2008
DOI: 10.1088/1464-4258/10/5/055303
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Raman spectra of polymethyl methacrylate optical fibres excited by a 532 nm diode pumped solid state laser

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Cited by 150 publications
(89 citation statements)
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“…The energy difference between the excitation and the emission peak is calculated in the wave numbers using the relation ΔE/hc (cm -1 ) = 1/λext -1/λem, where λext and λem are excitation and emission wavelengths respectively. For PMMA, the emission peaks due to excitation wavelengths at 458, 488, 530, and 560 nm nearly match the Raman mode of characteristic peak at 1736 cm -1 of γ (C=O) of (C-COO) mode [47]. Excitations at 380, and 400 nm nearly match with Raman mode of 3454 cm -1 which is 2γ2 overtone of 1730 cm -1 .…”
Section: Methodsmentioning
confidence: 63%
“…The energy difference between the excitation and the emission peak is calculated in the wave numbers using the relation ΔE/hc (cm -1 ) = 1/λext -1/λem, where λext and λem are excitation and emission wavelengths respectively. For PMMA, the emission peaks due to excitation wavelengths at 458, 488, 530, and 560 nm nearly match the Raman mode of characteristic peak at 1736 cm -1 of γ (C=O) of (C-COO) mode [47]. Excitations at 380, and 400 nm nearly match with Raman mode of 3454 cm -1 which is 2γ2 overtone of 1730 cm -1 .…”
Section: Methodsmentioning
confidence: 63%
“…However, the presence of low-intensity D band (1355 cm -1 ), originating from disordered carbon atoms in A 0 1 symmetry [27], indicates the small number of structural defects introduced into the graphene sample. No bands corresponded to PMMA (the most intensive are 1460, 1736 and 2957 cm -1 ) [28] were observed in this Raman spectrum proving no contamination of the transferred graphene with polymer residues. Figure 3b, c show SEM images of bismuth selenide nanostructures, deposited on monolayer CVD graphene substrate as a result of two-stage synthesis.…”
Section: Methodsmentioning
confidence: 72%
“…These could only be partly corrected by the background, due to its specific nature discussed below. We connect the structure in the range 1730-1740 cm −1 to Perspex, the material of the holder of the chip, of which the spectrum shows a peak at 1736 cm −1 [22]. The residual structures at 1900 and 1960 cm −1 , clearly present in both the raw spectra and the background, so far remain unidentified, although we note that they occur in the range of Raman signatures of hydrocarbon chains.…”
Section: Raman Spectroscopymentioning
confidence: 93%