Show simple item record

dc.contributor.authorAl-Imarah, Emad Mohamed Abdulrazaq
dc.date.accessioned2014-06-11T22:03:26Z
dc.date.available2014-06-11T22:03:26Z
dc.date.issued2014
dc.identifier.urihttp://hdl.handle.net/10179/5457
dc.description.abstractA designed series of novel boron-difluoride chelated aza-dipyrromethenes with particular physical properties have been synthesized for the purpose of exploring their usefulness as donors in organic photovoltaic (OPV) cells. Boron-difluoride chelated aza-dipyrromethenes are commonly referred in the literature as aza-BODIPYs, and this convention has been adopted in this thesis. The aza-BODIPYs synthesised were symmetrically substituted with aryl groups on the pyrrole rings. The synthesised aza-BODIPYs were: terthiophene-BF2- aza-dipyrromethene (87), methoxy-terthiophene-BF2-aza-dipyrromethene (88), triphenylamine-BF2-aza-dipyrromethene (100), thiophene-triphenylamine-BF2-azadipyrromethene (106), benzothiadiazole-BF2-aza-dipyrromethene (111), benzothiadiazole-thiophene-BF2-aza-dipyrromethene (112), benzothiadiazoletriphenylamine- BF2-aza-dipyrromethene (113), ethylenedioxythiophene-BF2-azadipyrromethene (125), thiophene-phenothiazine-BF2-aza-dipyrromethene (132), thiophene-methylpyrrole-BF2-aza-dipyrromethene (139), thiophene-carbazole-BF2-azadipyrromethene (145), fluorenone-BF2-aza-dipyrromethene (150), and thiophenefluorenone- BF2-aza-dipyrromethene (151). The numbers are used to refer to individual compounds in this thesis. Ruthenium dyes, terthiophene monomers and silicon quantum dots were also synthesised, again with a view to discovering novel donors for OPV cells. The aza-BODIPYs were characterized spectroscopically by ultraviolet-visible (UV-VIS) absorption spectroscopy, fluorescence and time-correlated single-photon counting (TCSPC). Benzothiadiazole-triphenylamine-BF2-aza-dipyrromethene (referred to as compound (113) in this thesis) was found to exhibit significant red-shifts in absorption (?max=855 nm) and emission (?em=953 nm). This compound showed a large bathochromic shift (205 nm) in absorption, in comparison with the standard BF2-tetra-aryl azadipyrromethene (compound (4), ?max=650 nm). Evidence has been found of strong intramolecular-charge-transfer (ICT) character in the excited state. It has been demonstrated how absorption and emission of aza-BODIPYs can be fine-tuned by manipulating the ICT between variously electronic donating and withdrawing substituents in the aza-BODIPY structure. Fluorescence and time-correlated single-photon counting (TCSPC) on the aza-BODIPYs in the presence of fullerenes supported the conclusion that there were charge transfer processes Time-dependent density functional theory (TD-DFT) has been successfully used to provide a guide to the structure-property relationships and electronic structures of the aza- BODIPYs. Absorption energies, calculated for the aza-BODIPYs using the B3LYP (Becke, three-parameter, Lee-Yang-Parr) exchange-correlation functional with a splitvalence basis set of 6-311++G (2d, P). The B3LYP/6-311++G (2d, P) level of calculation delivered reasonable estimates of the absorption wavelengths for a number of the aza-BODIPYs, although the calculations did give poor estimates for the absorption wavelengths of others. Photovoltaic devices were fabricated, using primarily carbon-60 fullerene as acceptor in conjunction with the aza-BODIPYs as donors, and successfully generated current on exposure to simulated solar radiation. Using a xenon arc lamp as a solar simulator, external photon-to-current quantum efficiencies (EQE) and overall power conversion efficiencies (?) were measured for these devices with a variety of layer structures, film compositions and film-processing conditions. Compound (106) and compound (113) gave EQEs of 3.89% and 3.01%, and overall power conversion efficiencies of 0.88% and 0.031% respectively. Current density-voltage (J-V) curves exhibit a significant inflection, which was reflected in the low fill factors (FF). The low values of EQE and ? are attributed to low open-circuit voltage (VOC) (0.32 V and 0.55 V in compounds (106) and (113)) and low fill factors (FF) (0.312 and 0.0147 in compounds (106) and (113)). The low VOC and FF are possibly the result of an interfacial extraction barrier at one of the active layer interfaces, possibly between the active layer and the metal cathode. Avoiding the possibility of oxide and other layers through encapsulating the devices in an inert environment might remove the charge extraction barrier. The conclusion drawn is efficiencies of devices based on aza-BODIPYs might be improved significantly through further studies of interfaces and defects in devices.en
dc.language.isoenen
dc.publisherMassey Universityen_US
dc.rightsThe Authoren_US
dc.subjectPhotovoltaic cellsen
dc.subjectPhotovoltaic power generationen
dc.subjectOrganic semiconductorsen
dc.titleSynthesis, characterization and evaluation of aza-dipyrromethenes and other small molecules for organic photovoltaics : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Chemistry, Massey University, Te Kunenga ki Pūrehuroa, University of New Zealand, Palmerston North, New Zealanden
dc.typeThesisen
thesis.degree.disciplineChemistryen
thesis.degree.grantorMassey Universityen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophy (Ph.D.)en


Files in this item

Icon
Icon

This item appears in the following Collection(s)

Show simple item record