Bo Qiao

Shape-Controlled Synthesis of All-Inorganic CsPbBr3 Perovskite Nanocrystals with Bright Blue Emission

We developed a colloidal synthesis of CsPbBr3 perovskite nanocrystals (NCs) at a relative low temperature (90 °C) for the bright blue emission which differs from the original green emission (∼510 nm) of CsPbBr3 nanocubes as reported previously. Shapes of the obtained CsPbBr3 NCs can be systematically engineered into single and lamellar-structured 0D quantum dots, as well as face-to-face stacking 2D nanoplatelets and flat-lying 2D nanosheets via tuning the amounts of oleic acid (OA) and oleylamine (OM). They exhibit sharp excitonic PL emissions at 453, 472, 449, and 452 nm, respectively. The large blue shift relative to the emission of CsPbBr3 bulk crystal can be ascribed to the strong quantum confinement effects of these various nanoshapes. PL decay lifetimes are measured, ranging from several to tens of nanoseconds, which infers the higher ratio of exciton radiative recombination to the nonradiative trappers in the obtained CsPbBr3 NCs. These shape-controlled CsPbBr3 perovskite NCs with the bright blue emission will be widely used in optoelectronic applications, especially in blue LEDs which still lag behind compared to the better developed red and green LEDs.

Water-resistant, monodispersed and stably luminescent CsPbBr3/CsPb2Br5 core–shell-like structure lead halide perovskite nanocrystals

Lead halide perovskite materials are thriving in optoelectronic applications due to their excellent properties, while their instability due to the fact that they are easily hydrolyzed is still a bottleneck for their potential application. In this work, water-resistant, monodispersed and stably luminescent cesium lead bromine perovskite nanocrystals coated with CsPb2Br5 were obtained using a modified non-stoichiometric solution-phase method. CsPb2Br5 2D layers were coated on the surface of CsPbBr3 nanocrystals and formed a core-shell-like structure in the synthetic processes. The stability of the luminescence of the CsPbBr3 nanocrystals in water and ethanol atmosphere was greatly enhanced by the photoluminescence-inactive CsPb2Br5 coating with a wide bandgap. The water-stable enhanced nanocrystals are suitable for long-term stable optoelectronic applications in the atmosphere.

The Electroluminescence Mechanism of Solution-Processed TADF Emitter 4CzIPN Doped OLEDs Investigated by Transient Measurements

High efficiency, solution-processed, organic light emitting devices (OLEDs), using a thermally-activated delayed fluorescent (TADF) emitter, 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN), are fabricated, and the transient electroluminescence (EL) decay of the device with a structure of [ITO/PEDOT: PSS/4CzIPN 5 wt % doped 4,40-N,N0-dicarbazolylbiphenyl(CBP)/bis-4,6-(3,5-di-4-pyridylphenyl)-2-methylpyrimidine (B4PyMPM)/lithium fluoride (LiF)/Al], is systematically studied. The results shed light on the dominant operating mechanism in TADF-based OLEDs. Electroluminescence in the host–guest system is mainly produced from the 4CzIPN emitter, rather than the exciplex host materials.

Synthesis of ZnO quantum dots and their agglomeration mechanisms along with emission spectra based on ageing time and temperature

The ZnO quantum dots (QDs) were synthesized with improved chemical solution method. The size of the ZnO QDs is exceedingly uniform with a diameter of approximately 4.8 nm, which are homogeneously dispersed in ethanol. The optical absorption edge shifts from 370 nm of bulk material to 359 nm of QD materials due to the quantum size effect, while the photoluminescence peak shifts from 375 nm to 387 nm with the increase of the density of ZnO QDs. The stability of ZnO QDs was studied with different dispersion degrees at 0 °C and at room temperature of 25 °C. The agglomeration mechanisms and their relationship with the emission spectra were uncovered for the first time. With the ageing of ZnO QDs, the agglomeration is aggravated and the surface defects increase, which leads to the defect emission.

Improving the photovoltaic performance of planar heterojunction perovskite solar cells by mixed solvent vapor treatment

The grain size of perovskite films is a key factor to optimize the performance of perovskite photovoltaic devices. Herein, a new route is developed in this paper to prepare CH3NH3PbI3 (MAPbI3) films with a better morphology and crystallization. This method includes the spin coating deposition of perovskite films with a precursor solution of PbI2 and CH3NH3I at the molar ratio 1 : 1 and thermal annealing (TA). The thermal annealing is conducted with a thermal-induced process to realize grain growth with solvent evaporation. In addition, a mixed solvent vapor treatment in acetic acid with chlorobenzene (HAc/CB) improves the morphology and crystallization of films further. As a result, the photovoltaic device based on the perovskite film treated by mixed HAc/CB solvent exhibits the best efficiency of 13.15% in comparison to the control device with 11.44% under AM 1.5G irradiation (100 mW cm−2).

Improving charge transport by the ultrathin QDs interlayer in polymer solar cells

Lead sulfide (PbS) quantum dots (QDs) have been incorporated into PTB7:PC71BM BHJ active layers to fabricate polymer solar cells (PSCs) and gather on the top surface of active layers to form an ultrathin interlayer. The PbS QDs ultrathin interlayer with an appropriate thickness increases the carrier transport capacity, exciton dissociation and reduces the carrier recombination, which leads to a higher short circuit current (Jsc) and fill factor (FF). Finally, the power conversion efficiency (PCE) improves from 7.03% (control devices) to 7.87% with an ultrathin interlayer by doping 5% PbS QDs, while the current density (Jsc) and fill factor (FF) enhances from 13.83 mA cm−2 to 14.81 mA cm−2 and from 68.70% to 70.85%, respectively.

Improving the Charge Carrier Transport and Suppressing Recombination of Soluble Squaraine-Based Solar Cells via Parallel-Like Structure

Small molecule organic solar cells (SMOSCs) have attracted extensive attention in recent years. Squaraine (SQ) is a kind of small molecule material for potential use in high-efficiency devices, because of its high extinction coefficient and low-cost synthesis. However, the charge carrier mobility of SQ-based film is much lower than other effective materials, which leads to the pretty low fill factor (FF). In this study, we improve the performance of SQ derivative-based solar cells by incorporating PCDTBT into LQ-51/PC71BM host binary blend film. The incorporation of PCDTBT can not only increase the photon harvesting, but also provide an additional hole transport pathway. Through the charge carrier mobility and transient photovoltage measurement, we find that the hole mobility and charge carrier lifetime increase in the ternary system. Also, we carefully demonstrate that the charge carrier transport follows a parallel-like behavior.

Highly Efficient and Operational Stability Polymer Solar Cells Employing Nonhalogenated Solvents and Additives

The power conversion efficiencies (PCEs) of potential polymer solar cells have been shown to rapidly exceed 15%. However, these high-performance devices are based on halogenated solvents that pose a significant hazard to the atmospheric environment and human beings. The use of nonhalogenated solvents makes the device less efficient because of its solubility issues. In this work, we report high-efficiency devices utilizing PffBT4T-2OD and [6,6]-phenyl C71 butyric acid methyl ester system from nonhalogenated solvents such as o-xylene ( o-XY) and 1-methylnaphthalene (Me) hydrocarbon solvent. When Me was used as the additive, the PCE of prepared devices improved from 1.83 to 10.13%, which is rather higher than that of the devices processed with traditional solvents combined with chlorobenzene and 1,8-diiodooctane (8.18%). Both atomic force microscopy and transmission electron microscopy confirmed that after nonhalogen solvents are treated, a more finely phase-separated dense morphology of active layers than after halogen solvents. At the same time, grazing incident wide-angle X-ray scattering patterns show that the combination of nonhalogenated solvents o-XY and Me ingeniously formed an ordered crystal and π-π stacking. Also, the stability of devices prepared from nonhalogenated solvents was significantly better than that of halogenated solvents under continuous illumination in the air without encapsulation.