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Investigation of the Optoelectronic Properties of Organic Light-Emitting Transistors Based on an Intrinsically Ambipolar Material

Academic Article
Publication Date:
2008
abstract:
The realization of organic light-emitting transistors (OLETs) based on R,?-dihexylcarbonylquaterthiophene (DHCO4T), an intrinsically ambipolar and luminescent semiconductor, is reported. In this device structure, optimization of the hole/electron density ratio in the channel region has been identified as the major issue to optimize light emission.. Therefore, the focus of this study is to understand how DHCO4T optoelectronic response vary with semiconductor film growth conditions as well as the selection of the gate dielectric and metal contact materials. Our results demonstrate that DHCO4T hole and electron mobilities and the IDS-VDS hysteresis mainly depend on the gate dielectric material composition. Atomic force microscopy analysis of the semiconductor film reveals a layer-by-layer growth mechanism, giving rise to the formation of a continuous and homogeneous charge transport layers. With Au as the source and drain contact material, the best carrier mobilities have been measured for the poly(methyl methacrylate)-coated SiO2 gate dielectric devices. Metals with Fermi energy ranging from -5.1 to -2.87 eV have also been investigated. Metal deposition on the semiconductor film does not significantly affect film morphology as evidenced by the topography of the electrode top surface. However, for a given dielectric material, the OLET performance strongly depends on the metal/dielectric combination employed and marginally correlates with the contact Fermi energy. Electroluminescence has been observed in DHCO4T-based OLETs but principally in concert with unipolar transport. The hole and electron large gate threshold voltage values have been identified as the principal limitation to high electroluminescence performances.
Iris type:
01.01 Articolo in rivista
List of contributors:
Muccini, Michele; Murgia, Mauro; Capelli, Raffaella; Toffanin, Stefano
Authors of the University:
MUCCINI MICHELE
MURGIA MAURO
TOFFANIN STEFANO
Handle:
https://iris.cnr.it/handle/20.500.14243/231925
Published in:
JOURNAL OF PHYSICAL CHEMISTRY. C
Journal
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