论文标题

2D-MOS2具有最狭窄的激子线宽,该线路通过无流量的直接加热而生长

2D-MoS2 with Narrowest Excitonic Linewidths Grown by Flow-Less Direct Heating of Bulk Powders

论文作者

Hejazi, Davoud, Tan, Renda, Rezapour, Neda Kari, Mojtabavi, Mehrnaz, Wanunu, Meni, Kar, Swastik

论文摘要

开发用于高质量合成单声道和较少复杂性和成本降低的2D材料的技术仍然是一个重要目标,既可以加速基础研究和应用开发。我们提出了最简单的可疑技术,可以合成MOS2的微米尺度单晶三角形单层,即通过将散装MOS2粉末直接加热到近端放置的底物上。与大多数在文献中报道的大多数其他技术获得的2D-MOS2相比,我们的样品的室温激发线宽值更窄,更均匀,并且与Ultraflat H-BN机械剥落的样品相当,表明其高质量。大多数其他技术生长或获得的样品中不存在丰富的特征拉曼光谱,也证明了我们样品的高质量。接触生长模式有助于晶体学圆形样品的直接生长,这使我们能够直接比较来自相同生长运行的扁平与紧张生长的光电特性。我们的方法首次允许定量比较菌株对激子和拉曼峰位置对相同合成的2D-MOS2的影响。应变在A-Exciton位置导致〜30 MeV的平均红移,在这些样品中的E12G拉曼峰中〜2 cm-1。我们的发现开辟了一些扩大2D物质研究的新可能性。通过消除对载气流,机械运动或化学反应的需求,我们的方法可以小型化,以实现低成本,高质量的科学研究或潜在地缩放,以便用于商业用途的2D晶体。此外,我们认为该技术也可以扩展到其他过渡金属二分法源和其他分层材料。

Developing techniques for high-quality synthesis of mono and few-layered 2D materials with lowered complexity and cost continues to remain an important goal, both for accelerating fundamental research and for applications development. We present the simplest conceivable technique to synthesize micrometer-scale single-crystal triangular monolayers of MoS2, i.e. by direct heating of bulk MoS2 powder onto proximally-placed substrates. Room-temperature excitonic linewidth values of our samples are narrower and more uniform than those of 2D-MoS2 obtained by most other techniques reported in literature, and comparable to those of ultraflat h-BN-capped mechanically exfoliated samples, indicative of their high quality. Feature-rich Raman spectra absent in samples grown or obtained by most other techniques, also stand out as a testament of the high quality of our samples. A contact-growth mode facilitates direct growth of crystallographically-strained circular samples, which allows us to directly compare the optoelectronic properties of flat vs. strained growth from the same growth runs. Our method allows, for the first time, to quantitatively compare the impact of strain on excitonic and Raman peak positions on identically-synthesized 2D-MoS2. Strain leads to average Red-shifts of ~ 30 meV in the A-exciton position, and ~ 2 cm-1 in the E12g Raman peak in these samples. Our findings open-up several new possibilities that expand 2D material research. By eliminating the need for carrier gas flow, mechanical motion or chemical reactions, our method can be either miniaturized for substantially low-cost, high-quality scientific research or potentially scaled-up for mass-production of 2D crystals for commercial purposes. Moreover, we believe this technique can also be extended to other transition metal dichalcogenides and other layered materials.

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