No abstract

A very high hole mobility of 15 cm V s along with negligible hysteresis are demonstrated in transistors with an organic-inorganic perovskite semiconductor. This high mobility results from the well-developed perovskite crystallites, improved conversion to perovskite, reduced hole trap density, and improved hole injection by employing a top-contact/top-gate structure with surface treatment and MoO hole-injection layers.

In this study, we investigate the lasing properties of 4,4′-bis[(N-carbazole)styryl]biphenyl thin films under electrical pumping. The electroluminescent devices incorporate a mixed-order distributed feedback SiO2 grating into an organic light-emitting diode structure and emit blue lasing. The results provide an indication of lasing by direct injection of current into an organic thin film through selection of a high-gain organic semiconductor showing clear separation of the lasing wavelength from significant triplet and polaron absorption and design of a proper feedback structure with low losses at high current densities. This study represents an important advance toward a future organic laser diode technology.

Excess/unreacted lead iodide (PbI2) has been commonly used in perovskite films for the state‐of‐the‐art solar cell applications. However, an understanding of intrinsic degradation mechanisms of perovskite solar cells (PSCs) containing unreacted PbI2 has been still insufficient and, therefore, needs to be clarified for better operational durability. Here, it is shown that degradation of PSCs is hastened by unreacted PbI2 crystals under continuous light illumination. Unreacted PbI2 undergoes photodecomposition under illumination, resulting in the formation of lead and iodine in films. Thus, this photodecomposition of PbI2 is one of the main reasons for accelerated device degradation. Therefore, this work reveals that carefully controlling the formation of unreacted PbI2 crystals in perovskite films is very important to improve device operational stability for diverse opto‐electronic applications in the future.

Organic semiconductor laser operating in the quasi-CW regime at 80 MHz and under 30 ms long pulse photoexcitation is demonstrated.

Device stability of planar perovskite solar cells is improved by virtue of multifunctional BQ additive. The morphology and crystal quality of the perovskite films are improved because BQ slows the rate of perovskite crystal formation. Electron transfer from perovskite to BQ reduces charge-recombination losses, and the oxidizing ability of BQ effectively suppresses the formation of metallic lead and improves device lifetime.

Degradation mechanisms of CH3 NH3 PbI3 -based planar perovskite solar cells (PSCs) are investigated using a thermally stimulated current technique. Hole traps lying above the valence-band edge of the CH3 NH3 PbI3 are detected in PSCs degraded by continuous simulated solar illumination. One source of the hole traps is the photodegradation of CH3 NH3 PbI3 in the presence of water.

A high coverage MASnI3 perovskite film was obtained employing a modified solvent bathing method to realize stable photovoltaic properties.