Super-Bright Green Perovskite Light-Emitting Diodes Using Ionic Liquid Additives.

Halide perovskites have potential for use in next-generation low-cost, high-efficiency, and highly color-pure light-emitting diodes (LED) that can be used in various applications, such as flat and flexible displays and solid-state lighting. However, they still lag behind other mature technologies, such as organic LEDs and inorganic LEDs, in terms of performance, particularly brightness. This lag is partly due to the insulating nature of the long-chain organic ligands used to control the perovskite-film morphology. Herein, a 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid (IL) is incorporated as a potential additive with CsPbBr3 perovskite precursors, which results in a super-bright green perovskite light emitting diode (PeLED) achieving a peak luminance of 3.28 × 105  cd m-2 only at a bias voltage of 6 V, with a peak external quantum efficiency of 13.75%. This achievement is the outcome of multirole support from IL that simultaneously enables superior control over the perovskite-film morphology, passivates defects, modifies the band energy levels, and prevents ion migration. Hence, this work demonstrates IL as a novel alternative additive with the potential to outperform conventional long-chain ligands in high-performance PeLED device fabrication.

Unraveling the Charge Transport Mechanism in Mechanochemically Processed Hybrid Perovskite Solar Cell.

The long-term operation of organic-inorganic hybrid perovskite solar cells is hampered by the microscopic strain introduced by the multiple thermal cycles during the synthesis of the material via a solution process route. This setback can be eliminated by a room temperature synthesis scheme. In this work, a mechanochemical synthesis technique at room temperature is employed to process CH3NH3PbI2Br films for fabricating perovskite solar cell devices. The solar cell device has produced a 957 mV Voc, a 16.92 mA/cm2 short circuit current density, and a 10.5% efficiency. These values are higher than the published values on mechanochemically synthesized CH3NH3PbI3. The charge transport properties of the devices are studied using DC conductivity and AC impedance spectroscopy, which show a multichannel transport mechanism having both ionic and electronic contributions. A much smaller defect density in the mechanochemically synthesized hybrid perovskite material is confirmed. A polarization assisted recombination mechanism is observed to have a dominant effect on the overall charge transport mechanism. However, no obvious grain boundary and intralayer lattice defect related responses are found in the perovskite layer. Interfacial charge transport and recombination are found to show major effects on both the temperature dependent and illumination dependent impedance spectra.

Methylammonium Lead Iodide Incorporated Poly(vinylidene fluoride) Nanofibers for Flexible Piezoelectric-Pyroelectric Nanogenerator.

This work introduces a piezoelectric-pyroelectric nanogenerator (P-PNG) based on methylammonium lead iodide (CH3NH3PbI3) incorporated electrospun poly(vinylidene fluoride) (PVDF) nanofibers that are able to harvest mechanical and thermal energies. During the application of a periodic compressive contact force at a frequency of 4 Hz, an output voltage of ∼220 mV is generated. The P-PNG has a piezoelectric coefficient (d33) of ∼19.7 pC/N coupled with a high durability (60 000 cycles) and quick response time (∼1 ms). The maximum generated output power density (∼0.8 mW/m2) is sufficient to charge up a variety of capacitors, with the potential to replace an external power supply to drive portable devices. In addition, upon exposure to cyclic heating and cooling at a temperature of 38 K, a pyroelectric output current of 18.2 pA and a voltage of 41.78 mV were achieved. The fast response time of 1.14 s, reset time of 1.25 s, and pyroelectric coefficient of ∼44 pC/m2 K demonstrate a self-powered temperature sensing capability of the P-PNG. These characteristics make the P-PNG suitable for flexible piezoelectric-pyroelectric energy harvesting for self-powered electronic devices.

Organo-Lead Halide Perovskite Induced Electroactive ß-Phase in Porous PVDF Films: An Excellent Material for Photoactive Piezoelectric Energy Harvester and Photodetector.

Methylammonium lead iodide (CH3NH3PbI3) (MAPI)-embedded ß-phase comprising porous poly(vinylidene fluoride) (PVDF) composite (MPC) films turns to an excellent material for energy harvester and photodetector (PD). MAPI enables to nucleate up to ∼91% of electroactive phase in PVDF to make it suitable for piezoelectric-based mechanical energy harvesters (PEHs), sensors, and actuators. The piezoelectric energy generation from PEH made with MPC film has been demonstrated under a simple human finger touch motion. In addition, the feasibility of photosensitive properties of MPC films are manifested under the illumination of nonmonochromatic light, which also promises the application as organic photodetectors. Furthermore, fast rising time and instant increase in the current under light illumination have been observed in an MPC-based photodetector (PD), which indicates of its potential utility in efficient photoactive device. Owing to the photoresponsive and electroactive nature of MPC films, a new class of stand-alone self-powered flexible photoactive piezoelectric energy harvester (PPEH) has been fabricated. The simultaneous mechanical energy-harvesting and visible light detection capability of the PPEH is promising in piezo-phototronics technology.