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A Bipolar Host Material Containing Triphenylamine and Diphenylphosphoryl-Substituted Fluorene Units for Highly Efficient Blue Electrophosphorescence



Highly efficient blue electrophosphorescent organic light-emitting diodes incorporating a bipolar host, 2,7-bis(diphenylphosphoryl)-9-[4-(N,N-diphenylamino)phenyl]-9-phenylfluorene (POAPF), doped with a conventional blue triplet emitter, iridium(III) bis[(4,6-difluoro-phenyl)pyridinato-N,C]picolinate (FIrpic) are fabricated. The molecular architecture of POAPF features an electron-donating (p-type) triphenylamine group and an electron-accepting (n-type) 2,7-bis(diphenyl-phosphoryl)fluorene segment linked through the sp3-hybridized C9 position of the fluorene unit. The lack of conjugation between these p- and n-type groups endows POAPF with a triplet energy gap (ET) of 2.75 eV, which is sufficiently high to confine the triplet excitons on the blue-emitting guest. In addition, the built-in bipolar functionality facilitates both electron and hole injection. As a result, a POAPF-based device doped with 7 wt% FIrpic exhibits a very low turn-on voltage (2.5 V) and high electroluminescence efficiencies (20.6% and 36.7 lm W−1). Even at the practical brightnesses of 100 and 1000 cd m−2, the efficiencies remain high (20.2%/33.8 lm W−1 and 18.8%/24.3 lm W−1, respectively), making POAPF a promising material for use in low-power-consumption devices for next-generation flat-panel displays and light sources.

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