Department Lecture Series
Thursday November 1, 9:45
am, Smith 331
Small
Molecule Design for Organic Electronics
ABSTRACT: To fulfill the promise of low-cost large-area electronics
(displays, solar cells and solid-state lighting), materials
for organic electronic applications must be easily prepared,
stable, and amenable to solution deposition methods. The
latter requirement typically thwarts most efforts to develop
new materials - approaches to solubilize large aromatic chromophores
typically do so by disrupting the strong intermolecular interactions
necessary for electronic device performance. Our group has
taken a holistic approach to improving both solubility and
stability while simultaneously engineering the solid-state
organization of linear aromatic compounds to induce strong π-stacking
interactions. Separating the "waxy" solubilizing
substituent from the rigid aromatic core by a flexible alkyne
spacer allows the aromatic moieties to interact strongly,
while the solubilizing substituents segregate into domains
of insulating hydrocarbon. The ethyne substituent also increases
the oxidation potential of the aromatic chromophore, significantly
enhancing material stability. This approach to chromophore
functionalization has yielded high-performance materials
for thin film transistors, light emitting diodes and flexible
solar cells. Furthermore, the stabilization afforded by properly
selected substituents has allowed us to explore heretofore
poorly studied materials such as hexacene and heptacene.
This talk will focus on materials optimization for a variety
of electronic applications, and the relationship between
functionalization, crystal packing, thin-film morphology
and electronic device performance.
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