Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/4209
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Applied Physics-
dc.creatorLu, SG-
dc.creatorXu, ZK-
dc.creatorChen, H-
dc.creatorMak, CL-
dc.creatorWong, KH-
dc.creatorLi, KF-
dc.creatorCheah, KW-
dc.date.accessioned2014-12-11T08:24:57Z-
dc.date.available2014-12-11T08:24:57Z-
dc.identifier.issn0021-8979-
dc.identifier.urihttp://hdl.handle.net/10397/4209-
dc.language.isoenen_US
dc.publisherAmerican Institute of Physicsen_US
dc.rights© 2006 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in S. G. Lu et al., J. Appl. Phys. 99, 064103 (2006) and may be found at http://link.aip.org/link/?jap/99/064103.en_US
dc.subjectBarium compoundsen_US
dc.subjectPowdersen_US
dc.subjectPhotoluminescenceen_US
dc.subjectSpectral line shiften_US
dc.subjectParticle sizeen_US
dc.subjectSurface statesen_US
dc.subjectValence bandsen_US
dc.subjectExcitonsen_US
dc.titleTime-resolved photoluminescence of barium titanate ultrafine powdersen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationAuthor name used in this publication: C. L. Maken_US
dc.description.otherinformationAuthor name used in this publication: K. H. Wongen_US
dc.identifier.spage1-
dc.identifier.epage4-
dc.identifier.volume99-
dc.identifier.issue6-
dc.identifier.doi10.1063/1.2182075-
dcterms.abstractTime-resolved photoluminescence (PL) near 540 nm, taken from barium titanate (BaTiO₃) ultrafine powders of ~80, 90, and 110 nm in size, was measured at 11 K. Two-exponential functions were found to fit the decay curves well, and the decay lifetimes were composed of one short, about 10 ns, and one long, about 200 ns, time constants, respectively. Results also indicate that the PL peaks show a small blueshift with decreasing BaTiO₃particle size. The decay process consists of the recombination of self-trapped excitons (long lifetime decay) and of the electrons in the surface states with the holes in the valence band (short lifetime decay). The short lifetime component makes comparable contribution to the decay intensity of PL with the long lifetime one.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of applied physics, 15 Mar. 2006, v. 99, no. 6, 064103, p. 1-4-
dcterms.isPartOfJournal of applied physics-
dcterms.issued2006-03-15-
dc.identifier.isiWOS:000236464400049-
dc.identifier.scopus2-s2.0-33645696839-
dc.identifier.eissn1089-7550-
dc.identifier.rosgroupidr29403-
dc.description.ros2005-2006 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
Lu_Time-resolved_photoluminescence.pdf182.33 kBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

169
Last Week
1
Last month
Citations as of Apr 14, 2024

Downloads

259
Citations as of Apr 14, 2024

SCOPUSTM   
Citations

49
Last Week
0
Last month
0
Citations as of Apr 19, 2024

WEB OF SCIENCETM
Citations

56
Last Week
0
Last month
0
Citations as of Apr 18, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.