang, Zhongwu [1 ]
机构
[1] Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin, Engineering University, Harbin,150001, China
[2] Forschungszentrum Jülich GmbH, Jülich Centre for Neutron Science (JCNS-1) and Biological Matter (IBI-8), Jülich,52425, Germany
[3] Department of Physics, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong
[4] Department of Materials Science and Engineering, The University of Tennessee, Knoxville,TN,37996-2100, United States
[5] Thayer School of Engineering, Dartmouth College, 14 Engineering Drive, Hanover,NH,03755, United States
来源
Materials Today Physics | 2022年 / 24卷
基金
中国国家自然科学基金; 中国博士后科学基金; 美国国家科学基金会;
关键词
Phase transitions - Atoms - Lithium alloys;
D O I
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摘要
Displacive and diffusional transformations are the main processes during solid-state phase transformations, which have formed the basis of applied physics and materials technology for centuries. However, the relationship between diffusional and displacive transformations has remained elusive, which significantly hinders the fundamental understanding and control of the microstructures and properties of materials via phase transformations. Here, we introduce the concept of a periodic differential interfacial energy between atom layers. We develop the mechanism of an atomic-scale displacive process in the form of atoms groups (cells) based on the periodic differential interfacial energy and experimentally determine the displacive short-range order (SRO) cell size in an Mg–Li alloy using a neutron total scattering method. We proposed that the origins of both the displacive and diffusional transformations are displacive in nature governed by the driving force of transformations. Our work paves the way for building a bridge correlating the nature of various solid-state phase transformations. © 2022 Elsevier Ltd
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