拓扑绝缘体Bi2Te3和Bi2 - xSbxTe3 - ySey薄膜的共振拉曼散射

IF 1.9 3区 化学 Q2 SPECTROSCOPY
N. Kumar, N. V. Surovtsev, D. V. Ishchenko, P. A. Yunin, I. A. Milekhin, O. E. Tereshchenko, A. G. Milekhin
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Longitudinal optical (LO) phonons \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>1</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;1 $$</annotation>\n </semantics></math> and \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>2</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;2 $$</annotation>\n </semantics></math> in Bi<sub>2 − x</sub>Sb<sub>x</sub>Te<sub>3 − y</sub>Se<sub>y</sub> (BSTS) was resonantly excited by a photon energy (E<sub><i>p</i></sub>) 2.33 eV due to electronic transition of unoccupied conduction band. The intensity of these modes was enhanced in Bi<sub>2</sub>Te<sub>3</sub> film at E<sub><i>p</i></sub> 1.87 eV, which is close to the electronic transition of unoccupied Dirac states. Fröhlich coupling strength was the main mechanism for higher intensity of \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>1</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;1 $$</annotation>\n </semantics></math> and \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>2</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;2 $$</annotation>\n </semantics></math> modes. At 300 K, the intensity of the \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>2</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;2 $$</annotation>\n </semantics></math> mode was significantly decayed in both the BSTS and Bi<sub>2</sub>Te<sub>3</sub> at E<sub><i>p</i></sub> 2.33 and 1.87 eV due to the anharmonic coupling. However, at similar value of <i>T</i>, spectral profile of \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>A</mi>\n <mrow>\n <mn>1</mn>\n <mi>g</mi>\n </mrow>\n <mn>1</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{A}}_{1g}&amp;#x0005E;1 $$</annotation>\n </semantics></math> and \n<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>E</mi>\n <mi>g</mi>\n <mn>2</mn>\n </msubsup>\n </mrow>\n <annotation>$$ {\\mathrm{E}}_g&amp;#x0005E;2 $$</annotation>\n </semantics></math> modes was not affected because of the lower probability of decay rate of these phonons. In resonant condition, well-resolved Raman forbidden surface modes were observed at <i>T</i> of 50 K. At 300 K, more asymmetric Fano profile of surface phonon was observed due to the anharmonic coupling. 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Longitudinal optical (LO) phonons \\n<span></span><math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>A</mi>\\n <mrow>\\n <mn>1</mn>\\n <mi>g</mi>\\n </mrow>\\n <mn>1</mn>\\n </msubsup>\\n </mrow>\\n <annotation>$$ {\\\\mathrm{A}}_{1g}&amp;#x0005E;1 $$</annotation>\\n </semantics></math> and \\n<span></span><math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>A</mi>\\n <mrow>\\n <mn>1</mn>\\n <mi>g</mi>\\n </mrow>\\n <mn>2</mn>\\n </msubsup>\\n </mrow>\\n <annotation>$$ {\\\\mathrm{A}}_{1g}&amp;#x0005E;2 $$</annotation>\\n </semantics></math> in Bi<sub>2 − x</sub>Sb<sub>x</sub>Te<sub>3 − y</sub>Se<sub>y</sub> (BSTS) was resonantly excited by a photon energy (E<sub><i>p</i></sub>) 2.33 eV due to electronic transition of unoccupied conduction band. The intensity of these modes was enhanced in Bi<sub>2</sub>Te<sub>3</sub> film at E<sub><i>p</i></sub> 1.87 eV, which is close to the electronic transition of unoccupied Dirac states. 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引用次数: 0

摘要

声子占用与温度(T)有关;它可能参与拓扑绝缘体的电子态散射。纵向光学(LO)声子a1g1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$和a1g2在Bi2−xSbxTe3−ySey (BSTS)中$$ {\mathrm{A}}_{1g}&#x0005E;2 $$,由于未占据的导带电子跃迁,光子能量(Ep)为2.33 eV而被共振激发。在Ep为1.87 eV时,这些模式的强度在Bi2Te3薄膜中得到增强,接近于无占据狄拉克态的电子跃迁。Fröhlich耦合强度是提高a1g强度的主要机制$$ {\mathrm{A}}_{1g}&#x0005E;1 $$和a1g2种$$ {\mathrm{A}}_{1g}&#x0005E;2 $$模式。在300 K时,由于非谐波耦合,BSTS和Bi2Te3在Ep为2.33和1.87 eV时的a1 g 2 $$ {\mathrm{A}}_{1g}&#x0005E;2 $$模式强度显著衰减。然而,在相似的T值下,a1g1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$和e2 $$ {\mathrm{E}}_g&#x0005E;2 $$模态的谱线不受影响因为这些声子的衰变率概率较低。在共振条件下,在温度为50 K时观察到分辨率较高的拉曼禁表面模式。在300 K时,由于非谐波耦合,表面声子的Fano分布更加不对称。研究表明,在高温度下,a1g1$$ {\mathrm{A}}_{1g}&#x0005E;1 $$模式和非谐波耦合可能成为ti与电子态散射的主要原因。然而,在低温度下,两个声子都参与了散射。
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 Scattering of Topological Insulators Bi2Te3 and Bi2 − xSbxTe3 − ySey Thin Films

Resonance Raman Scattering of Topological Insulators Bi2Te3 and Bi2 − xSbxTe3 − ySey Thin Films

Phonon occupation is temperature (T) dependent; it may participate in scattering with electronic states of topological insulators (TIs). Longitudinal optical (LO) phonons A 1 g 1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$ and A 1 g 2 $$ {\mathrm{A}}_{1g}&#x0005E;2 $$ in Bi2 − xSbxTe3 − ySey (BSTS) was resonantly excited by a photon energy (Ep) 2.33 eV due to electronic transition of unoccupied conduction band. The intensity of these modes was enhanced in Bi2Te3 film at Ep 1.87 eV, which is close to the electronic transition of unoccupied Dirac states. Fröhlich coupling strength was the main mechanism for higher intensity of A 1 g 1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$ and A 1 g 2 $$ {\mathrm{A}}_{1g}&#x0005E;2 $$ modes. At 300 K, the intensity of the A 1 g 2 $$ {\mathrm{A}}_{1g}&#x0005E;2 $$ mode was significantly decayed in both the BSTS and Bi2Te3 at Ep 2.33 and 1.87 eV due to the anharmonic coupling. However, at similar value of T, spectral profile of A 1 g 1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$ and E g 2 $$ {\mathrm{E}}_g&#x0005E;2 $$ modes was not affected because of the lower probability of decay rate of these phonons. In resonant condition, well-resolved Raman forbidden surface modes were observed at T of 50 K. At 300 K, more asymmetric Fano profile of surface phonon was observed due to the anharmonic coupling. The study indicated that at high T, A 1 g 1 $$ {\mathrm{A}}_{1g}&#x0005E;1 $$ mode and anharmonic coupling may become primary cause for scattering with electronic states of the TIs. However, at low T, primarily, both the LO phonons participated in the scattering.

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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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