Abstract
The charge transport properties of three tertiary-butyl (t-Bu) substituted anthracene derivatives (ADN), critical blue host materials for organic light-emitting diodes (OLEDs), have been investigated experimentally and computationally. From time-of-flight (TOF) measurements, all ADN compounds exhibit ambipolar characters. The hole and electron mobilities are in the range (1-5) × 10-7cm2V-1 s-1 under an external applied field of about 1MVcm-1. Un-substituted ADN has the highest carrier mobilities while heavily t-Bu substituted ADN has the least. The electron and hole conducting properties of are consistent with ab initio calculation, which indicates that the frontier orbitals are localized mainly on the anthracene moiety. t-Bu substitutions in ADN increase the hopping path lengths among the molecules and hence reduce the electron and hole mobilities. The results demonstrate that t-Bu substitution is an effective means of engineering the conductivity of organic charge transporter for OLED applications.
Original language | English |
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Pages (from-to) | 555-557 |
Number of pages | 3 |
Journal | Japanese Journal of Applied Physics |
Volume | 45 |
Issue number | 1 B |
DOIs | |
Publication status | Published - 20 Jan 2006 |
Scopus Subject Areas
- General Engineering
- General Physics and Astronomy
User-Defined Keywords
- Ambipolar
- Anthracene derivative
- Carrier mobility