Search Results (56)

Two-dimensional (2D) metal-halide perovskites with highly efficient room-temperature phosphorescence (RTP) are rare due to their complex structures and intricate intermolecular interactions. In this study, by varying the alkyl chain length in organic amines, we synthesized two 2D metal-halide perovskites, namely 4-POMACC and 4-POEACC, both of which exhibit significant RTP emission. Notably, 4-POMACC demonstrates a stronger green RTP emission with a significantly longer lifetime (254 ms) and a higher photoluminescence quantum yield (9.5%) compared to 4-POEACC. A thorough investigation of structural and optical properties reveals that shorter alkyl chains can enhance the optical performance due to reduced molecular vibrations and more effective exciton recombination. Computational calculations further show that the smaller energy gap between S₁ and T_n in 4-POMA facilitates intersystem crossing, thereby improving RTP performance. Based on their remarkable phosphorescence properties, we demonstrated their applications in information encryption. This work offers a novel design strategy that could inspire the development of next-generation RTP materials. Full article

The most commonly used optical oxygen sensing materials are phosphorescent molecules and functionalized nanocrystals. Many exploration studies on oxygen sensing have been carried out using the fluorescence or phosphorescence of semiconductor nanomaterials. Lead halide perovskite nanocrystals, a new type of ionic semiconductor, have excellent optical properties, making them suitable for use in optoelectronic devices. They also show promising applications in analytical sensing and biological imaging, especially manganese-doped perovskite nanocrystals for optical oxygen sensing. As a class of materials with diverse sources, copper iodide cluster semiconductors have rich structural and excellent luminescent properties, and have attracted attention in recent years. These materials have adjustable optical properties and sensitive stimulus response properties, showing great potential for optical sensing applications. This review paper provides a brief introduction to traditional oxygen sensing using organic molecules and introduces research on oxygen sensing using novel luminescent semiconductor materials, perovskite metal halides and copper iodide hybrid materials in recent years. It focuses on the mechanism and application of these materials for oxygen sensing and evaluates the future development direction of these materials for oxygen sensing. Full article

The use of organic halide salts to passivate metal halide perovskite (MHP) surface defects has been studied extensively. Passivating the surface defects of the MHP is of critical importance for realizing highly efficient and stable perovskite solar cells (PSCs). Here, the successful application of a multifunctional organic salt, methyltriphenylphosphonium iodide (MTPPI), used as a passivation additive for grain boundary defects and as a molecular sealing layer in terms of stabilization, has been used to stabilize the mixed cation perovskite RbCsMAFA-PbIBr. To assess the passivating and stabilizing effects of MTPPI on RbCsMAFA-PbIBr PSCs, maximum power point tracking (MPPT) was applied as the most realistic and closest-to-application condition for the ageing test. Here, perovskite solar cells were aged under a light source yielding an excitation intensity corresponding to one sun with maximum power point tracking, which was interrupted periodically by current–voltage sweeps. This allowed for the extraction of all photovoltaic parameters necessary for a proper understanding of the ageing process. The MTPPI additive can donate iodine anions to halide vacancies and compensate a negative surface excess charge with cation interactions. On top of this, the large and bulky methyltriphenylphosphonium (MTPP⁺) cation may block both the escape of volatile perovskite components and the ingress of oxygen and water vapour. These collective roles of MTPPI have improved both the efficiency and stability of the solar cells compared to the reference without passivation additives. Full article

This review provides an analysis of non-perovskite hybrid halides of coinage metals templated by metal–organic cations (CCDC November 2023). These materials display remarkable structural diversity, from zero-dimensional molecular complexes to intricate three-dimensional frameworks, allowing fine-tuning of their properties. A total of 208 crystal structures, comprising haloargentates, mixed-metal haloargentates, and halocuprates, are categorized and examined. Their potential in photocatalysis is discussed. Special attention is given to the structural adaptability of these materials for the generation of functional interfaces. This review highlights key compounds and aims to inspire further research into optimizing hybrid halides for advanced technological applications. Full article

Halide perovskite has shown great potential in photocatalysis owing to its diversity, suitable energy band alignment, rapid charge transfer, and excellent optical properties. However, poor stability, especially under humid conditions, hinders their practical application in photocatalysis. In this work, we report the encapsulation of inorganic–organic hybrid perovskite QDs into MIL-101(Cr) through an in situ growth strategy to prepare a series of MAPbBr₃@MIL-101(Cr) (MA = CH₃NH₃⁺) composites. The perovskite precursors, i.e., MABr and PbBr₂, were successively introduced into the pores of MOF, where the perovskite quantum dots were self-assembled in the confined environment. In photocatalytic CO₂ reduction, 11%MAPbBr₃@MIL-101(Cr) composite displayed the best performance among the composites with a total CO and CH₄ yield of 875 μmol g⁻¹ in 9 h, which was 8 times higher than that of the pure MAPbBr₃. Such high gas production efficiency could be maintained for 78 h at least without structural and morphologic decomposition. The remarkable stability and catalytic activity of composites are mainly due to the synergistic effect and improved electron transfer between MAPbBr₃ and MIL-101(Cr). Moreover, these composites revealed a novel mechanism, showing switched CH₄ selectivity with the controlling of the perovskite location and contents. Those with perovskites encapsulated in the mesopores of MIL-101(Cr) were more preferential for CO production, while those with perovskites encapsulated in both meso- and micropores could produce CH₄ dominantly. Full article

Organic–inorganic hybrid metal halide perovskites are poised to revolutionize the next generation of photovoltaics with their exceptional optoelectronic properties and compatibility with low-cost and large-scale fabrication methods. Since perovskite tends to degrade over short time intervals due to various parameters (oxygen, humidity, light, and temperature), advanced characterization methods are needed to understand their degradation mechanisms. In this context, investigation of the electrical and optoelectronic properties of several perovskite mini-modules was performed by means of photo- and electroluminescence imaging as well as Dark Lock-In Thermography methods. Current–voltage curves at periodic time intervals and External Quantum Efficiency measurements were implemented alongside other measurements to reveal correlations between the electrical and radiative properties of the solar cells. The different imaging techniques used in this study reveal the changes in radiative emission processes and how those are correlated with performance. Alongside the indoor optoelectronic characterization of perovskite reference samples, the outdoor monitoring of two perovskite modules of the same structure for 23 weeks is reported. Significant performance degradation is presented outdoors from the first week of testing for both samples under test. The evolution of the major electrical characteristics of the mini-modules and the diurnal changes were studied in detail. Finally, dark storage recovery studies after outdoor exposure were implemented to investigate changes in the major electrical parameters. Full article

This study presents the structure and optoelectronic properties of a perovskite-like (PEA)₂PbBr₃Cl material on an AlN/sapphire substrate heterostructure prepared using spin coating. The AlN/sapphire substrate comprised a 2 μm thick AlN epilayer on a sapphire wafer deposited via metal–organic chemical vapor deposition (MOCVD). The peak position of (PEA)₂PbBr₃Cl photoluminescence (PL) on the AlN/sapphire substrate heterostructure was 372 nm. The emission wavelength ranges of traditional lead halide perovskite light-emitting diodes are typically 410 to 780 nm, corresponding to the range of purple to deep red as the ratio of halide in the perovskite material changes. This indicates the potential for application as a UV perovskite light-emitting diode. In this study, we investigated the contact characteristics between Ag metal and the (PEA)₂PbBr₃Cl layer on an AlN/sapphire substrate heterostructure, which improved after annealing in an air environment due to the tunneling effect of the thermionic-field emission (TFE) mechanism. Full article

Recently, the utilization of metal halide perovskites in sensing and their application in environmental studies have reached a new height. Among the different metal halide perovskites, cesium lead halide perovskites (CsPbX₃; X = Cl, Br, and I) and composites have attracted great interest in sensing applications owing to their exceptional optoelectronic properties. Most CsPbX₃ nanostructures and composites possess great structural stability, luminescence, and electrical properties for developing distinct optical and photonic devices. When exposed to light, heat, and water, CsPbX₃ and composites can display stable sensing utilities. Many CsPbX₃ and composites have been reported as probes in the detection of diverse analytes, such as metal ions, anions, important chemical species, humidity, temperature, radiation photodetection, and so forth. So far, the sensing studies of metal halide perovskites covering all metallic and organic–inorganic perovskites have already been reviewed in many studies. Nevertheless, a detailed review of the sensing utilities of CsPbX₃ and composites could be helpful for researchers who are looking for innovative designs using these nanomaterials. Herein, we deliver a thorough review of the sensing utilities of CsPbX₃ and composites, in the quantitation of metal ions, anions, chemicals, explosives, bioanalytes, pesticides, fungicides, cellular imaging, volatile organic compounds (VOCs), toxic gases, humidity, temperature, radiation, and photodetection. Furthermore, this review also covers the synthetic pathways, design requirements, advantages, limitations, and future directions for this material. Full article

Perovskite-based metal oxide phototransistors have emerged as promising photodetection devices owing to the superior optoelectronic properties of perovskite materials and the high carrier mobility of metal oxides. However, high dark current has been one major problem for this type of device. Here, we studied the dark current behaviors of phototransistors fabricated based on the Indium Gallium Zinc Oxide (IGZO) channel and different perovskite materials. We found that depositing organic–inorganic hybrid perovskites materials (MAPbI₃/FAPbI₃/FA_0.2MA_0.8PbI₃) on top of IGZO transistor can increase dark current from ~10⁻⁶ mA to 1~10 mA. By contrast, we observed depositing an inorganic perovskite material, CsPbI₃, incorporated with PCBM additive can suppress the dark current down to ~10⁻⁶ mA. Our study of ion migration reveals that ion migration is pronounced in organic–inorganic perovskite films but is suppressed in CsPbI₃, particularly in CsPbI₃ mixed with PCBM additive. This study shows that ion migration suppression by the exclusion of organic halide and the incorporation of PCBM additive can benefit low dark current in perovskite phototransistors. Full article

As derivatives of metal halide perovskite materials, low-dimensional metal halide materials have become important materials that have attracted much attention in recent years. As one branch, zinc-based metal halides have the potential for practical applications due to their lead-free, low-toxicity and high-stability characteristics. However, pure zinc-based metal halide materials are still limited by their poor optical properties and cannot achieve large-scale practical applications. Therefore, in this work, we report an organic–inorganic hybrid zero-dimensional zinc bromide, (TDMP)ZnBr₄, using transition metal Mn²⁺ ions as dopants and incorporating them into the (TDMP)ZnBr₄ lattice. The original non-emissive (TDMP)ZnBr₄ exhibits bright green emission under the excitation of external UV light after the introduction of Mn²⁺ ions with a PL peak position located at 538 nm and a PLQY of up to 91.2%. Through the characterization of relevant photophysical properties and the results of theoretical calculations, we confirm that this green emission in Mn²⁺:(TDMP)ZnBr₄ originates from the ⁴T₁ → ⁶A₁ optical transition process of Mn²⁺ ions in the lattice structure, and the near-unity PLQY benefits from highly localized electrons generated by the unique zero-dimensional structure of the host material (TDMP)ZnBr₄. This work provides theoretical guidance and reference for expanding the family of zinc-based metal halide materials and improving and controlling their optical properties through ion doping. Full article

Metal halide perovskites have shown excellent optoelectronic properties, including high photoluminescence quantum yield, tunable emission wavelengths, narrow full-width at half-maximums and a low-cost, solution-processed fabrication, which make it exhibit great potential as emission-layer materials of light-emitting diodes. With the joint efforts of researchers from different disciplines, there has been a significant progress in the improvement in the external quantum efficiency (EQE) and stability of perovskite light-emitting diodes (PeLEDs) in recent years, especially in green PeLEDs with EQEs over 30%. However, their operational stability lags behind other commercial organic and chalcogenide quantum dot emitters, limiting their practical application. In this review, we first introduce the basic device structure of PeLEDs, as well as the factors influencing the EQE and stability of PeLEDs. Secondly, the development of lead-based and lead-free PeLEDs are summarized systematically. Thirdly, challenges of PeLEDs are discussed in detail, including low the EQE of blue PeLEDs, poor device stability and EQE roll-off. Finally, some suggestions and perspectives for future research directions for PeLEDs are proposed. Full article

Heterogeneous photocatalysts incorporating metal halide perovskites (MHPs) have garnered significant attention due to their remarkable attributes: strong visible-light absorption, tuneable band energy levels, rapid charge transfer, and defect tolerance. Additionally, the promising optical and electronic properties of MHP nanocrystals can be harnessed for photocatalytic applications through controlled crystal structure engineering, involving composition tuning via metal ion and halide ion variations, dimensional tuning, and surface chemistry modifications. Combination of perovskites with other materials can improve the photoinduced charge separation and charge transfer, building heterostructures with different band alignments, such as type-II, Z-scheme, and Schottky heterojunctions, which can fine-tune redox potentials of the perovskite for photocatalytic organic reactions. This review delves into the activation of organic molecules through charge and energy transfer mechanisms. The review further investigates the impact of crystal engineering on photocatalytic activity, spanning a diverse array of organic transformations, such as C–X bond formation (X = C, N, and O), [2 + 2] and [4 + 2] cycloadditions, substrate isomerization, and asymmetric catalysis. This study provides insights to propel the advancement of metal halide perovskite-based photocatalysts, thereby fostering innovation in organic chemical transformations. Full article

Organometal halide perovskites have achieved great success in solution-processed photovoltaics. The explorations quickly expanded into other optoelectronic applications, including light-emitting diodes, lasers, and photodetectors. An in-depth analysis of the special scale effects is essential to understand the working mechanisms of devices and optimize the materials towards an enhanced performance. Generally speaking, organometal halide perovskites can be classified in two ways. By controlling the morphological dimensionality, 2D perovskite nanoplatelets, 1D perovskite nanowires, and 0D perovskite quantum dots have been studied. Using appropriate organic and inorganic components, low-dimensional organic–inorganic metal halide hybrids with 2D, quasi-2D, 1D, and 0D structures at the molecular level have been developed and studied. This provides opportunities to investigate the scale-dependent properties. Here, we present the progress on the characteristics of scale effects in organometal halide perovskites in these two classifications, with a focus on carrier diffusion, excitonic features, and defect properties. Full article

Organic–inorganic metal halide perovskite (OIMHP) has emerged as a promising material for solar cell application due to their outstanding optoelectronics properties. The perovskite-based solar cell (PSC) demonstrates a significant enhancement in efficiency of more than 20%, with a certified efficiency rating of 23.13%. Considering both the Shockley limit and bandgap, there exists a substantial potential for further efficiency improvement. However, stability remains a significant obstacle in the commercialization of these devices. Compared to organic carrier transport layers (CTLs), inorganic material such as ZnO, TiO₂, SnO₂, and NiO_X offer the advantage of being deposited using atomic layer deposition (ALD), which in turn improves the efficiency and stability of the device. In this study, methylammonium lead iodide (MAPbI₃)-based cells with inorganic CTL layers of SnO₂ and NiO_X are simulated using SCAPS-1D software. The cell structure configuration comprises ITO/SnO₂/CH₃NH₃PbI₃/NiO_X/Back contact where SnO₂ and NiO_X act as ETL and HTL, respectively, while ITO is a transparent front-end electrode. Detailed investigation is carried out into the influence of various factors, including MAPbI₃ layer size, the thickness of CTLs, operating temperature parasitic resistance, light intensity, bulk defects, and interfacial defects on the performance parameters. We found that the defects in layers and interface junctions greatly influence the performance parameter of the cell, which is eliminated through an ALD deposition approach. The optimum size of the MAPbI₃ layer and CTL was found to be 400 nm and 50 nm, respectively. At the optimized configuration, the PSC demonstrates an efficiency of 22.13%, short circuit current (JSC) of 20.93 mA/m², open circuit voltage (V_OC) of 1.32 V, and fill factor (FF) of 70.86%. Full article

In recent years, all-inorganic cesium lead halide perovskite quantum dots have emerged as promising candidates for various optoelectronic applications, including sensors, light-emitting diodes, and solar cells, owing to their exceptional photoelectric properties. However, their commercial utilization has been limited by stability issues. In this study, we addressed this challenge by passivating the surface defects of CsPbBr₃ quantum dots using indium acetate, a metal–organic compound. The resulting CsPbBr₃ quantum dots exhibited not only high photoluminescence intensity, but also a remarkably narrow half-peak width of 19 nm. Furthermore, by embedding the CsPbBr₃ quantum dots in ethylene-vinyl acetate, we achieved stretchability and significantly enhanced stability while preserving the original luminous intensity. The resulting composite film demonstrated the potential to improve the power conversion efficiency of crystalline silicon solar cells and enabled the creation of excellent white light-emitting diodes with coordinates of (0.33, 0.31). This co-passivation strategy, involving surface passivation and polymer packaging, provides a new idea for the practical application of CsPbBr₃ quantum dots. Full article