A charge carrier mobility of polymer films with the time-of-flight(TOF) technique using a fullerene layer was measured and the TOF photocurrent waveform can be remarkably improved.The 80-nm-thick fullerene layer is functioned as a charge-separation layer(CSL) which was placed between ITO electrode and the polymer layer of MEH-PPV(poly[2-methoxy-5-(2'-ethylhexyloxy) 1,4-phenylenevinylene]).In the CSL,the photo-generated holes and electrons can be efficiently separated,resulting in an enhanced current signal and great improvement of TOF waveform.The sample structure with fullerene layer exhibits a great advantage to measure the hole mobilities of polymers with low energy band gap.
A solution-processed zinc oxide (ZnO) thin film as an electron collection layer for polymer solar cells (PSCs) with an inverted device structure was investigated. Power conversion efficiencies (PCEs) of PSCs made with a blend of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) are 3.50% and 1.21% for PSCs with and without the ZnO thin film, respectively. Light intensity dependence of the photocurrent and the capacitance-voltage measurement demonstrate that the increased PCEs are due to the restriction of the strong bimolecular recombination in the interface when a thin ZnO layer is inserted between the polymer active layer and the ITO electrode. These results demonstrate that the ZnO thin film plays an important role in the performance of PSCs with an inverted device structure.
YANG TingBinQIN DongHuanLAN LinFengHUANG WenBoGONG XiongPENG JunBiaoCAO Yong
Efficient deep-red organic light-emitting diodes (OLEDs) were investigated based on the blend of poly[2- methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) with 4,7-bis(5-(7-(9H-carbazol-9-yl)-9,9-dioctyl-9H- fluoren-2-yl)thiophen-2-yl)benzo[c] [1,2,5] thiadiazole (compound 1). By optimizing the blend ratio, the turn-on voltage of the devices was significantly reduced from 4.9 V to 2.4 V. A highest external quantum efficiency of 2.56% was achieved at a blend ratio of 95:5 (wt) for compound 1: MEH-PPV. The CIE coordinate was measured to be (0.70, 0.30), with the luminescence peak at around 680 nm. Based on experimental observations the improvement mechanism is described.
High-brightness and color-stable two-wavelength hybrid white organic light emitting diodes (HWOLEDs) with the configuration of indium tin oxide (ITO)/ N, N, N, N-tetrakis(4-methoxyphenyl)-benzidine (MeO-TPD): tetrafluoro-tetracyanoqino dimethane (F4-TCNQ)/N,N-di(naphthalene-1-yl)-N,N-diphenyl-benzidine (NPB)/ 4,4-N,N-dicarbazolebiphenyl (CBP): iridium (III) diazine complexes (MPPZ) 2 Ir(acac)/NPB/2-methyl-9,10-di(2-naphthyl)anthracene (MADN): p-bis(p-N,N-di-phenyl-aminostyryl)benzene (DSA-ph)/bis(10-hydroxybenzo[h] quino-linato)beryllium complex (Bebq2)/LiF/Al have been fabricated and characterized. The optimal brightness of the device is 69932 cd/m2 at a voltage of 13 V, and the Commission Internationale de l’Eclairage (CIE) chromaticity coordinates are almost constant during a large voltage change of 6–12 V. Furthermore, a current efficiency of 15.3 cd/A at an illumination-relevant brightness of 1000 cd/m2 is obtained, which rolls off slightly to 13.0 cd/A at an ultra high brightness of 50000 cd/m2. We attribute this great performance to wisely selecting an appropriate spacer together with effectively utilizing the combinations of exciton-harvested orange-phosphorescence/blue-fluorescence in the device. Undoubtedly, this is one of the most exciting results in two-wavelength HWOLEDs up to now.