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通过超快光学激发对-WTe中堆叠顺序的操控。

Manipulation of Stacking Order in -WTe by Ultrafast Optical Excitation.

作者信息

Ji Shaozheng, Grånäs Oscar, Weissenrieder Jonas

机构信息

Materials and Nano Physics, School of Engineering Sciences, KTH Royal Institute of Technology, SE-100 44 Stockholm, Sweden.

Division for Materials Theory, Department of Physics and Astronomy, Uppsala University, SE-751 20 Uppsala, Sweden.

出版信息

ACS Nano. 2021 May 25;15(5):8826-8835. doi: 10.1021/acsnano.1c01301. Epub 2021 Apr 29.

Abstract

Subtle changes in stacking order of layered transition metal dichalcogenides may have profound influence on the electronic and optical properties. The intriguing electronic properties of -WTe can be traced to the break of inversion symmetry resulting from the ground-state stacking sequence. Strategies for perturbation of the stacking order are actively pursued for intentional tuning of material properties, where optical excitation is of specific interest since it holds the potential for integration of ultrafast switches in future device designs. Here we investigate the structural response in -WTe following ultrafast photoexcitation by time-resolved electron diffraction. A 0.23 THz shear phonon, involving layer displacement along the axis, was excited by a 515 nm laser pulse. Pump fluences in excess of a threshold of ∼1 mJ/cm result in formation, with an ∼5 ps time constant, of a new stacking order by layer displacement along the axis in the direction toward the centrosymmetric 1* phase. The shear displacement of the layers increases with pump fluence until saturation at ∼8 pm. We demonstrate that the excitation of the shear phonon and the stabilization of the metastable phase are decoupled when using an optical pump as evidenced by observation of a transition also in samples with a pinned shear phonon. The results are compared to dynamic first-principles simulations and the transition is interpreted in terms of a mechanism where transient local disorder is prominent before settling at the atomic positions of the metastable phase. This interpretation is corroborated by results from diffuse scattering. The correlation between excitation of intralayer vibrations and interlayer interaction demonstrates the importance of including both short- and long-range interactions in an accurate description of how optical fields can be employed to manipulate the stacking order in 2-dimensional transition metal dichalcogenides.

摘要

层状过渡金属二硫属化物堆叠顺序的细微变化可能会对电子和光学性质产生深远影响。-WTe引人入胜的电子性质可追溯到基态堆叠序列导致的反演对称性破缺。人们积极探索扰动堆叠顺序的策略,以有意调整材料性质,其中光激发特别受关注,因为它在未来器件设计中具有集成超快开关的潜力。在这里,我们通过时间分辨电子衍射研究了-WTe在超快光激发后的结构响应。一个0.23太赫兹的剪切声子,涉及沿轴的层位移,由一个515纳米的激光脉冲激发。超过约1毫焦/平方厘米阈值的泵浦通量会导致形成一种新的堆叠顺序,其时间常数约为5皮秒,通过沿轴朝着中心对称的1*相方向的层位移实现。层的剪切位移随泵浦通量增加,直到在约8皮米处达到饱和。我们证明,当使用光泵浦时,剪切声子的激发和亚稳相的稳定是解耦的,这一点在具有固定剪切声子的样品中观察到的转变也得到了证明。将结果与动态第一性原理模拟进行了比较,并根据一种机制对该转变进行了解释,即在亚稳相的原子位置稳定之前,瞬态局部无序很突出。漫散射结果证实了这一解释。层内振动激发与层间相互作用之间的相关性表明,在准确描述如何利用光场来操纵二维过渡金属二硫属化物的堆叠顺序时,纳入短程和长程相互作用都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c67/8291768/23ab347b3db6/nn1c01301_0001.jpg

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