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dc.contributor.authorD. Channeien_US
dc.contributor.authorA. Nakaruken_US
dc.contributor.authorS. Phanichphanten_US
dc.contributor.authorP. Koshyen_US
dc.contributor.authorC. C. Sorrellen_US
dc.date.accessioned2018-09-04T09:24:27Z-
dc.date.available2018-09-04T09:24:27Z-
dc.date.issued2013-08-05en_US
dc.identifier.issn20909071en_US
dc.identifier.issn20909063en_US
dc.identifier.other2-s2.0-84880856018en_US
dc.identifier.other10.1155/2013/579284en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880856018&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52385-
dc.description.abstractCerium dioxide (CeO2) thin films with varying Ce concentrations (0.1 to 0.9 M, metal basis) were deposited on soda-lime-silica glass substrates using spin coating. It was found that all films exhibited the cubic fluorite structure after annealing at 500°C for 5 h. The laser Raman microspectroscopy and GAXRD analyses revealed that increasing concentrations of Ce resulted in an increase in the degree of crystallinity. FIB and FESEM images confirmed the laser Raman and GAXRD analyses results owing to the predicted increase in film thickness with increasing Ce concentration. However, porosity and shrinkage (drying) cracking of the films also increased significantly with increasing Ce concentrations. UV-VIS spectrophotometry data showed that the transmission of the films decreased with increasing Ce concentrations due to the increasing crack formation. Furthermore, a red shift was observed with increasing Ce concentrations, which resulted in a decrease in the optical indirect band gap. © 2013 D. Channei et al.en_US
dc.subjectChemistryen_US
dc.titleCerium dioxide thin films using spin coatingen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Chemistryen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of New South Wales (UNSW) Australiaen_US
Appears in Collections:CMUL: Journal Articles

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