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首页> 外文期刊>Science Advances >Tunable and laser-reconfigurable 2D heterocrystals obtained by epitaxial stacking of crystallographically incommensurate Bi2Se3 and MoS2 atomic layers
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Tunable and laser-reconfigurable 2D heterocrystals obtained by epitaxial stacking of crystallographically incommensurate Bi2Se3 and MoS2 atomic layers

机译:通过晶体学上不相称的Bi 2 Se 3 和MoS 2 原子层的外延堆叠获得可调谐和激光可重构的2D杂晶

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Vertical stacking is widely viewed as a promising approach for designing advanced functionalities using two-dimensional (2D) materials. Combining crystallographically commensurate materials in these 2D stacks has been shown to result in rich new electronic structure, magnetotransport, and optical properties. In this context, vertical stacks of crystallographically incommensurate 2D materials with well-defined crystallographic order are a counterintuitive concept and, hence, fundamentally intriguing. We show that crystallographically dissimilar and incommensurate atomically thin MoS2 and Bi2Se3 layers can form rotationally aligned stacks with long-range crystallographic order. Our first-principles theoretical modeling predicts heterocrystal electronic band structures, which are quite distinct from those of the parent crystals, characterized with an indirect bandgap. Experiments reveal striking optical changes when Bi2Se3 is stacked layer by layer on monolayer MoS2, including 100% photoluminescence (PL) suppression, tunable transmittance edge (1.1→0.75 eV), suppressed Raman, and wide-band evolution of spectral transmittance. Disrupting the interface using a focused laser results in a marked the reversal of PL, Raman, and transmittance, demonstrating for the first time that in situ manipulation of interfaces can enable “reconfigurable” 2D materials. We demonstrate submicrometer resolution, “laser-drawing” and “bit-writing,” and novel laser-induced broadband light emission in these heterocrystal sheets.
机译:垂直堆叠被广泛认为是使用二维(2D)材料设计高级功能的有前途的方法。在这些2D堆栈中组合晶体学上相称的材料已显示出丰富的新电子结构,磁传输和光学特性。在这种情况下,晶体学上不相称的2D材料的垂直堆栈具有明确的晶体学顺序是违反直觉的概念,因此从根本上讲是令人着迷的。我们表明,晶体学上不相似且不相称的原子薄的MoS 2 和Bi 2 Se 3 层可以形成具有长程晶体学顺序的旋转排列的叠层。我们的第一原理理论模型预测异晶电子能带结构,该结构与母体晶体的结构截然不同,其特征是间接带隙。实验揭示了Bi 2 Se 3 在单层MoS 2 上逐层堆叠时的惊人光学变化,包括100%光致发光(PL)抑制,可调的透射率边缘(1.1→0.75 eV),拉曼抑制和光谱透射率的宽带演化。使用聚焦激光破坏界面会导致PL,拉曼和透射率的显着逆转,这首次证明界面的原位操作可以启用“可重构” 2D材料。我们展示了亚微米分辨率,“激光绘图”和“位写入”,以及这些异晶片中新颖的激光诱导宽带发光。

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