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Xue-yin Jiang

Publications and source records attributed to Xue-yin Jiang.

2 recordsLinked to original sources

[Multiple emissions in organic electroluminescent device using a mixed layer as an emitter].

A organic electroluminescent device has been fabricated by using a mixed layer as an emitter. The configuration of the device is ITO/TPD/TPD: PBD(equimole)/PBD/A1, in which TPD (N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine) and PBD (2-(4'-biphenyl)-5-(4''-tert-butylphenyl)-1,3,4-oxadiazole) are used as hole transport material and electron transport material, respectively. Broad and red-shifted electroluminescent spectra related to the fluorescence of constituent materials were observed. It is suggested that the monomer, exciplex and electroplex emissions are simultaneously involved in EL spectra by comparison of the EL with the PL spectra and decomposition of the EL spectrum. The type of exciplex is the interaction between the excited state TPD (TPD*) and PBD in the ground state, and the type of electroplex is a (D+-A-)* complex by cross-recombination of hole on the charged hole transport molecule (D+) and electron on the charged electron transport molecule (A-). All types of excited states show different formation mechanisms and recombination processes under electric field. The change of emission strengths from monomer and excited complexes lead to a blue-shift of the emissive spectra with an increasing electric field. The maximum luminance and external quantum efficiency of this device are 240 cd x (cm2)(-1) and 0.49%, respectively. The emissions from exciplex or electroplex formation at the organic solid interface generally present a broad and red-shifted emissive band, providing an effective method for tuning of emission color in organic electroluminescent devices.

Biphenyl Compounds↗

[Luminescence properties of Pr(3+) and energy transfer characteristics of Pr(3+)-->Gd(3+) in CaSiO3].

The excitation spectrum and the emission spectrum of Pr3+ in CaSiO3 under the room temperature were studied. The emission spectrum was constituted of three emission bands, corresponding to the emissions of the lowest 4f5d states to the 3H4, 3H6, 1G4 of the 4f2 states. The emission of the 3P0 and 1D2 were not observed. The concentration quenching of Pr3+ was due to the radiative and nonradiative energy transfer. There was energy transfer from Pr3+ to Gd3+, with the transfer rate of 10% of the Pr3+ emission rate.

Calcium Compounds↗