Hybrid Organic-inorganic Lead Halide Perovskites Research Articles

Insights from Theoretical Modeling of Cesium-Formamidinium-Based Mixed-Halide Perovskite Solar Cells for Outdoor and Indoor Applications.

This study presents an in-depth computational analysis of hybrid organic-inorganic lead halide perovskite solar cells (PSCs) with a composition of Cs0.17FA0.83Pb(Br0.4I0.6)3 (FA: formamidinium) material under cool and warm light-emitting diodes (LEDs). We propose a novel design of an inverted (p-i-n) PSC to compare the power conversion efficiencies (PCEs) of opaque and semitransparent models under the AM1.5G spectrum and indoor LED lighting. The Shockley-Queisser (SQ) limits were estimated for LEDs with color temperatures of 3000 and 6000 K, revealing significant differences in PCE compared to standard solar radiation. The optical and electrical properties of the perovskite devices were simulated by using the transfer-matrix method and one-dimensional drift-diffusion model. We report a PCE of 15.8% for opaque devices under the AM1.5G spectrum, while the semitransparent devices exhibit PCEs of 12.07% and 10.17% for front and rear illumination, respectively. Under indoor conditions with cool LED lighting, the opaque devices demonstrate a significantly higher PCE of 28.38% and an impressive photovoltage of 1.17 V, surpassing the semitransparent devices, which show efficiencies of approximately 19.5% (front illumination) and 18.3% (rear illumination). While the interface between the hole transport layer and perovskite has a major impact on the device performance of opaque solar cells, the perovskite/electron transport layer junction plays a more critical role in the performance of semitransparent solar cells. The power densities for opaque devices reached up to 106.25 μW/cm2 under cool LED and 97.1 μW/cm2 with warm LED illumination. For semitransparent devices, the power densities exceeded 60.71 μW/cm2 on front-side illumination and 73.66 μW/cm2 on rear illumination under cool LEDs. These results emphasize the significant potential of hybrid PSCs for efficient energy harvesting under various lighting conditions, making them promising candidates for powering low-energy-consumption electronics in indoor environments.

Progress of Hole-Transport Layers in Mixed Sn-Pb Perovskite Solar Cells.

Hybrid organic-inorganic lead halide perovskite solar cells (PSCs) have rapidly emerged as a promising photovoltaic technology, with record efficiencies surpassing 26%, approaching the theoretical Shockley-Queisser limit. The advent of all-perovskite tandem solar cells (APTSCs), integrating Pb-based wide-bandgap (WBG) with mixed Sn-Pb narrow-bandgap (NBG) perovskites, presents a compelling pathway to surpass this limit. Despite recent innovations in hole transport layers (HTLs) that have significantly improved the efficiency and stability of lead-based PSCs, an effective HTL tailored for Sn-Pb NBG PSCs remains an unmet need. This review highlights the essential role of HTLs in enhancing the performance of Sn-Pb PSCs, focusing on their ability to mitigate non-radiative recombination and optimize the buried interface, thereby improving film quality. The distinct attributes of Sn-Pb perovskites, such as their lower energy levels and accelerated crystallization rates, necessitate HTLs with specialized properties. In this study, the latest advancements in HTLs are systematically examined for Sn-Pb PSCs, encompassing organic, self-assembled monolayer (SAM), inorganic materials, and HTL-free designs. The review critically assesses the inherent limitations of each HTL category, and finally proposes strategies to surmount these obstacles to reach higher device performance.

Lead-free Cs3Bi2I9 perovskite hexagonal microplates: A promising material solution-processed for ultraviolet self-powered photodetectors

In recent times, hybrid organic-inorganic lead halide perovskites have garnered significant attention in the realm of optoelectronic devices. Metal halide perovskites are extensively researched for photodetection due to their exceptional optical and electrical properties. However, the toxicity of lead and the unstable nature of organic components are limiting its potential. Lead-free perovskites, on the other hand, have low toxicity and are being explored as a promising material for photodetector applications. However, achieving self-powered perovskite photodetectors with high photoresponse, broad spectral sensitivity, and long-term stability remains challenging Among them, Cs3Bi2I9 perovskites have emerged as standout, garnering attention for their environmentally friendly nature, impressive stability, and heightened photosensitivity. Herein, FTO/ Al-doped ZnO (AZO)/Cs3Bi2I9/P3HT/C self-powered ultra-violet (UV) photodetector. This device demonstrated outstanding self-powered photodetection capabilities with a photoresponsivity of 29 mA/W, a specific detectivity of 1.05×1011 Jones, and an impressive response rise and decay time of 90 ms /140 ms. Furthermore, the PDs device can function as a bias-based UV photodetector.

Chitosan Mediated FAPbBr3 Nanocrystal Thin‐Films with High Color Purity and Enhanced Hole Mobility

Composite materials which combine the advantages of both embedded constituents have been a successful strategy for developing novel multi‐functional materials. Here, we demonstrate the synthesis of nanoscale materials of organic‐inorganic hybrid lead halide perovskites (OIH‐LHP) with enhanced optoelectronic properties and photostability by utilizing biomimetic ligand, chitosan. Notably, nanocrystals fabricated with chitosan mediated ligands exhibit an increase in photoluminescence quantum yield by 300% and fluorescence lifetime by 1.5 times. Consequently, the lifetime distribution of the photoluminescence emission decreases to a value as low as 6 ns. More interestingly, even though chitosan is a wide band gap insulating material, its incorporation onto the perovskite NCs enhances the bulk hole mobility by at least an order of magnitude in comparison to the pristine material. With detailed spectroscopic and structural studies, we correlate these enhancements in optoelectronic parameters to the improvement in the crystal quality, phase purity, and minimized poly‐dispersity of the nanocrystals. Development of such composite materials with unprecedented optoelectronic properties and outstanding stability will contribute immensely towards high performance nanocrystal devices.

The Effect of Cesium Incorporation on the Vibrational and Elastic Properties of Methylammonium Lead Chloride Perovskite Single Crystals.

Hybrid organic-inorganic lead halide perovskites (LHPs) have emerged as a highly significant class of materials due to their tunable and adaptable properties, which make them suitable for a wide range of applications. One of the strategies for tuning and optimizing LHP-based devices is the substitution of cations and/or anions in LHPs. The impact of Cs substitution at the A site on the structural, vibrational, and elastic properties of MAxCs1-xPbCl3-mixed single crystals was investigated using X-ray diffraction (XRD) and Raman and Brillouin light scattering techniques. The XRD results confirmed the successful synthesis of impurity-free single crystals, which exhibited a phase coexistence of dominant cubic and minor orthorhombic symmetries. Raman spectroscopy was used to analyze the vibrational modes associated with the PbCl6 octahedra and the A-site cation movements, thereby revealing the influence of cesium incorporation on the lattice dynamics. Brillouin spectroscopy was employed to investigate the changes in elastic properties resulting from the Cs substitution. The incorporation of Cs cations induced lattice distortions within the inorganic framework, disrupting the hydrogen bonding between the MA cations and PbCl6 octahedra, which in turn affected the elastic constants and the sound velocities. The substitution of the MA cations with smaller Cs cations resulted in a stiffer lattice structure, with the two elastic constants increasing up to a Cs content of 30%. The current findings facilitate a fundamental understanding of mixed lead chloride perovskite materials, providing valuable insights into their structural and vibrational properties.

Trace organic–inorganic hybrid lead halide perovskite nanocrystals as photocatalysts for PET-RAFT polymerization with high efficiency

Lead halide perovskite has emerged as a new class of materials in photocatalysis due to its promising photocatalytic performance. Here, we introduce organic–inorganic hybrid lead halide perovskite (OIHP) nanocrystals as photocatalysts (PCs) for efficient photoinduced electron/energy transfer–reversible addition–fragmentation chain transfer (PET-RAFT) polymerization. PET-RAFT polymerization is successfully conducted with 0.025 wt% PC loading under blue light (6 mW/cm2, 460 nm), yielding upwards of 90 % monomer conversion and polymer products with narrow dispersity (≤1.20) within 2 h, demonstrating a fast polymerization rate. Moreover, the oxygen resistance of the polymerization process has been demonstrated. Due to the advantages of low PC usage, fast polymerization rate and oxygen tolerance, OIHP mediated PET-RAFT polymerization is expected to be used for large-scale production and industrial applications.

Solution Processed Hybrid Lead Perovskite Films for White Light Emission and Lasing Applications

Abstract2D organic–inorganic hybrid lead halide perovskite films are fascinating optoelectronic materials for white‐light emission and lasing applications. Here, it is demonstrated that nano‐meter‐thick films of perovskites can be formed at room temperature using Langmuir–Schaefer (LS) deposition technique. In situ X‐ray measurements reveal a self‐assembly process of the 2D perovskite formation at the air–water interface. This formation process requires the presence of stearic acid monolayer on the water subphase having a solution of lead‐perovskite in dimethylformamide. Microscopy and X‐ray measurements of these nanofilms transferred onto substrates show crystalline phase formation that deviates from the known orthorhombic structure of the bulk crystals. The nanofilms exhibit novel broad optical emission with sharp band‐edge transition in temperature‐dependent photoluminescence studies. Also, their band‐edge emission is distinctly blue‐shifted compared to that of thicker 2D perovskite flakes prepared by the slow‐cooling chemical synthesis process. 2D flakes exhibit lasing that cannot be obtained in the LS nanofilms as their thicknesses are lower than the lasing wavelength prohibiting wave‐guide formation. The results show that the 2D single‐crystalline nature of the LS films and flakes are suitable materials to develop broad‐band white light emission across the entire visible range and to obtain lasing without external cavities, respectively.

Coherent Carrier Spin Dynamics in FAPbBr3 Perovskite Crystals.

Coherent spin dynamics of electrons and holes are studied in hybrid organic-inorganic lead halide perovskite FAPbBr3 bulk single crystals using the time-resolved Kerr ellipticity technique at cryogenic temperatures. The Larmor spin precession of the carrier spins in a magnetic field is monitored to measure the Landé g-factors of electrons (+2.44) and holes (+0.41). These g-factors are highly isotropic. The measured spin dephasing times amount to a few nanoseconds, and the longitudinal hole spin relaxation time is 470 ns. The important role of the strong hyperfine interaction between carrier spins and nuclear spins is demonstrated via dynamic nuclear polarization. At low temperatures, electron and hole spin relaxation predominantly occurs via the hyperfine interaction, whose importance significantly decreases at temperatures above 12 K. We overview the spin dynamics in various lead halide perovskite crystals and polycrystalline films and conclude on their common features provided by charge carrier localization at cryogenic temperatures.

Compositional Engineering of Hybrid Organic-Inorganic Lead-Halide Perovskite and PVDF-Graphene for High-Performance Triboelectric Nanogenerators.

Triboelectric nanogenerators (TENGs) have attracted a great deal of attention since they can convert ubiquitous mechanical energy into electrical energy and serve as a continuous power source for self-powered sensors. Optimization of the dielectric material composition is an effective way to improve the triboelectric output performance of TENGs. Herein, the hybrid organic-inorganic lead-iodide perovskite Cs0.05FA0.95-xMAxPbI3 was prepared by blade coating and used as a positive friction layer material. Moreover, PVDF-graphene (PG) nanofibers were prepared as negative friction layer materials by electrostatic spinning. The output performance of the TENG was enhanced by varying the MA content of the pervoskite films and the graphene content of the PG nanofibers. The champion output TENG based on Cs0.05FA0.9MA0.05PbI3/PG-0.15 achieved an open-circuit voltage of 245 V, a short-circuit current of 24 μA, and a charge transfer of 80.2 nC. Meanwhile, a maximum power density of 11.23 W m-2 was obtained at 100 MΩ. Moreover, the device exhibits excellent energy-harvesting properties, including excellent stability and durability, rapidly charges capacitors, and lights commercial LEDs and digital tubes.

Broadband blue light emissions of one-dimensional hybrid Cu(I) halides with ultrahigh anti -water stability.

Low-dimensional organic-inorganic hybrid lead halide perovskites have attracted much interest in solid-state lighting and displays, but the toxicity and instability of lead halide are obstacles to their industrial applications, which must be overcome. As an alternative, Cu(I)-based hybrid metal halides have emerged as a new type of luminescent material owing to their diversified structure, adjustable luminescence, low toxicity and low cost. Herein, we report three one-dimensional (1D) hybrid Cu(I)-based halides with the general formula ACu2Br4 (A = [(Me)4-Pipz]2+ and [BuDA]2+ and [TMEDA]2+). These 1D hybrid Cu(I) halides display stable broadband blue emission with maximum emission peaks in the range of 445-474 nm and the highest photoluminescence quantum yield of 37.8%. Furthermore, in-depth experimental and theoretical investigations revealed that the broadband blue emissions originate from the radiative recombination of self-trapped excitons. Most importantly, there is no structural degradation and attenuation of emission intensity even after continuously soaking these halides in water for at least two months, demonstrating their ultra-high anti-water stability. Hirshfeld surface analysis shows that a large number of weak hydrogen bonds can protect the inorganic skeleton from degradation due to water. This work provides a new strategy for the design of water-stable Cu(I)-based halides with efficient blue emission and wide potential applications in humid environments.

Phase Transitions, Dielectric Response, and Nonlinear Optical Properties of Aziridinium Lead Halide Perovskites.

Hybrid organic-inorganic lead halide perovskites are promising candidates for next-generation solar cells, light-emitting diodes, photodetectors, and lasers. The structural, dynamic, and phase-transition properties play a key role in the performance of these materials. In this work, we use a multitechnique experimental (thermal, X-ray diffraction, Raman scattering, dielectric, nonlinear optical) and theoretical (machine-learning force field) approach to map the phase diagrams and obtain information on molecular dynamics and mechanism of the structural phase transitions in novel 3D AZRPbX3 perovskites (AZR = aziridinium; X = Cl, Br, I). Our work reveals that all perovskites undergo order-disorder phase transitions at low temperatures, which significantly affect the structural, dielectric, phonon, and nonlinear optical properties of these compounds. The desirable cubic phases of AZRPbX3 remain stable at lower temperatures (132, 145, and 162 K for I, Br, and Cl) compared to the methylammonium and formamidinium analogues. Similar to other 3D-connected hybrid perovskites, the dielectric response reveals a rather high dielectric permittivity, an important feature for defect tolerance. We further show that AZRPbBr3 and AZRPbI3 exhibit strong nonlinear optical absorption. The high two-photon brightness of AZRPbI3 emission stands out among lead perovskites emitting in the near-infrared region.

Optical and structural characterization of CsPb(I1-xBrx)3 nanomaterials prepared by the mechanochemical method

Hybrid organic-inorganic lead halide perovskites (LHP) are gaining considerable attention due to their wide range of potential applications, particularly as an active layer in solar cells and light-emitting devices owing to their excellent light-harvesting and photoluminescence emission properties. Considering their high color purity and color-tunability, high photoluminescence quantum yield (PLQY), easy fabrication, and cost-efficiency, LHP are promising candidates to compete with the traditional active layer in solid-state lighting. The PL emission of CsPbX3 (X = I, Br, Cl) covers the entire visible range from 400 to 730 nm and can be easily tuned via halide replacement in the I ↔ Br ↔ Cl series. In this work, photoluminescence (PL), luminescence excitation, UV/VIS/NIR absorption, structural and morphological properties of CsPb(I1-xBrx)3 (x = 0–1) nanosized powders prepared by the mechanochemical synthesis method is investigated at 80K and room temperature. A narrow PL peak with full width at half maximum (FWHM) = 16.5 and 6.6 nm was observed at room temperature and 80K from CsPbBr3, respectively. The relation between structure and optical properties of nanopowders is discussed. It is shown that the halide exchange mechanism is an effective approach for fabrication of defect-free materials.

Tailoring Interlayer Charge Transfer Dynamics in 2D Perovskites with Electroactive Spacer Molecules.

The family of hybrid organic-inorganic lead-halide perovskites are the subject of intense interest for optoelectronic applications, from light-emitting diodes to photovoltaics to X-ray detectors. Due to the inert nature of most organic molecules, the inorganic sublattice generally dominates the electronic structure and therefore the optoelectronic properties of perovskites. Here, we use optically and electronically active carbazole-based Cz-Ci molecules, where Ci indicates an alkylammonium chain and i indicates the number of CH2 units in the chain, varying from 3 to 5, as cations in the two-dimensional (2D) perovskite structure. By investigating the photophysics and charge transport characteristics of (Cz-Ci)2PbI4, we demonstrate a tunable electronic coupling between the inorganic lead-halide and organic layers. The strongest interlayer electronic coupling was found for (Cz-C3)2PbI4, where photothermal deflection spectroscopy results remarkably reveal an organic-inorganic charge transfer state. Ultrafast transient absorption spectroscopy measurements demonstrate ultrafast hole transfer from the photoexcited lead-halide layer to the Cz-Ci molecules, the efficiency of which increases by varying the chain length from i = 5 to i = 3. The charge transfer results in long-lived carriers (10-100 ns) and quenched emission, in stark contrast to the fast (sub-ns) and efficient radiative decay of bound excitons in the more conventional 2D perovskite (PEA)2PbI4, in which phenylethylammonium (PEA) acts as an inert spacer. Electrical charge transport measurements further support enhanced interlayer coupling, showing increased out-of-plane carrier mobility from i = 5 to i = 3. This study paves the way for the rational design of 2D perovskites with combined inorganic-organic electronic properties through the wide range of functionalities available in the world of organics.

Introducing Ferroelasticity into 1D Hybrid Lead Halide Semiconductor by Halogen Substitution Strategy.

Organic-inorganic hybrid lead halide perovskites (OLHPs), represented by (CH3 NH3 )PbI3 , are one of the research focus due to their exceptional performance in optoelectronic applications, and ferroelastic domain walls are benign to their charge carrier transport that is confirmed recently. Among them, the 1DOLHPs feature better stability against desorption and moisture, but related 1D ones possessing ferroelasticity are rarely investigated and reported so far. In this work, the 1D ferroelastic semiconductor (N-iodomethyl-N-methyl-morpholinium)PbI3 ((IDMML)PbI3 ) is prepared successfully by introducing successively halogenate atoms from Cl, Br to I into the organic cation of the prototype (N,N-dimethylmorpholinium)PbI3 ((DMML)PbI3 ). Notably, (IDMML)PbI3 shows the narrow bandgap energy (≈2.34eV) according to the ultraviolet-visible absorption spectrum and the theoretical calculation, and possesses the evident photoconductive characteristic with the on/off ratio of current of ≈50 under the 405nm light irradiation. This work provides a new case for the ferroelastic OLHPs and will inspire intriguing research in the field of optoelectronic.

Long-Lived Exciton Coherence in Mixed-Halide Perovskite Crystals.

Compositional engineering of the optical properties of hybrid organic-inorganic lead halide perovskites is crucial for the realization of efficient solar cells and light-emitting devices. We study the effect of band gap fluctuations on coherent exciton dynamics in a mixed FA0.9Cs0.1PbI2.8Br0.2 perovskite crystal by using photon echo spectroscopy. We reveal a narrow homogeneous exciton line width of 16 μeV at a temperature of 1.5 K. The corresponding exciton coherence time T2 = 83 ps is exceptionally long due to the localization of excitons at the scale of tens to hundreds of nanometers. From spectral and temperature dependences of the two- and three-pulse photon echo decay, we conclude that for low-energy excitons pure decoherence associated with elastic scattering on phonons is comparable with the exciton lifetime, while for excitons with higher energies, inelastic scattering to lower energy states via phonon emission dominates.

A Data-Driven Platform for Two-Dimensional Hybrid Lead-Halide Perovskites.

The exceptional properties of two-dimensional hybrid organic-inorganic lead-halide perovskites (2D HOIPs) have led to a rapid increase in the number of low-dimensional materials for optoelectronic engineering and solar energy conversion. The flexibility and controllability of 2D HOIPs create a vast structural space, which presents an urgent issue to effectively explore 2D HOIPs with better performance for practical applications. However, the traditional RP-DJ classification method falls short in describing the influence of structure on the electronic properties of 2D HOIPs. To overcome this limitation, we employed inorganic structure factors (SF) as a classification descriptor, which considers the influence of inorganic layer distortion of 2D HOIPs. And we investigated the relationship between SF, other physicochemical features, and band gaps of 2D HOIPs. By using this structural descriptor as a feature for a machine learning model, a database of 304920 2D HOIPs and their structural and electronic properties was generated. A large number of previously neglected 2D HOIPs were discovered. With the establishment of this database, experimental data and machine learning methods were combined to develop a 2D HOIPs exploration platform. This platform integrates searching, download, analysis, and online prediction, providing a useful tool for the further discovery of 2D HOIPs.

Minimal Molecular Building Blocks for Screening in Quasi-Two-Dimensional Organic-Inorganic Lead Halide Perovskites.

Layered hybrid organic-inorganic lead halide perovskites have intriguing optoelectronic properties, but some of the most interesting perovskite systems, such as defective, disordered, or mixed perovskites, require multiple unit cells to describe and are not accessible within state-of-the-art ab initio theoretical approaches for computing excited states. The principal bottleneck is the calculation of the dielectric matrix, which scales formally as O(N4). We develop here a fully ab initio approximation for the dielectric matrix, known as IPSA-2C, in which we separate the polarizability of the organic/inorganic layers into minimal building blocks, thus circumventing the undesirable power-law scaling. The IPSA-2C method reproduces the quasi-particle band structures and absorption spectra for a series of Ruddlesden-Popper perovskites to high accuracy, by including critical nonlocal effects neglected in simpler models, and sheds light on the complicated interplay of screening between the organic and inorganic sublattices.

High-performance photodetector based on semi-encompassed CH3NH3PbCl3–ZnO microwire heterojunction with alterable spectral response

Recently, heterojunctions consisting of hybrid organic-inorganic lead (Pb) halide perovskites and other semiconductors have drawn increasing attention for the potential application in photodetectors due to their exceptional performance. However, their performance is usually limited by the relatively low crystalline quality of perovskites, and the response spectra of the devices are difficult to adjust according to the practical requirement. Here, high quality CH3NH3PbCl3 micro-sized crystals have been successfully fabricated on one side of individual ZnO microwire to form heterojunction photodetector by a two-step crystallization method. The heterojunction device presents a low dark current (60 nA at −6 V) along with a rapid response speed (rise time of <20 μs and fall time of ∼500 μs). More interestingly, the modulation of the response spectra and the responsivity can be realized by operating the device under front or back illumination due to the self-filtering properties. Our findings provide a promising method for combining perovskites with other inorganic materials to form high-performance heterojunction photodetectors.

Investigation of thickness dependent efficiency of CsPbX3 (X = I, Br) absorber layer for perovskite solar cells

The drawbacks of solar cells consisting of hybrid organic-inorganic lead halide perovskites led to the development of solar cells containing completely inorganic perovskites. Therefore, here we have carried out detailed density functional theory (DFT) based investigation of cubic phase CsPbX3 (X = I, Br). Absence of imaginary frequencies in phonon dispersion curves and negative cohesive energies of the perovskites depicts stability of our crystal structures. From electronic properties of CsPbI3 and CsPbBr3 we have deduced that the major contributions in their valence band region is due to I-5p and Br-4p orbitals, respectively. The static dielectric constant of CsPbI3 is greater than CsPbBr3 which shows that it consists of low carrier recombination rate. Red shift has also been observed in absorption coefficient plot while going from Br → I in CsPbX3. The thickness of absorber layer present in perovskite solar cells (PSCs) directly influences its efficiency and stability. Therefore, here we have used a detailed framework i.e., spectroscopic limited maximum efficiency (SLME) to predict solar cell parameters of perovskites absorber layer as a function of their thicknesses. Using SLME approach which is thickness dependent it has been predicted that at thicknesses above 2.56 μm and 1.39 μm of absorber layers CsPbI3 and CsPbBr3, respectively, their efficiencies obtained using SLME approach are higher compared to that obtained using Shockley-Queisser (SQ) limit. The efficiencies of CsPbI3 and CsPbBr3 absorber layers calculated using SLME approach at absorber thickness of 20 μm are obtained around 30.41% and 24.53%, respectively.

Fabrication of two-dimensional hybrid organic–inorganic lead halide perovskites with controlled multilayer structures by liquid-phase laser ablation

We proposed a novel fabrication method of layered two-dimensional lead halide perovskites by liquid-phase laser ablation. Spacings between lead halide monolayer sheets can be controlled by choosing species of organic amine additives.