Raman spectroscopy of phonon states in NbTe4 and TaTe4 quasi-one-dimensional van der Waals crystals

IF 2.4 3区 化学 Q2 SPECTROSCOPY Journal of Raman Spectroscopy Pub Date : 2024-02-23 DOI:10.1002/jrs.6661
Zahra Ebrahim Nataj, Fariborz Kargar, Sergiy Krylyuk, Topojit Debnath, Maedeh Taheri, Subhajit Ghosh, Huairuo Zhang, Albert V. Davydov, Roger K. Lake, Alexander A. Balandin
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Abstract

We report the results of polarization-dependent Raman spectroscopy of phonon states in single-crystalline quasi-one-dimensional NbTe4 and TaTe4 van der Waals materials. The measurements were conducted in the wide temperature range from 80 to 560 K. Our results show that although both materials have identical crystal structures and symmetries, there is a drastic difference in the intensity of their Raman spectra. While TaTe4 exhibits well-defined peaks through the examined wavenumber and temperature ranges, NbTe4 reveals extremely weak Raman signatures. The measured spectral positions of the phonon peaks agree with the phonon band structure calculated using the density-functional theory. We offer possible reasons for the intensity differences between the two van der Waals materials. Our results provide insights into the phonon properties of NbTe4 and TaTe4 van der Waals materials and indicate the potential of Raman spectroscopy for studying charge-density-wave quantum condensate phases.

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NbTe4 和 TaTe4 准一维范德华晶体中声子态的拉曼光谱分析
我们报告了对单晶准一维 NbTe4 和 TaTe4 范德瓦耳斯材料中的声子态进行偏振相关拉曼光谱分析的结果。测量是在 80 至 560 K 的宽温度范围内进行的。我们的结果表明,尽管这两种材料的晶体结构和对称性完全相同,但它们的拉曼光谱强度却存在巨大差异。TaTe4 在所研究的波数和温度范围内都显示出清晰的峰值,而 NbTe4 则显示出极其微弱的拉曼光谱特征。测量到的声子峰光谱位置与使用密度泛函理论计算出的声子带结构一致。我们提出了两种范德华材料强度差异的可能原因。我们的研究结果提供了对 NbTe4 和 TaTe4 范德瓦耳斯材料声子特性的见解,并表明拉曼光谱在研究电荷密度波量子凝聚相方面的潜力。
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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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