2014
DOI: 10.1016/j.apsusc.2014.06.054
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Surface studies on benzophenone doped PDMS microstructures fabricated using KrF excimer laser direct write lithography

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Cited by 25 publications
(5 citation statements)
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“…In addition, the symmetric rocking, symmetric bending, asymmetric bending, symmetric stretching, and asymmetric stretching vibration modes of CH 3 appeared at 862, 1262, 1412, 2906, and 2965 cm -1 , respectively. This Raman spectrum of the EB-crosslinked PDMS was very consistent with the spectra in literatures [20][21][22]. In cases of the EB-irradiated composite films, typical Raman bands of both MWCNT and PDMS were detected, although the band intensities of MWCNT in the composite films were much higher than the ones of the PDMS matrix, owing to the strong Raman scattering capability of MWCNT in symmetric vibrational modes.…”
Section: Structural Characterizationsupporting
confidence: 86%
“…In addition, the symmetric rocking, symmetric bending, asymmetric bending, symmetric stretching, and asymmetric stretching vibration modes of CH 3 appeared at 862, 1262, 1412, 2906, and 2965 cm -1 , respectively. This Raman spectrum of the EB-crosslinked PDMS was very consistent with the spectra in literatures [20][21][22]. In cases of the EB-irradiated composite films, typical Raman bands of both MWCNT and PDMS were detected, although the band intensities of MWCNT in the composite films were much higher than the ones of the PDMS matrix, owing to the strong Raman scattering capability of MWCNT in symmetric vibrational modes.…”
Section: Structural Characterizationsupporting
confidence: 86%
“…50 Due to a large portion of fluorine in PVDF-HFP, XPS spectra of E-PH showed a quite-strong F 1s peak and a small C 1s peak. In the cases of E-M3 and E-M5 that were coated by the mixture of PVDF and PDMS, a relatively intensive O 1s peak was evidence of the Si−O−Si bond compared with E-PH, 51 and a new Si 2p peak that could be deconvoluted into the two components of Si−C and Si−O was exhibited; 52 however, in spite of the addition of PVDF, an F 1s peak did not appear. Considering the XPS focus on the surface chemical-composition analysis, this result was in line with the depiction of the microsphere-formation mechanism that is associated with the migration of PDMS molecules.…”
Section: Methodsmentioning
confidence: 97%
“…The Raman spectra of untreated wood, pure PDMS, and PDMS@wood samples are shown in Figure 4 . A typical Raman spectrum of the pure PDMS elastomer material showed the following peaks characterizing the various chemical bonds in the polymer; 490 cm −1 (Si-O-Si symmetric stretching), 712 cm −1 (Si-C symmetric stretching), 787 cm −1 (CH 3 asymmetric rocking and Si-C asymmetric stretching), 859 cm −1 (CH 3 symmetric rocking), 1262 cm −1 (CH 3 symmetric bending), 1411 cm −1 (CH 3 asymmetric bending), 2908 cm −1 (CH 3 symmetric stretching), and 2908 cm −1 (CH 3 asymmetric stretching) [ 30 , 31 , 32 ]. The pronounced peaks originating from Si-O-Si symmetric stretching at 490 cm −1 , Si-C symmetric stretching at 712 cm −1 , and CH 3 asymmetric stretching at 2970 cm −1 observed on the PDMS@wood surface were attributed to the successful adhesion of the PDMS to the wood surface.…”
Section: Resultsmentioning
confidence: 99%