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dc.contributor.advisorSamuel, Ifor D. W.
dc.contributor.authorLevell, Jack William
dc.coverage.spatial193en_US
dc.date.accessioned2011-11-24T12:37:38Z
dc.date.available2011-11-24T12:37:38Z
dc.date.issued2011-11-30
dc.identifier.urihttps://hdl.handle.net/10023/2066
dc.description.abstractThis thesis describes investigations into the photophysical properties of luminescent materials and their application in optoelectronic devices such as light emitting diodes and photodetectors. The materials used were all solution processable because of the interest in low cost processing of organics. I have investigated the photophysics of 1,4,5,8,9,12-hexamethyltriphenylene, a triphenylene derivative which has its luminescence enhanced by the addition of methyl groups. These groups change the planar shape of the triphenylene molecule into a twisted one, changing the symmetry of the molecule and increasing its dipole moment in absorption and emission by ~4 fold. This increased its rate of radiative deexcitation by ~20 times. In addition, the twisted shape of the molecule prevents intermolecular interactions and concentration effects from affecting the luminescence. This results in an efficient solid-state photoluminescence quantum yield of 31%. This thesis also includes an investigation into phosphorescent polymer dendrimers, designed to have suitable viscosities in solution for inkjet printed OLED applications. A photophysical study of the intra-chain aggregation effects on the luminescence was undertaken in both homopolymers and copolymers with high energy gap spacer units. Using double dendrons to increase the steric protection of the luminescent cores, the best homopolymers achieved 12.1% external quantum efficiency (39.3 cd/A) at 100 cd/m² brightness and the best co-polymer achieved 14.7% EQE (48.3 cd/A) at 100 cd/m². This compares favourably with 11.8% EQE for the best phosphorescent polymer and 16% for the best solution processed dendrimer OLED previously reported. Finally I have applied a solution processed enhancement layer to silicon photodiodes to enhance their ultraviolet response. Using a blend of materials to give favourable absorption and emission properties, 61% external quantum efficiency was achieved at 200 nm, which is better than the 20-30% typical for vacuum deposited lumogen enhancement layers used commercially.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.rightsCreative Commons Attribution-NoDerivs 3.0 Unported
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/
dc.subjectPhotophysicsen_US
dc.subjectIridium complexen_US
dc.subjectPolymeren_US
dc.subjectPhotodiodeen_US
dc.subjectLuminescenceen_US
dc.subjectPhosphorescenten_US
dc.subjectOLEDen_US
dc.subject.lccTK8304.L4en_US
dc.subject.lcshOptoelectronic devices--Design and constructionen_US
dc.subject.lcshOrganic compounds--Optical propertiesen_US
dc.subject.lcshOptical materialsen_US
dc.subject.lcshPhotodiodesen_US
dc.titleMaterial and device design for organic optoelectronicsen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


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