2006
DOI: 10.1016/j.vibspec.2005.06.005
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Surface-enhanced Raman scattering (SERS) of phthalic acid and 4-methyl phthalic acid on silver colloids as a function of pH

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Cited by 24 publications
(15 citation statements)
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“…4(A). Although there is some evidence to show the SERS peaks of PA are shifted under different pH and concentrations, [23] the reason for the wavenumber shift for different concentration here, we believe, is the difference in types of adsorption. Since the PA molecule is adsorbed on the surface of silver substrate after the droplet is dry, the pH value does not make sense in this case.…”
Section: Discussion and Future Outlookmentioning
confidence: 61%
“…4(A). Although there is some evidence to show the SERS peaks of PA are shifted under different pH and concentrations, [23] the reason for the wavenumber shift for different concentration here, we believe, is the difference in types of adsorption. Since the PA molecule is adsorbed on the surface of silver substrate after the droplet is dry, the pH value does not make sense in this case.…”
Section: Discussion and Future Outlookmentioning
confidence: 61%
“…For a typical Raman image with a scan range of 15 μm×15 μm, complete Raman spectra were acquired on every pixel with an integration time of 0.3 s per spectrum and an image resolution of 100 pixels×100 lines. To provide a careful analysis of the enhanced Raman scattering signal of phthalic acid on the sample features, all images presented here were processed by integrating the intensity of the Raman spectra at 1346 cm −1 (Supporting Information, Figure S1), which is attributed to the ν s (COO − ) mode of the carboxylate group 35. The microscopic length of the nanowire allows one to spectroscopically address and distinguish each set of nanostructures decorating the silica layer backing along the long wire axis independently.…”
Section: Methodsmentioning
confidence: 99%
“…27,28 The vibrational modes that are identified are listed on Table I and are assigned based on previous SERS work of -phenylalkanoic acids, carboxylic acids, and characteristic Raman frequencies of benzene derivatives. 27,28,[31][32][33][34][35][36] All samples show common peaks around 620, 1000, 1027, and 1600 cm −1 . These are believed to be modes associated with the phenyl ring of 6b, 12, 18, and 8a, respectively.…”
Section: Methodsmentioning
confidence: 99%