Doping-free hybrid white organic light-emitting diodes with fluorescent blue,phosphorescent green and red emission layers

Industrialized white organic light-emitting diodes (OLEDs) currently require host-guest doping, a complicated process necessitating precise control of the guest concentration to get high efficiency and stability. Two doping-free, hybrid white OLEDs with fluorescent blue, and phosphorescent green and red emissive layers (EMLs) are reported in this work. An ultra-thin red phosphorescent EML was situated in a blue-emitting electron transport layer (ETL), while the ultra-thin green phosphorescent EML was placed either in the ETL (Device 1), or the hole transport layer (HTL) (Device 2). Device 2 exhibits higher efficiency and more stable spectrum due to the enhanced utilization of excitons by ultra-thin green EML at the exciton generation zone within the HTL. Values of current efficiency (CE), power efficiency (PE), and CRI obtained for the optimized hybrid white OLEDs fabricated through a doping-free process were of 23.2 cd/A, 20.5 lm/W and 82 at 1000 cd/m², respectively.     

Detailed Measurements of Nuclear Spin Polarizations in a Single InAlAs Quantum Dot Through Overhauser Shift of Photoluminescence

We investigated optical pumping of nuclear spin polarizations in a single self-assembled In_0.75Al_0.25As/Al_0.3Ga_0.7As quantum dot. The nuclear spin polarization exhibits the abrupt jump and hysteresis in the excitation power dependence at a particular excitation polarization. Measurement of circular polarization rate of the photoluminescence reveals that the abrupt change of the nuclear spin polarization is created mainly by the spin flip-flop process between nuclei and an electron of a positive charged exciton in this single quantum dot. Model calculation explains well the experimentally observed bistable behavior in InAlAs quantum dot. By using this abrupt change, the sign and magnitude of electron and hole g-factors in z-direction are verified.      

Exciton energies of wurtzite CdS nanoparticles

We have determined exciton energies for wurtzite CdS nanoparticles, both theoretically and experimentally. The empirical pseudopotential method has been used to calculate the bulk band structure. The discretization of reciprocal space was considered to get the energy gap and the corresponding exciton energy as a function of the nanoparticles size. The CdS nanoparticles were prepared by colloidal methods and the exciton energies were determined from optical absorption measurements. A good agreement between the calculated and the experimental exciton energies is obtained when an average over the experimental size distribution of the nanoparticles is included in the calculation.     

Photoluminescence of transparent glass-ceramics based on ZnO nanocrystals and co-doped with Eu3+, Yb3+ ions

Glasses of the K₂OZnOAl₂O₃SiO₂ system co-doped with Eu₂O₃ and Yb₂O₃ were prepared by the melt-quenching technique. Transparent zincite (ZnO) glass–ceramics were obtained by secondary heat-treatments at 680–860 °C. At 860 °C, traces of Eu oxyapatite appeared in addition to ZnO nanocrystals. The average crystal size obtained from the X-ray diffraction data was found to range between 14 and 35 nm. Absorption spectra of the initial glasses are composed of an absorption edge and absorption bands due to electronic transitions of Eu³⁺ ions. With heat-treatment, the absorption edge pronouncedly shifts to the visible spectral range. The luminescence properties of the glass and glass-ceramics were studied by measuring their excitation and emission spectra at 300, 78, and 4.2 K. Strong red emission of Eu³⁺ ions dominated by the ⁵D₀–⁷F₂ (612 nm) electric dipole transition was detected. Changes in the luminescence properties of the Eu³⁺-related excitation and emission bands were observed after heat-treatments at 680 °C and 860 °C. The ZnO nanocrystals showed both broad luminescence (400–850 nm) and free-exciton emission near 3.3 eV at room temperature. The upconversion luminescence spectrum of the initial glass was obtained under excitation of the 976 nm laser source.     

Bandwidth and transient analysis of bilayer organic photodetectors

Utilization of organic photodetectors (OPDs) and their applications for assembling on flexible and curved substrates have increased in recent years. However, organic semiconductors suffer from low carrier mobility that demands an optimized design and precise modeling for their applications. The OPDs frequency bandwidth is one of the most important criteria that needs to be investigated carefully. In this paper a comprehensive physical time-domain framework is introduced for bandwidth calculations as well as other several evaluation criteria. This model is verified by experimental measurements. According to the results, increasing the reverse bias voltage boosts the bandwidth of OPD owing to the increase of the carrier mobility. Based on the introduced simulation approach, the trade-off between the bandwidth and the responsivity has been investigated and an efficient design method is also proposed which could effectively improve the OPD performance.     

Impact of defects on exciton diffusion in organic light-emitting diodes

The impact of defect concentration and current density on the effective singlet exciton diffusion length in 4’-bis(carbazol-9-yl)biphenyl (CBP) is quantified by analyzing the electroluminescent characteristics of several sets of OLEDs. The defect concentration and effective diffusion length are determined through fitting of the defect and CBP emission bands in the electroluminescence spectra under constant current operation using an analytical model derived based on the competition between exciton diffusion and energy transfer to defects. Defect concentrations of 3 ± 1 × 10¹⁸ cm⁻³, 2 ± 1 × 10¹⁸ cm⁻³ and 0.3 ± 0.7 × 10¹⁸ cm⁻³ are calculated in three sets of OLEDs, in which the effective diffusion length decreases as the defect concentration increases. Modelling the dependence of the effective diffusion length on defect concentration a “defect free” diffusion length of 4.5 ± 0.3 nm is obtained for CBP singlet excitons in these devices operated under low current density. We also show that the driving voltage scales linearly with the defect concentration.     

Efficient red phosphorescent organic light emitting diodes based on solution processed all-inorganic cesium lead halide perovskite as hole transporting layer

An efficient red phosphorescent organic light emitting diode (PhOLED) has been realized by utilizing a composite hole transporting layer comprised of all-inorganic cesium lead halide perovskite CsPbBr₃ via spin-coating and 1,3-bis(9-carbazolyl) benzene (mCP) by vacuum depositing, in which CsPbBr₃ film is used as a hole transporting layer and mCP plays a dominant role in electron and exciton blocking. And this PhOLED shows a saturated red emission coordinated at CIE (0.65, 0.33) driven at 7.5 V, a maximum brightness of 20,750 cd/m², and a maximum current efficiency of 10.64 cd/A, which is as 1.87 times as that 5.68 cd/A of the reference PhOLEDs based on traditional small organic molecular hole transporting material N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)-benzi (NPB). The electroluminescent (EL) spectra and the energy level alignment of different PhOLEDs are investigated. The enhanced EL performances are ascribed to improved hole injecting and transporting behaviors, and better electron and exciton confinements by introducing the composite hole transporting layer CsPbBr₃/mCP.     

Temperature effect on polaron recombination in conjugated polymers

The microcosmic mechanism of electroluminescence in polymer light emitting diodes (PLEDs) is the recombination of the oppositely charged polarons. In previous studies, it has been demonstrated that the temperature-induced irregular lattice vibration may have non-negligible influence on polaron dynamics. Nevertheless, there are few reports about thermal effect on recombination process between polaron pair, although it is very important for the performance of PLEDs. In this paper, we adopt the modified one-dimensional tight-binding model, including to which the thermal random force, and explore the temperature effect on polaron collision driven by electric field with different strengths. The dynamical simulation is performed by using the non-adiabatic evolution method. The results show that under the influence of electric field, the oppositely charged polarons could recombine into either an exciton with one lattice distortion, or the mixed state of polaron pair and exciton with two lattice distortions. It depends on both field strength and temperature. Anyway, after including temperature effect, a significant improvement of exciton yield is obtained. In addition, the new-formed exciton could perform a random walk along the polymer chain driven by the thermal random force when its strength is large enough. If we further increase the temperature, the stability of exciton would become worse.     

On the exciton profile in OLEDs-seamless optical and electrical modeling

We present a comprehensive model to simulate organic light-emitting devices (OLEDs) that includes a seamless coupling of charges, excitons and photons. The comprehensive model accounts for the position dependent exciton lifetime due to the optical environment in the multilayer OLED structures. We first study the effect of different charge mobilities and quantum efficiencies of the light-emitting material on the exciton profiles. Moreover, we discuss the extension of an optical model to account for the exciton dynamics. This comprehensive optical model is validated and justified on the basis of consistency checks. Namely, we show that our comprehensive optical model can take the cavity effects as seen in simulation results of the comprehensive electrical model into account. The advantage of the comprehensive optical model is a quick and accurate insight into the exciton physics if applied together with a nonlinear least square (NLSQ) fitting method. Finally, we apply the comprehensive optical model with the NLSQ-method in order to extract the exciton profiles from emission spectra of a blue light-emitting polymer diode (PLED) measured at different current levels.     

The working mechanism of organic photovoltaic cell by using copper phthalocyanine as exciton blocking layer

We demonstrate the working mechanism of organic photovoltaic (OPV) cell with copper phthalocyanine (CuPc) as exciton blocking layer (EBL). The new EBL material CuPc, commonly has been used as electron donor in the organic solar cells due to its electron-donating and hole-transporting properties. But here we proves that the α-polymorph CuPc layer can transfer electrons to Al cathode through the half-filled b_1g level, this mechanism is different from that of general EBL material with larger band gap and electron-transporting property, which is based on damage states induced by the heat of evaporating Al.