Interlayer reconstruction phase transition in van der Waals materials

IF 38.5 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Junwei Zhang, Laiyuan Wang, Jingtao Lü, Zhe Wang, Huan Wu, Guilin Zhu, Nan Wang, Fei Xue, Xue Zeng, Liu Zhu, Yang Hu, Xia Deng, Chaoshuai Guan, Chen Yang, Zhaoyang Lin, Peiqi Wang, Boxuan Zhou, Jing Lü, Wenguang Zhu, Xixiang Zhang, Yu Huang, Wei Huang, Yong Peng, Xiangfeng Duan
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引用次数: 0

Abstract

Van der Waals materials display rich structural polymorphs with distinct physical properties. An atomistic understanding of the phase-transition dynamics, propagation pathway and associated evolution of physical properties is essential for capturing their potential in practical technologies. However, direct visualization of the rapid phase-transition process is fundamentally challenging due to the inherent trade-offs among atomic resolution, field of view and imaging frame rate. Here we exploit a controllable current-driven phase transition and utilize in situ scanning transmission electron microscopy to visualize dynamic atomic rearrangements during the 2H-α to 2H-β transition in layered In2Se3. We identify a unique intralayer-splitting (unzipping) and interlayer-reconstruction (zipping) pathway, driven by an energy-cascading mechanism through which bond formation across the van der Waals gap facilitates bond cleavage in the covalent layers. We also observe current-direction-dependent asymmetric phase-transition propagation and attribute it to a temperature profile induced by the Peltier effect at the heterophase interface. These findings provide insights that are essential for designing tailored structural phase transitions in advanced technologies. Current-driven dynamic atomic rearrangements in layered In2Se3 are visualized. The authors identify an intralayer ‘unzipping’ and interlayer ‘zipping’ phase-transition pathway in which bond formation across the van der Waals gaps drives bond cleavage within covalent layers.

Abstract Image

Abstract Image

范德华材料的层间重构相变
范德华材料表现出丰富的结构多晶,具有独特的物理性质。从原子的角度理解相变动力学、传播途径和物理性质的相关演变,对于捕捉它们在实际技术中的潜力至关重要。然而,由于原子分辨率、视场和成像帧率之间的内在权衡,快速相变过程的直接可视化从根本上具有挑战性。在这里,我们利用可控的电流驱动相变,并利用原位扫描透射电子显微镜来观察层状In2Se3中2H-α到2H-β转变过程中的动态原子重排。我们确定了一种独特的层内分裂(unzipping)和层间重建(zipping)途径,由能量级联机制驱动,通过该机制,跨越范德华间隙的键形成促进了共价层中的键裂解。我们还观察到电流方向相关的不对称相变传播,并将其归因于异相界面上由珀尔帖效应引起的温度分布。这些发现为在先进技术中设计量身定制的结构相变提供了至关重要的见解。
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来源期刊
Nature Materials
Nature Materials 工程技术-材料科学:综合
CiteScore
62.20
自引率
0.70%
发文量
221
审稿时长
3.2 months
期刊介绍: Nature Materials is a monthly multi-disciplinary journal aimed at bringing together cutting-edge research across the entire spectrum of materials science and engineering. It covers all applied and fundamental aspects of the synthesis/processing, structure/composition, properties, and performance of materials. The journal recognizes that materials research has an increasing impact on classical disciplines such as physics, chemistry, and biology. Additionally, Nature Materials provides a forum for the development of a common identity among materials scientists and encourages interdisciplinary collaboration. It takes an integrated and balanced approach to all areas of materials research, fostering the exchange of ideas between scientists involved in different disciplines. Nature Materials is an invaluable resource for scientists in academia and industry who are active in discovering and developing materials and materials-related concepts. It offers engaging and informative papers of exceptional significance and quality, with the aim of influencing the development of society in the future.
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