Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/6021
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dc.contributorDepartment of Industrial and Systems Engineering-
dc.creatorZeng, DW-
dc.creatorYung, KCW-
dc.creatorXie, CS-
dc.date.accessioned2014-12-11T08:24:59Z-
dc.date.available2014-12-11T08:24:59Z-
dc.identifier.issn0884-2914-
dc.identifier.urihttp://hdl.handle.net/10397/6021-
dc.language.isoenen_US
dc.publisherCambridge University Pressen_US
dc.rights© 2003 Materials Research Societyen_US
dc.rightsThe following article "D. W. Zeng, K. C. Yung and C. S. Xie (2003). Near-threshold ultraviolet-laser ablation of Kapton film investigated by x-ray photoelectron spectroscopy. Journal of Materials Research, 18(1), p. 53-59. doi:10.1557/JMR.2003.0008." is available at http://journals.cambridge.org/action/displayAbstract?fromPage=online&aid=7991176en_US
dc.subjectChemical bondsen_US
dc.subjectCompositionen_US
dc.subjectEthersen_US
dc.subjectLaser ablationen_US
dc.subjectOxidationen_US
dc.subjectPhotolysisen_US
dc.subjectX ray photoelectron spectroscopyen_US
dc.titleNear-threshold ultraviolet-laser ablation of Kapton film investigated by x-ray photoelectron spectroscopyen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationAuthor name used in this publication: K. C. Yungen_US
dc.identifier.spage53-
dc.identifier.epage59-
dc.identifier.volume18-
dc.identifier.issue1-
dc.identifier.doi10.1557/JMR.2003.0008-
dcterms.abstractNear-threshold ultraviolet-laser (355 nm) ablation of 125-μm thick Kapton films was investigated in detail using x-ray photoelectron spectroscopy. Different from the irradiation at higher fluences, the contents of the oxygen, amide group, and C-O group on the ablated surface increased with an increase in the pulse number, whereas the carbon contents decreased, although the contents of the nitrogen and the carbonyl group (C = O) decreased slightly. This implied that there was no carbon-rich residue on the ablated surface. Near the ablation threshold, only photolysis of the C-N bond in the imide rings and the diaryl ether group (C-O) took place due to a low surface temperature rise, and the amide structure and many unstable free radical groups were created. Sequentially, the oxidation reaction occurred to stabilize the free radical groups. The decomposition and oxidation mechanism could explain the intriguing changes of the chemical composition and characteristics of the ablated surface. In addition, the content of the C-O group depended on the opposite factors: the thermally induced decomposition of the ether groups and the pyrolysis of the C [aryl-C] bond. Upon further irradiation, the cumulative heating may induce the breakage of the C [sub aryl]-C bond and enhance the oxidation reaction, resulting in an increase of the content of the C-O group.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of materials research, Jan. 2003, v. 18, no. 1, p. 53-59-
dcterms.isPartOfJournal of materials research-
dcterms.issued2003-01-
dc.identifier.isiWOS:000180363400008-
dc.identifier.scopus2-s2.0-0037669663-
dc.identifier.eissn2044-5326-
dc.identifier.rosgroupidr13613-
dc.description.ros2002-2003 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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