Defect passivation with natural amino acid molecules is reported, resulting in largely enhanced photovoltages in blade-coated MAPbI₃perovskite solar cells and modules.

Simultaneously achieving high efficiency and high durability in perovskite solar cells is a critical step toward the commercialization of this technology. Inverted perovskite photovoltaic (IP‐PV) cells incorporating robust and low levelized‐cost‐of‐energy (LCOE) buffer layers are supposed to be a promising solution to this target. However, insufficient inventory of materials for back‐electrode buffers substantially limits the development of IP‐PV. Herein, a composite consisting of 1D cation‐doped TiO₂ brookite nanorod (NR) embedded by 0D fullerene is investigated as a top modification buffer for IP‐PV. The cathode buffer is constructed by introducing fullerene to fill the interstitial space of the TiO₂ NR matrix. Meanwhile, cations of transition metal Co or Fe are doped into the TiO₂ NR to further tune the electronic property. Such a top buffer exhibits multifold advantages, including improved film uniformity, enhanced electron extraction and transfer ability, better energy level matching with perovskite, and stronger moisture resistance. Correspondingly, the resultant IP‐PV displays an efficiency exceeding 22% with a 22‐fold prolonged working lifetime. The strategy not only provides an essential addition to the material inventory for top electron buffers by introducing the 0D:1D composite concept, but also opens a new avenue to optimize perovskite PVs with desirable properties.

Solution-processed organo-lead halide perovskites have emerged as promising optical gain media for tunable coherent light sources. The lasing performance is generally determined by the as-synthesized crystal quality. Noble metal nanostructures have been widely utilized to enhance optical responses due to their unique property of localized surface plasmon resonance. Herein, we report a simple method to enhance the near-infrared amplified spontaneous emission (ASE) performance of MAPbI₃ polycrystalline films by solution-processing a PMMA spacer layer and an Au NR-doped PMMA top layer on perovskite thin films. As a result, the ASE threshold of the triple-layer perovskite film was significantly reduced by around 36% and the ASE intensity increased by 13.9-fold, compared to the pristine film. The underlying mechanism was attributed to the combined effects of surface passivation by PMMA and plasmon resonance enhancement of Au NRs. The passivation effect results in suppressing the nonradiative recombination and prolonging excited state decay, which have been investigated by transient absorption and pump–probe measurements. The plasmon effect is systematically studied through distance-dependent and spectra-dependent plasmon enhanced emission. The perovskite films with PMMA and Au NR coating showed great stability for 180 min under intense pulse laser continuous irradiation. The improved ASE performance still remained after leaving the film under the atmosphere for more than one month. We have successfully demonstrated a highly stable and sustained ASE output from MAPbI₃ films under pulse laser excitation. This study provides a general approach for exploring plasmonic nanostructures in combination with polymers in the development and application of low-cost solution-processed semiconductor lasers.

With bay - and ortho -substituted perylenetetracarboxylic diimide derivatives, one-photon and two-photon excited ACQ-to-AIE conversion is realized through simple positional isomerization.

Chiral microlasers hold great promise for optoelectronics from integrated photonic devices to high-density quantum information processing. Despite significant progress in lead-halide perovskite emitters, chiral lasing with high dissymmetry factors (g_lum) has not yet been realized. Here, we demonstrate chiral single-mode microlasers with exceptional stability and tunable emission across the visible range by combining CsPbCl_xBr_3-x perovskite microrods (MRs) with a cholesteric liquid crystal (CLC) layer. The MRs lase via a whispering gallery mode (WGM) microcavity and confer chirality through the encapsulated CLC layer, thus exhibiting circularly polarized lasing with dissymmetry factors reaching 1.62. Importantly, we demonstrate wavelength-tunable high dissymmetry chiral lasers in a broad spectral range by tuning the halide composition and using CLC layers with the desired photonic bandgap (PBG). This facile approach to generate chiral lasing not only is applicable to semiconductor nano- and microcrystals but also paves the way for potential integration into nanoscale photonic devices.