关于声子软化、声子寿命、法诺共振和 MoS2 纳米片多峰值分析的共振拉曼研究

IF 2.4 3区 化学 Q2 SPECTROSCOPY
Susmitha Balagopalan, Balasubramanian Karthikeyan
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引用次数: 0

摘要

在这项研究中,我们研究了在 633 纳米激光的激发下,水热法生产的 2H-MoS2 纳米片的共振拉曼光谱。光谱观测结果包括基本的 MoS2 模式和附加拉曼线,后者是由于激光辐射入射导致半导体能态改变而产生的。我们计算了不同激光功率下的声子软化和声子寿命的变化。在不同激光功率下,分析了导致拉曼光谱线不对称的法诺共振。法诺线形函数用于拟合平面内振动模式的不对称,而使用法诺-洛伦兹函数的多峰拟合则用于拟合与 "b "模式耦合的平面外基本模式。利用 "b "模式对电子-声子相互作用进行了直接研究。然后利用在共振拉曼光谱中观察到的 2LA(M) 模式研究了激光波长的偏移。这些发现为新的光电设备设计者提供了对过渡金属二卤化物中错综复杂的电子-声子相互作用的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Resonance Raman studies on phonon softening, phonon lifetime, Fano resonance, and multipeak analysis of MoS2 nanoflakes

Resonance Raman studies on phonon softening, phonon lifetime, Fano resonance, and multipeak analysis of MoS2 nanoflakes

In this study, the resonance Raman spectra of hydrothermally produced 2H-MoS2 nanoflakes excited by a 633-nm laser were examined. Spectral observations include both fundamental MoS2 modes and additional Raman lines, which arise from alterations in the energy states of the semiconductor owing to the incidence of laser radiation. Phonon softening and alterations in the phonon lifetime were computed for different laser powers. The Fano resonance, which causes asymmetry in the Raman spectral lines, was analyzed at different laser powers. The Fano line-shape function is used to fit the asymmetry in the in-plane vibrational mode whereas multi-peak fitting using the Fano-Lorentzian function is used to fit the out-of-the-plane fundamental mode, which is coupled with “b” mode. A direct study of the electron–phonon interaction was carried out with the “b” mode. The shift in laser wavenumber was then investigated using the 2LA(M) modes observed in the resonance Raman spectra. These findings provide new optoelectronic device designers with an understanding of the intricate electron–phonon interactions in transition metal dichalcogenides.

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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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