ABSTRACT
The secondary kinetic isotope effects (KIEs) of red phosphorescent Ir(III) complexes and the corresponding devices have been investigated. The selective deuterated red emitters show negligible influence on the luminescent spectra, but have positive effects on the quantum efficiencies and stabilities in the devices. As secondary KIEs predicted, the photolysis coinciding with the electrolysis of the deuterated complexes in the devices, measured via decreasing of luminescent intensity, are reduced in rate. An about 33% increase of the device working lifetime could be readily obtained with the strategy of selective deuteration on the emitter complexes. The findings demonstrate the importance of the isotopic effect on the performance improvement of organic light emitting devices and will also trigger the study on organic optoelectronic materials via isotopic tools.
ABSTRACT
Poly(3,4ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) has been intensively studied for its thermoelectric applications. Structural modulation to improve crystalline ordering, chain conformation and film morphology is a promising way to decouple the trade-off between conductivity and Seebeck coefficient and thus improve the thermoelectric power factor. Post treatment with ionic liquid ([CoCl2 â 6H2 O]:[ChCl]) bearing cobalt-containing anions resulted in a remarkable enhancement of the power factor to 76.8â µW m-1 K-2 . This IL combines the influence of a high-boiling polar organic solvent and diffusing ions. A high σ mainly resulted from the efficient removal of PSS chains, ordering of the structure and delocalization of bipoloran-dominant transport after conformational change. The increase in S was not due to dedoping of PEDOT chains, but rather the sharp feature of the density of states at the Fermi level induced by ion-exchange with unconventional anions.
