Tunable Emission Research Articles

Photoluminescence-Tunable organic phosphine cuprous halides clusters for X-ray scintillators and white light emitting diodes

Low-dimensional cuprous clusters demonstrate fascinating luminescent properties due to their uniquely diversified charge transfer excited states, which imply it could be ideal candidate for multifunctional applications, such as X-ray scintillators and white light emitting diodes (WLED). However, it is still challenge for low-dimensional cuprous clusters that how to regulate the emission performance to meet the requirements of the specific applications. In this work, we prepared a series of luminescent organic cuprous iodide clusters, (IPP)CuI2 and (IPP)2CuI3, which show tunable emission property by simply component regulation. The (IPP)CuI2 with IPP: CuI = 1: 0.75 show the best scintillator property with super-low detection limit of 62.29 nGy/s and high light yields of 75793.83 photons/MeV which is far beyond most organic copper halide scintillators. A series of clear digital radiography (DR) with high spatial resolution of 10.2 lp/mm and a reconstructed 3D model based on computed tomography (CT) were successfully obtained by the prepared scintillation screen. Moreover, the single-component WLED based on accurately component regulation (IPP)CuI2 with IPP: CuI = 1: 0.99 exhibits pure white emission with a high CRI (color rendering index) of 82. The luminescence mechanism of charge transfer excited states in tunable emission (IPP)CuI2 was also investigated. Our works not only provide a kind of ideal materials applied for high-performance single-component WLED and scintillator but also reveal the large potential of low-dimensional organic cuprous halides as luminescent material for multifunctional applications.

Introduction of Organic Dyes into Cadmium(II) MOF for Tunable Light Emission and Highly Sensitive Probing Antibiotics

AbstractA honeycomb porous cadmium(II) metal–organic framework {[Cd(L)(H2O)] ⋅ NMP ⋅ 5H2O}n (1, H2L=1‐(4‐carboxyphenyl)‐1H‐pyrazole‐3‐carboxylic acid and NMP=1‐methyl‐2‐pyrrolidinone) was obtained using the solvothermal method. The luminescent molecules rhodamine B (RhB) and fluorescein (FL) were encapsulated in 1 using the immersion method to prepare RhB@1 and FL@1 dual emission composites. Additionally, a series of RhBx/FL1‐x@1 composites with varying luminescence properties were generated by altering the molar ratio of RhB to FL. Furthermore, the photoluminescence of RhB@1 and FL@1 was demonstrated to be caused by photoelectron transfer and fluorescence resonance energy transfer from 1 to the encapsulated guest module. Notably, RhB@1 showed the considerable improvement in fluorescence selectivity and detection limit (10−6 M) for metronidazole and dimetronidazole with remarkable recyclability.

Efficient and stable hybrid perovskite-organic light-emitting diodes with external quantum efficiency exceeding 40 per cent

Light-emitting diodes (LEDs) based on perovskite semiconductor materials with tunable emission wavelength in visible light range as well as narrow linewidth are potential competitors among current light-emitting display technologies, but still suffer from severe instability driven by electric field. Here, we develop a stable, efficient and high-color purity hybrid LED with a tandem structure by combining the perovskite LED and the commercial organic LED technologies to accelerate the practical application of perovskites. Perovskite LED and organic LED with close photoluminescence peak are selected to maximize photon emission without photon reabsorption and to achieve the narrowed emission spectra. By designing an efficient interconnecting layer with p-type interface doping that provides good opto-electric coupling and reduces Joule heating, the resulting green emitting hybrid LED shows a narrow linewidth of around 30 nm, a peak luminance of over 176,000 cd m−2, a maximum external quantum efficiency of over 40%, and an operational half-lifetime of over 42,000 h.

Fabrication of red-emitting perovskite LEDs by stabilizing their octahedral structure.

Light-emitting diodes (LEDs) based on metal halide perovskites (PeLEDs) with high colour quality and facile solution processing are promising candidates for full-colour and high-definition displays1-4. Despite the great success achieved in green PeLEDs with lead bromide perovskites5, it is still challenging to realize pure-red (620-650 nm) LEDs using iodine-based counterparts, as they are constrained by the low intrinsic bandgap6. Here we report efficient and colour-stable PeLEDs across the entire pure-red region, with a peak external quantum efficiency reaching 28.7% at 638 nm, enabled by incorporating a double-end anchored ligand molecule into pure-iodine perovskites. We demonstrate that a key function of the organic intercalating cation is to stabilize the lead iodine octahedron through coordination with exposed lead ions and enhanced hydrogen bonding with iodine. The molecule synergistically facilitates spectral modulation, promotes charge transfer between perovskite quantum wells and reduces iodine migration under electrical bias. We realize continuously tunable emission wavelengths for iodine-based perovskite films with suppressed energy loss due to the decrease in bond energy of lead iodine in ionic perovskites as the bandgap increases. Importantly, the resultant devices show outstanding spectral stability and a half-lifetime of more than 7,600 min at an initial luminance of 100 cd m-2.

Optical Property Control by the Interligand Charge Transfer Excited State in Brominated Homoleptic and Heteroleptic Aluminum Dinuclear Triple-Stranded Helicates.

The utilization of aluminum, an abundant and inexpensive element, for the synthesis of novel functional complexes is extremely important, but the design and control of photofunctionality are still unexplored. In this study, we focused on our previously developed dinuclear triple-stranded helicates incorporating two aluminum ions (ALPHY) to synthesize both homoleptic and heteroleptic complexes with bromine atoms at the 3-position of the pyrrole moiety in the Schiff base ligands. The brominated Schiff base ligands were reacted with AlCl3 to synthesize homoleptic complexes, while different ligands were mixed to prepare heteroleptic complexes. Single-crystal X-ray structural analysis revealed the structures of these novel complexes. We found that increasing the degree of bromination resulted in a tunable emission color, shifting progressively from 550 (yellow) to 566 nm (orange). Optical resolution of the complexes facilitated the observation of mirror-image circular dichroism and circularly polarized luminescence. Furthermore, employing ultrafast spectroscopy techniques, we have elucidated that the optical properties are governed by the interligand charge transfer (ILCT) among the three ligands. The formation of heteroleptic complexes induces the ILCT state even in nonpolar environments, thereby accelerating nonradiative decay and intersystem crossing. These findings mark significant advancements in photofunctional materials based on multinuclear complexes.

New PMMA-InP/ZnS nanohybrid coatings for improving the performance of c-Si photovoltaic cells

Abstract Luminescent down-shifting (LDS) nanohybrid films are considered a potential solution to match the absorption spectrum of photovoltaic (PV) cells with the AM1.5 solar spectrum. LDS films were prepared by spin-coating polymethyl methacrylate (PMMA) doped with indium phosphide/zinc sulfide (InP/ZnS) quantum dots (QDs). The effect of doping concentration was investigated using X-ray diffraction, thermogravimetric analysis, transmission, and fluorescence spectroscopy. The results demonstrated that all PMMA LDS nanohybrid films were amorphous and exhibited thermal and chemical stability for all the doping concentrations of QDs. The optimal doping concentration was 0.06 wt%, demonstrating a tunable emission of the highest fluorescence quantum yield of 92% and the lowest reabsorption effect. This film showed the maximum enhancement of the efficiency of c-Si PV cells by 24.28% due to the down-conversion of ultraviolet A (UVA) portion of solar spectrum (320–400 nm) to match the sensitivity of c-Si PV cells. The implications of these results are significant for advancing affordable and clean energy in alignment with important sustainable development goals.

Rational Design of NIR-II Emitting Conjugated Polymer Derived Nanoparticles for Image-Guided Cancer Interventions.

Due to the reduced absorption, light scattering, and tissue autofluorescence in the NIR-II (1000-1700nm) region, significant efforts are underway to explore diverse material platforms for in vivo fluorescence imaging, particularly for cancer diagnostics and image-guided interventions. Of the reported imaging agents, nanoparticles derived from conjugated polymers (CPNs) offer unique advantages to alternative materials including biocompatibility, remarkable absorption cross-sections, exceptional photostability, and tunable emission behavior independent of cell labeling functionalities. Herein, the current state of NIR-II emitting CPNsare summarized and structure-function-property relationships are highlighted that can be used to elevate the performance of next-generation CPNs. Methods for particle processing and incorporating cancer targeting modalities are discussed, as well as detailed characterization methods to improve interlaboratory comparisons of novel materials. Contemporary methods to specifically apply CPNs for cancer diagnostics and therapies are then highlighted. This review not only summarizes the current state of the field, but offers future directions and provides clarity to the advantages of CPNs over other classes of imaging agents.

Impact of Tamm plasmon structures on fluorescence and optical nonlinearity of graphene quantum dots

Graphene Quantum Dots (GQDs) are crucial in biomedicine for sensitive biosensing and high-resolution bioimaging and in photonics for their nonlinear optical properties. Integrating GQDs with photonic structures enhances optical properties by optimizing light-matter interactions and enabling precise control over their emission wavelengths. In this work, we explore a facile synthesis method for GQDs by pulsed laser irradiation in chlorobenzene and highlight the transformative potential of Tamm Plasmon Cavity (TPC) structures for tuning and amplifying the photoluminescence and nonlinear optical properties of GQDs. The characterization of GQDs revealed their exceptional properties, including efficient optical limiting and stable photoluminescence. The study demonstrated that the TPC structure significantly amplifies nonlinear optical effects due to the high light-matter interaction, indicating the potential for advanced optical systems, including optical limiters and nonlinear optical devices. Furthermore, introducing GQDs into the TPC structure leads to a significant enhancement and tuning of fluorescence emission. The Purcell effect, in combination with the confined electromagnetic fields within the TPC, increases the spontaneous emission rate of GQDs and subsequently enhances the fluorescence intensity. This enhanced and tunable fluorescence has exciting implications for high-sensitivity applications such as biosensing and single-molecule detection.

Blue Emission from Metal Halide Perovskites: Strategies and Applications

Luminescent metal halides, as a type of luminescent semiconductor material, offer advantages that fulfill the requirements of emerging light source devices, such as high luminescence efficiency, good thermal stability, and tunable colorful emission. Blue light being one of the three primary colors plays a crucial role in the field of lighting and colorful displays. However, the progress in device performance of blue‐light materials lags behind that of green and red‐light materials. Currently, there have been numerous reports on metal halide perovskite blue‐light materials, but a comprehensive review on the development and performance control of blue‐light metal halides is yet to be found. This paper provides a comprehensive summary of the design strategies and luminescence mechanisms of blue‐light perovskites with various luminescence centers, as well as their application progress in the fields of light‐emitting diodes (LEDs), X‐ray scintillators, information anti‐counterfeiting and encryption. It also explores possible directions for subsequent performance improvement. This work aims to offer valuable insights and recommendations for the future development of blue‐light metal halides, with significant implications for the fabrication of novel blue light devices and advancements in detection technology.

Linker Engineering toward Tunable Emission Behavior of Porous Interpenetrated Zr-Organic Frameworks.

Conjugated molecules with donor-acceptor-donor (D-A-D) moieties have garnered significant attention for their ability to form luminescent metal-organic frameworks (LMOFs). D-A-D molecules feature tunable bandgaps, which can be varied systematically to control the fluorescence wavelength of LMOFs. In this study, we prepared and characterized the fluorescence properties of two porous interpenetrated Zr-organic frameworks (PIZOFs) constructed using 4,4'-(benzo[c][1,2,5]selenadiazole-4,7-diylbis(ethyne-2,1-diyl))dibenzoic acid (L-Se) or 4,4'-(benzo[c][1,2,5]thiadiazole-4,7-diylbis(ethyne-2,1-diyl))dibenzoic acid (L-S) as linkers. The corresponding MOFs are denoted as PIZOF-Se and PIZOF-S, respectively. Through our investigation, we explored the correlation between the structure of the frameworks and their respective optical properties. Our findings revealed that there are distinct differences in the fluorescence properties of the two PIZOFs. Specifically, the fluorescence of PIZOF-S is red-shifted from that characteristic of the corresponding linker, L-S. By contrast, the fluorescence of PIZOF-Se is substantially blue-shifted from that of linker L-Se. The emission of mixed-linker MOFs is explored by combining L-S or L-Se with structurally analogous, but nonfluorescent linker, 4,4'-((perfluoro-1,4-phenylene)bis(ethyne-2,1-diyl))dibenzoic acid (L-F). Based on steady-state and time-resolved photoluminescence experiments, as well as confocal fluorescence microscopy combined with fluorescence lifetime imaging (FILM), we demonstrated that linker engineering is an effective method to tune the emission behavior of LMOFs.

Tunable Multicolor Emission and High Thermal Stability in Single‐Matrix Luminescent Crystals Based on Calcium Perovskites for Advanced Solid‐State Lighting Applications

AbstractThe development of environmentally friendly full‐inorganic luminescent materials with tunable emission properties and exceptional thermal stability is of paramount importance for applications in optoelectronic devices, solid‐state lighting, and anti‐counterfeiting technologies. In this study, a novel luminescent crystal based on calcium perovskites Cs2CaCl4·2H2O (CCCH) are explored using a hydrothermal method. Simultaneous co‐doping of CCCH with Sn2+ and Mn2+ yields the s‐p transition‐induced cyan light from Sn2+ and d‐d transition‐induced yellow light from Mn2+. It demonstrates effective energy transfer from self‐trapped exciton (STE) of matrix CCCH and s‐p transition of Sn2+ to Mn2+, synergizing composite white lights with tunable colors. Furthermore, the incorporation of Sn2+ into CCCH introduces a red shift from blue to cyan emission with a remarkable enhancement in luminescent intensity by a factor of 12 times. The crystal orbital Hamiltonian populations (─COHP) calculations revealed the crucial role of Mn2+ in lattice stability, as evidenced by the decomposition temperature exceeding 305 °C for CCCH:Sn2+,Mn2+ whereas 210 °C for undoped CCCH matrix. This research provides a comprehensive investigation of the luminescent properties of CCCH:Sn2+,Mn2+ crystal, holding significant promise for practical technological advancements in lighting and anti‐counterfeiting technologies.

Rational Design of Pyrido[3,2-b]indolizine as a Tunable Fluorescent Scaffold for Fluorogenic Bioimaging.

Novel fluorescent scaffolds are highly demanding for a wide range of applications in biomedical investigation. To meet this demand, the pyrido[3,2-b]indolizine scaffold was designed as a versatile organic fluorophore. With the aid of computational modeling, fluorophores offering tunable emission colors (blue to red) were constructed. Notably, constructed fluorophores absorb lights in the visible range (>400 nm) despite their small sizes (<300 g/mol). Among the fluorophores was discovered a highly fluorogenic fluorophore with a unique turn-on property, 1, and it was developed into a washing-free bioprobe for visualizing cellular lipid droplets in living cells. Furthermore, motivated by the core's compact size and structural analogy to indole, unprecedented tryptophan-analogous fluorogenic unnatural amino acids were constructed and incorporated into fluorogenic peptide probes for monitoring peptide-protein interactions.

A Near-Infrared Fluorescent Dye with Tunable Emission Wavelength and Stokes Shift as a High-Sensitivity Cysteine Nanoprobe for Monitoring Ischemic Stroke.

Sulfur-substituted dicyanomethylene-4H-chromene (DCM) derivatives based on the intramolecular charge transfer (ICT) mechanism were designed as near-infrared (NIR) fluorescent dyes. Using the Knoevenagel condensation method, the S-DCM-OH(835) fluorescence dye was synthesized, which had an emission wavelength exceeding 800 nm and 220 nm of a Stokes shift. Compared to commercial ICG, S-DCM-OH(835) was not only synchronized in emission wavelength but also far superior in Stokes shifts. These advantages made the design of S-DCM-NIR(835) based on this dye potentially valuable for biological applications. Based on this chemical structure, a fluorescent S-DCM-NIR(835) nanoprobe with a mean diameter of 17.69 nm was fabricated as the NIR imaging nanoprobe. Results showed that the nanoprobe maintained the high-specificity identification of cysteine (Cys) via the Michael addition reaction, with the detection limitation of 0.11 μM endogenous Cys. More importantly, in an ischemic stroke mouse model, the S-DCM-NIR(835) nanoprobe could monitor the Cys concentration change at stroke lesion due to the disruption of Cys metabolism under the ischemic stroke condition. Such a S-DCM-NIR(835) nanoprobe could not only differentiate the severity of the ischemic stroke using response time but also quantify the concentration of Cys in real-time in vivo.

Ultranarrow Deep-Blue Luminescence of Perovskite Nanocrystals by A-Site Cation Control.

Metal-halide perovskite nanocrystals (NCs) are one of the most promising emitters for the application of display and nanolight sources. The full width at half-maximum (FWHM) of photoluminescence (PL) emission is essential for color purity, which however remains a difficulty to further reduce the FWHM of the perovskite NCs at room temperature. Here, we show the quasi-sphere perovskite NCs with narrow PL emission at a deep-blue wavelength of ∼430 nm; its PL FWHM reaches ∼11 nm at room temperature, owing to the monodispersion in size distribution as well as the symmetric quasi-sphere morphology of NCs releasing the fine structure splitting-induced inhomogeneous broadening. Through regulating A cations with respect to the ratio of FA (or MA)-to-Cs and Cs-to-Pb, the PL emission of the NCs could be tuned from ∼505 to ∼430 nm combined with varied morphologies from large cube to small quasi-sphere. Such spectroscopic and morphological discrepancies are supposed to be attributed to the different crystalline kinetics that is strongly dependent on the synthetic condition. To be specific, in the case of increasing FA (or MA)-to-Cs, the growth rate of CsPbBr3 and FAPbBr3 (or MAPbBr3) perovskites is determined by the reactivity of transient species, while in the case of decreasing the Cs-to-Pb ratio, the growth rate of perovskites is slowed down by the serious reduction of Cs+ in the precursor. This study provides an effective strategy to adjust the emission across from green to deep-blue color and promotes the perovskite NCs with a narrow FWHM, and tunable PL emission facilitates in application of optoelectronic devices.

Multicolour stretchable perovskite electroluminescent devices for user-interactive displays

Wearable displays require mechanical deformability to conform to the skin, as well as long-term stability, multicolour emission and sufficient brightness to enable practically useful applications. However, endowing a single device with all the features remains a challenge. Here we present a rational material design strategy and simple device-manufacturing process for skin-conformable perovskite-based alternating-current electroluminescent (PeACEL) devices. These devices exhibit a narrow emission bandwidth (full-width at half-maximum, <37 nm), continuously tuneable emission wavelength (468–694 nm), high stretchability (400%) and adequate luminance (>200 cd m−2). The approach leverages a new class of perovskite zinc sulfide (PeZS) phosphors, consisting of ZnS phosphors coated with perovskite nanoparticles for electrical excitation via total intraparticle energy transfer. This strategy results in pure red and green emissions and expands the colour gamut of powder-based ACEL devices by 250%. Moreover, our processing technique facilitates the integration of PeACEL displays with wearable electronics, enabling applications in dynamic interactive displays and visual real-time temperature monitoring. These PeACEL displays offer new routes in flexible electronics and hold potential for the development of efficient artificial skins, robotics and biomedical monitoring devices.

High-efficiency red perovskite quantum dot light-emitting diodes via an effective cation exchange method for tunable emission wavelength

The utilization of perovskite quantum dots (PQDs) in photoelectric devices is indeed an area of intense research due to their advantageous properties such as tunability of visible light and efficient light emission. In this study, mixed CsPbI3 and FAPbI3 PQD dispersions were successfully employed for cation exchange to prepare red-color Cs1−xFAxPbI3 PQD with the photoluminescence (PL) wavelength from 689 nm (x = 0) to 778 nm (x = 1). It is also found that the aggregation of Cs1−xFAxPbI3 PQD films were strongly dependent on x. When x from 0 to 0.6, the holes in PQD thin films were gradually improved. On the opposite, when x > 0.6, the PQDs thin films returned more and more holes due to an excess of FA + cations. The resulting Cs1-xFAxPbI3 PQD based light-emitting diodes (LEDs) also demonstrated tunable emission wavelengths, and it is worth mentioning that the maximum external quantum efficiency (EQE) of 11.22 % was achieved with an emission wavelength of 758 nm when x = 0.6.

Evaluating Pb-based and Pb-free Halide Perovskites for Solar-Cell Applications: A Simulation Study

Metal halide Pb-based and Pb-free perovskite crystal structures are an essential class of optoelectronic materials due to their significant optoelectronic properties, optical absorption and tuneable emission spectrum properties. However, the most efficient optoelectronic devices were based on the Pb as a monovalent cation, but its toxicity is a significant hurdle for commercial device applications. Thus, replacing the toxic Pb with Pb-free alternatives (such as tin (Sn)) for diverse photovoltaic and optoelectronic applications is essential. Moreover, replacing the volatile methylammonium (MA) with cesium (Cs) leads to the development of an efficient perovskite absorber layer with improved optical & thermal stability and stabilized photoconversion efficiency. This paper discusses the correlation between the experimental and theoretical work for the Pb-based and Pb-free perovskites synthesised using the hot-injection method at different temperatures. Here, simulation is also carried out using the help of SCAPS-1D software to study the effect of various parameters of CsSnI3 and CsPbI3 layers on solar cell performance. This experimental and theoretical comparative study of the Hot-injection method synthesised CsPbI3 and CsSnI3 perovskites is rarely investigated for optoelectronic applications.

Multi-dimensional hydrogen bonds regulated emissions of single-molecule system enabling surficial hydrophobicity/hydrophilicity mapping

Constructing multi-dimensional hydrogen bond (H-bond) regulated single-molecule systems with multi-emission remains a challenge. Herein, we report the design of a new excited-state intramolecular proton transfer (ESIPT) featured chromophore (HBT-DPI) that shows flexible emission tunability via the multi-dimensional regulation of intra- and intermolecular H-bonds. The feature of switchable intramolecular H-bonds is induced via incorporating several hydrogen bond acceptors and donors into one single HBT-DPI molecule, allowing the “turn on/off” of ESIPT process by forming isomers with distinct intramolecular H-bonds configurations. In response to different external H-bonding environments, the obtained four types of crystal/cocrystals vary in the contents of isomers and the molecular packing modes, which are mainly guided by the intermolecular H-bonds, exhibiting non-emissive features or emissions ranging from green to orange. Utilizing the feature of intermolecular H-bond guided molecular packing, we demonstrate the utility of this fluorescent material for visualizing hydrophobic/hydrophilic areas on large-scale heterogeneous surfaces of modified poly(1,1-difluoroethylene) (PVDF) membranes and quantitatively estimating the surface hydrophobicity, providing a new approach for hydrophobicity/hydrophilicity monitoring and measurement. Overall, this study represents a new design strategy for constructing multi-dimensional hydrogen bond regulated ESIPT-based fluorescent materials that enable multiple emissions and unique applications.

Multiple photofluorochromic luminogens via catalyst-free alkene oxidative cleavage photoreaction for dynamic 4D codes encryption

Controllable photofluorochromic systems with high contrast and multicolor in both solutions and solid states are ideal candidates for the development of dynamic artificial intelligence. However, it is still challenging to realize multiple photochromism within one single molecule, not to mention good controllability. Herein, we report an aggregation-induced emission luminogen TPE-2MO2NT that undergoes oxidation cleavage upon light irradiation and is accompanied by tunable multicolor emission from orange to blue with time-dependence. The photocleavage mechanism revealed that the self-generation of reactive oxidants driving the catalyst-free oxidative cleavage process. A comprehensive analysis of TPE-2MO2NT and other comparative molecules demonstrates that the TPE-2MO2NT molecular scaffold can be easily modified and extended. Further, the multicolor microenvironmental controllability of TPE-2MO2NT photoreaction within polymer matrices enables the fabrication of dynamic fluorescence images and 4D information codes, providing strategies for advanced controllable information encryption.

Distributed Feedback Lasing in Thermally Imprinted Phase‐Stabilized CsPbI3 Thin Films

AbstractAll‐inorganic cesium lead halide perovskites (CsPbX3, with X = I, Br, Cl) are of great interest for light‐emitting diodes and lasers, as they promise improved thermal stability compared to their organic–inorganic analogues. However, among this family of materials, CsPbI3 shows a detrimental phase instability that causes the perovskite to convert to a thermodynamically preferred non‐perovskite phase (yellow phase) at room temperature. In fact, reports on lasers using thin films of CsPbI3 as gain medium are missing, as of yet. Here, the first distributed feedback (DFB) lasers based on CsPbI3 thin films are presented with a resonator directly patterned into the perovskite by thermal nanoimprint. This breakthrough is unlocked by the additive polyvinyl pyrrolidone (PVP), that affords the formation of perovskite layers consisting of phase stable γ‐CsPbI3 nanocrystals, that are even preserved during thermal imprint at 170 °C. The DFB lasers show a low lasing threshold of 45 µJ cm−2 at room temperature under optical pumping and a tunable emission in the deep red spectral region between 714.1 to 723.4 nm. It is anticipated that the findings of this work will have a broad relevance for future electrically driven perovskite lasers and for light‐emitting diodes based on CsPbI3 as active medium.