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直接观察中熵合金中的化学短程有序。

Direct observation of chemical short-range order in a medium-entropy alloy.

机构信息

State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing, China.

School of Engineering Science, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Nature. 2021 Apr;592(7856):712-716. doi: 10.1038/s41586-021-03428-z. Epub 2021 Apr 28.

DOI:10.1038/s41586-021-03428-z
PMID:33911276
Abstract

Complex concentrated solutions of multiple principal elements are being widely investigated as high- or medium-entropy alloys (HEAs or MEAs), often assuming that these materials have the high configurational entropy of an ideal solution. However, enthalpic interactions among constituent elements are also expected at normal temperatures, resulting in various degrees of local chemical order. Of the local chemical orders that can develop, chemical short-range order (CSRO) is arguably the most difficult to decipher and firm evidence of CSRO in these materials has been missing thus far. Here we discover that, using an appropriate zone axis, micro/nanobeam diffraction, together with atomic-resolution imaging and chemical mapping via transmission electron microscopy, can explicitly reveal CSRO in a face-centred-cubic VCoNi concentrated solution. Our complementary suite of tools provides concrete information about the degree/extent of CSRO, atomic packing configuration and preferential occupancy of neighbouring lattice planes/sites by chemical species. Modelling of the CSRO order parameters and pair correlations over the nearest atomic shells indicates that the CSRO originates from the nearest-neighbour preference towards unlike (V-Co and V-Ni) pairs and avoidance of V-V pairs. Our findings offer a way of identifying CSRO in concentrated solution alloys. We also use atomic strain mapping to demonstrate the dislocation interactions enhanced by the CSROs, clarifying the effects of these CSROs on plasticity mechanisms and mechanical properties upon deformation.

摘要

多种主要元素的复杂浓缩溶液作为高熵或中熵合金(HEA 或 MEA)得到了广泛的研究,通常假设这些材料具有理想溶液的高组态熵。然而,在常温下,组成元素之间也存在焓相互作用,导致局部化学有序程度不同。在可能出现的局部化学有序中,化学短程有序(CSRO)是最难解释的,到目前为止,这些材料中 CSRO 的确凿证据一直缺失。在这里,我们发现,使用适当的晶带轴、微/纳米束衍射,以及通过透射电子显微镜的原子分辨率成像和化学映射,可以明确揭示面心立方 VCoNi 浓缩溶液中的 CSRO。我们的一系列互补工具提供了关于 CSRO 程度/程度、原子堆积结构以及化学物质优先占据相邻晶格平面/位置的具体信息。对最近原子壳层上 CSRO 序参量和对关联的建模表明,CSRO 源自最近邻对异类(V-Co 和 V-Ni)对的偏好和对 V-V 对的回避。我们的发现为识别浓溶液合金中的 CSRO 提供了一种方法。我们还使用原子应变映射来证明 CSRO 增强的位错相互作用,阐明这些 CSRO 对变形时塑性机制和力学性能的影响。

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