Material and device design for organic optoelectronics
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Date
30/11/2011Author
Supervisor
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Abstract
This 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.
Type
Thesis, PhD Doctor of Philosophy
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