XPS investigation of Upilex-S polyimide ablated by 355 nm Nd : YAG laser irradiation

Citation
Kc. Yung et al., XPS investigation of Upilex-S polyimide ablated by 355 nm Nd : YAG laser irradiation, APPL SURF S, 173(3-4), 2001, pp. 193-202
Citations number
30
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
APPLIED SURFACE SCIENCE
ISSN journal
01694332 → ACNP
Volume
173
Issue
3-4
Year of publication
2001
Pages
193 - 202
Database
ISI
SICI code
0169-4332(20010329)173:3-4<193:XIOUPA>2.0.ZU;2-9
Abstract
Laser ablation of Upilex-S polyimide films 80 mum thick was performed using a 355 nm pulsed Nd:YAG laser. Nanoparticles redeposited at the ablated zon e and at the edge of the hole were observed. Chemical and structural change s of the Upilex-S polyimide surface after 355 nm laser irradiation in air w ere analyzed by X-ray photoelectron spectroscopy (XPS). Relative C content in the ablated zone was found to be higher, while both O and N contents wer e lower than in the untreated area. This indicates that laser irradiation r eleased O and N atoms, and that the nanoparticles formed in the ablated zon e consist mainly of carbon clusters. After deconvoluting the C 1s and O 1s spectra, three new components related to the carboxylate (O-C=O), ether (C- O), and dropC=O groups were detected in and around the ablated zone. In add ition, one new component was found for O Is spectra, and the peak at 288.2 eV related to the imide carbonyl groups was shifted by 0.2-0.6 eV. These ef fects are probably due to the oxidation and formation of a non-imide carbon yl group. At the edge of the hole enhanced oxidation was found: the C conte nt was considerably lower than that in the ablated zone, and the C 1s peak was at 288.6 +/- 0.2 eV. This suggests the formation of oxidized nano-parti cles, which carry the non-imide carbonyl groups. Based on these results, th e decomposition of Upilex-S polyimide irradiated by UV light occurs via a p hotothermal ablation process. (C) 2001 Elsevier Science B.V. All rights res erved.