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

IF 2.4 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
{"title":"Resonance Raman Scattering of Topological Insulators Bi2Te3 and Bi2 − xSbxTe3 − ySey Thin Films","authors":"N. Kumar,&nbsp;N. V. Surovtsev,&nbsp;D. V. Ishchenko,&nbsp;P. A. Yunin,&nbsp;I. A. Milekhin,&nbsp;O. E. Tereshchenko,&nbsp;A. G. Milekhin","doi":"10.1002/jrs.6751","DOIUrl":null,"url":null,"abstract":"<p>Phonon occupation is temperature (<i>T</i>) dependent; it may participate in scattering with electronic states of topological insulators (TIs). 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. The study indicated that at high <i>T</i>, \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> mode and anharmonic coupling may become primary cause for scattering with electronic states of the TIs. However, at low <i>T</i>, primarily, both the LO phonons participated in the scattering.</p>","PeriodicalId":16926,"journal":{"name":"Journal of Raman Spectroscopy","volume":"56 3","pages":"207-217"},"PeriodicalIF":2.4000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Raman Spectroscopy","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jrs.6751","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
引用次数: 0

Abstract

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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