CrI3/Br3Cr2I3 异质结构中的压力驱动磁性相变

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Subhan Fazle, Ali Luqman, Razia Aman, Ailing Chen, Bo Peng, Yanguang Zhou, Zhenzhen Qin, Guangzhao Qin
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引用次数: 0

摘要

垂直堆叠的范德瓦尔斯(vdW)异质结构不仅在能带排列方面提供了一个前景广阔的平台,而且还为基础科学的研究提供了肥沃的土壤,并对不同的设备应用产生了巨大的实际兴趣。大多数二维(2D)材料本质上都是无磁性的,而 CrI3 则是一种具有 vdW 键合层磁性的新型材料,具有潜在的自旋电子学应用前景。然而,为了实现突出的器件应用,通常需要制造异质结构,因此有必要研究界面或接触原子对异质结构磁性能的影响。最重要的是,组装应力对电子和磁性能的影响仍不清楚。在本研究中,我们设计了一种由双铬三卤化物构成的 vdW 异质结构,称为 CrI3/Br3Cr2I3 异质结构,其中 CrI3 单层的 Janus 称为 Br3Cr2I3,也是一种本征二维磁性材料。利用最先进的第一性原理计算,我们揭示了接触原子以及外部压力对 CrI3/Br3Cr2I3 异质结构的电子和磁性能的影响。研究发现,当压力大于一定阈值时,异质结构会从反铁磁(AFM)跃迁到铁磁(FM)基态。我们还研究了 CrI3/Br3Cr2I3 异质结构的磁晶各向异性能(MAE)。值得注意的是,我们发现磁晶各向异性能受堆叠原子和接触原子的影响都很大,而且受接触原子和外部压力的影响变化突然且不一致。此外,我们还揭示了 MAE 与极角之间的相关性。本研究揭示的 CrI3/Br3Cr2I3 异质结构的压力调节磁性能凸显了其在自旋电子应用设备中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pressure driven magnetic phase change in CrI3/Br3Cr2I3 heterostructure
The vertically stacked van der Waals (vdW) heterostructures provide a promising platform not only in the band alignment but also constitute a fertile ground for the fundamental science and tremendous practical interest towards different device applications. Beyond most two-dimensional (2D) materials being intrinsically non-magnetic, CrI3 is a novel material with vdW bonded layer dependent magnetism, promising the potential spintronics applications. However, for prominent device applications, heterostructure is commonly fabricated and it is necessary to examine the effect of the interface or contact atoms over the magnetic properties of the heterostructure. And most importantly, the effect of assembly stress on the electronic and magnetic properties remains not clear. In this study, we design a vdW heterostructure from the two-chromium tri-halides called CrI3/Br3Cr2I3 heterostructure, where the Janus of the CrI3 monolayer called Br3Cr2I3 is also an intrinsically 2D magnetic material. Using the state-of-the-art first principles calculations, we uncover the effects of contact atoms as well as external pressure over the electronic and magnetic properties of the CrI3/Br3Cr2I3 heterostructure. It is found that the heterostructure transits from antiferromagnetic (AFM) to ferromagnetic (FM) ground state with pressure larger than certain threshold. We also investigate the magneto-crystalline anisotropy energy (MAE) of the CrI3/Br3Cr2I3 heterostructure. Remarkably, it is found that the MAE is significantly influenced by both the stacking as well as the contact atoms, which is abruptly and inconsistently varying by the contact atoms and external pressure. Further, we also reveal the correlation between MAE and the polar angle. The pressure regulated magnetic properties of the CrI3/Br3Cr2I3 heterostructures as revealed in this study highlight its potential applications for spintronic applications devices.
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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