Revealing anisotropic strain in exfoliated graphene by polarized Raman spectroscopy
We report on a polarized Raman study on mechanically cleaved single-layer graphene films. Under a specific orientation of scattering measurement, the width and position of the G peak change with the incident polarization direction, while the integrated intensity of that is unaltered. This phenomenon...
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Published in | Nanoscale Vol. 5; no. 20; pp. 9626 - 9632 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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21.10.2013
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Abstract | We report on a polarized Raman study on mechanically cleaved single-layer graphene films. Under a specific orientation of scattering measurement, the width and position of the G peak change with the incident polarization direction, while the integrated intensity of that is unaltered. This phenomenon is explained by a proposed mode in which the peak is contributed by a mixture of un-, compressive-, and tensile-strained G sub-modes. The compression and tension are both uniaxial and approximately perpendicular to each other. They are undesigned and located in either separated or overlapped sub-areas within the probed local region. Compared to the unstrained wavenumber of 1580 cm(-1), compression induces a blue shift while tension causes a red one. The sub-modes correlated with the light polarization through different relationships split the G peak into three sub-ones. We develop a method to quantitatively analyze the positions, widths, intensities, and polarization dependences of sub-peaks. This analysis quantitatively reveals local strain, which changes with the detected area of a graphene film. The method presented here can be extended to detect the strain distribution in the film and thus is a promising technology for graphene characterization. |
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AbstractList | We report on a polarized Raman study on mechanically cleaved single-layer graphene films. Under a specific orientation of scattering measurement, the width and position of the G peak change with the incident polarization direction, while the integrated intensity of that is unaltered. This phenomenon is explained by a proposed mode in which the peak is contributed by a mixture of un-, compressive-, and tensile-strained G sub-modes. The compression and tension are both uniaxial and approximately perpendicular to each other. They are undesigned and located in either separated or overlapped sub-areas within the probed local region. Compared to the unstrained wavenumber of 1580 cm(-1), compression induces a blue shift while tension causes a red one. The sub-modes correlated with the light polarization through different relationships split the G peak into three sub-ones. We develop a method to quantitatively analyze the positions, widths, intensities, and polarization dependences of sub-peaks. This analysis quantitatively reveals local strain, which changes with the detected area of a graphene film. The method presented here can be extended to detect the strain distribution in the film and thus is a promising technology for graphene characterization. We report on a polarized Raman study on mechanically cleaved single-layer graphene films. Under a specific orientation of scattering measurement, the width and position of the G peak change with the incident polarization direction, while the integrated intensity of that is unaltered. This phenomenon is explained by a proposed mode in which the peak is contributed by a mixture of un-, compressive-, and tensile-strained G sub-modes. The compression and tension are both uniaxial and approximately perpendicular to each other. They are undesigned and located in either separated or overlapped sub-areas within the probed local region. Compared to the unstrained wavenumber of 1580 cm super(-1), compression induces a blue shift while tension causes a red one. The sub-modes correlated with the light polarization through different relationships split the G peak into three sub-ones. We develop a method to quantitatively analyze the positions, widths, intensities, and polarization dependences of sub-peaks. This analysis quantitatively reveals local strain, which changes with the detected area of a graphene film. The method presented here can be extended to detect the strain distribution in the film and thus is a promising technology for graphene characterization. |
Author | Huang, Cheng-Wen Wang, Juen-Kai Liu, Chih-Yi Tzeng, Yonhua Chui, Hsiang-Chen Wang, Wei-Hua Shiue, Ren-Jye |
Author_xml | – sequence: 1 givenname: Cheng-Wen surname: Huang fullname: Huang, Cheng-Wen email: chihiliu@mail.ncku.edu.tw organization: Department of Photonics, National Cheng Kung University, Tainan 70101, Taiwan. chihiliu@mail.ncku.edu.tw – sequence: 2 givenname: Ren-Jye surname: Shiue fullname: Shiue, Ren-Jye – sequence: 3 givenname: Hsiang-Chen surname: Chui fullname: Chui, Hsiang-Chen – sequence: 4 givenname: Wei-Hua surname: Wang fullname: Wang, Wei-Hua – sequence: 5 givenname: Juen-Kai surname: Wang fullname: Wang, Juen-Kai – sequence: 6 givenname: Yonhua surname: Tzeng fullname: Tzeng, Yonhua – sequence: 7 givenname: Chih-Yi surname: Liu fullname: Liu, Chih-Yi |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23852110$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Anisotropy Blue shift Graphene Nanostructure Polarization Strain Strain distribution Wavenumber |
Title | Revealing anisotropic strain in exfoliated graphene by polarized Raman spectroscopy |
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