Answers are grounded in this paper and cite their sources.
A series of 2-(stilben-4-yl)benzoxazole derivatives (BOXSB-X) was prepared and used as a dopant in the fabrication of organic light-emitting diodes. With a device structure of ITO/NPB/CBP/TPBI:3%BOXSB-X/TPBI/Mg:Ag, where NPB, CBP, and TPBI stand for 4,4‘-bis[ N -(1-naphthyl)- N -phenyl-amino]-biphenyl, 4,4‘-dicarbazolyl-1,1‘-biphenyl, and 2,2‘,2‘ ‘-(1,3,5-phenylene)tris-[1-phenyl-1H-benzimidazole], respectively, light emission from the dopant was observed under electric bias, presumably due to energy transfer between the host TPBI exciton and the dopant. Bright blue emission with a luminance ranging between 8 000 and 13 000 cd/m 2 was obtained depending on the substituent on the stilbene moiety. However, with a device structure of ITO/NPB/TPBI:3%BOXSB-X/TPBI/Mg:Ag, where no CBP layer was present, the recombination/emission region shifted to the NPB layer except in the device doped with dimethylamino-substituted benzoxazole derivative, in which case the carrier trap mechanism is suggested to be responsible for the emission from the dopant.
No takes yet. Share an insight, caveat, or question.
Ko et al. (2001) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: