Please use this identifier to cite or link to this item:
|Title:||Raman spectroscopy of phenylcarbyne polymer films under pulsed green laser irradiation|
|Authors:||Lu, Y.F. |
|Source:||Lu, Y.F.,Huang, S.M.,Sun, Z. (2000-01-15). Raman spectroscopy of phenylcarbyne polymer films under pulsed green laser irradiation. Journal of Applied Physics 87 (2) : 945-951. ScholarBank@NUS Repository.|
|Abstract:||The polycarbyne polymer films were coated on silicon substrates and then irradiated by a pulsed Nd:yttrium-aluminum-garnet laser (λ=532 nm) with various fluences in argon gas atmosphere. Significant changes in microstructures and chemical bonding (sp3/sp2) during laser treatment were investigated by Raman spectroscopy. At a laser fluence below 50 mJ/cm2, the Raman spectrum of the film was similar to that of the original polymer film. In a fluence range from 100 to 650 mJ/cm2, the thermal decomposition of the polymer occurred, resulting in upshift of G peak and downshift of the D peak both with narrower peak width. With increasing laser fluence from 650 to 950 mJ/cm2, both the G and D peaks downshifted simultaneously due to the thermal decomposition. The simultaneous downshift of both peaks indicated the increased sp3/sp2 ratio in the carbon film converted from the polymer. With increasing laser fluence in this range, the thermal decomposition also induced the narrowing of both peaks. The narrowing of both peaks indicated the increased ordering of sp3 and sp2 bonding components in the converted carbon film. The scanning electron microscopy studies provided the further evidence. The carbon films converted from the polymer films may contain the highest sp3 carbon bonding at laser fluences in the range from 850 to 1000 mJ/cm2. © 2000 American Institute of Physics.|
|Source Title:||Journal of Applied Physics|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 17, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.