Search Results (66)

We report an advanced passivation strategy for perovskite solar cells (PSCs) by introducing core–shell structured perovskite quantum dots (PQDs), composed of methylammonium lead bromide (MAPbBr₃) cores and tetraoctylammonium lead bromide (tetra-OAPbBr₃) shells, during the antisolvent-assisted crystallization step. The epitaxial compatibility between the PQDs and the host perovskite matrix enables effective passivation of grain boundaries and surface defects, thereby suppressing non-radiative recombination and facilitating more efficient charge transport. At an optimal PQD concentration of 15 mg/mL, the modified PSCs demonstrated a remarkable increase in power conversion efficiency (PCE) from 19.2% to 22.85%. This enhancement is accompanied by improved device metrics, including a rise in open-circuit voltage (Voc) from 1.120 V to 1.137 V, short-circuit current density (Jsc) from 24.5 mA/cm² to 26.1 mA/cm², and fill factor (FF) from 70.1% to 77%. Spectral response analysis via incident photon-to-current efficiency (IPCE) revealed enhanced photoresponse in the 400–750 nm wavelength range. Additionally, long-term stability assessments showed that PQD-passivated devices retained more than 92% of their initial PCE after 900 h under ambient conditions, outperforming control devices which retained ~80%. These findings underscore the potential of in situ integrated PQDs as a scalable and effective passivation strategy for next-generation high-efficiency and stable perovskite photovoltaics. Full article

This work derived the relationship between the concentrations of Pb²⁺ and I⁻ vacancies, along with MA⁺ vacancies, in MAPbI₃ crystals and their effect on the short-circuit current of MAPbI₃-based solar photovoltaic devices. First principles calculations revealed that Pb²⁺ and I⁻ vacancies introduce shallow defect levels near the Fermi level, acting as non-radiative recombination centers, which significantly influence the short-circuit current and open-circuit voltage. In contrast, MA⁺ vacancies have a negligible effect on the optoelectronic properties of MAPbI₃. Based on this correlation, we successfully elucidated the declining trend of the short-circuit current (J_sc) in MAPbI₃-based devices with increasing Pb²⁺/I⁻ vacancy concentrations, while uncovering the microscopic mechanism responsible for the minor performance impact of MA⁺ vacancies. Full article

Metal halide perovskite (MHP) nanocrystals (NCs) offer great potential for high-efficiency optoelectronic devices; however, they suffer from structural softness and chemical instability. Doping MHP NCs can overcome this issue. In this work, we synthesize Mn-doped methylammonium lead bromide (MAPbBr₃) NCs using the ligand-assisted reprecipitation method and investigate their structural and optical stability. X-ray diffraction confirms Mn²⁺ substitution at Pb²⁺ sites and lattice contraction. Photoluminescence (PL) measurements show a blue shift, significant PL quantum yield enhancement, reaching 72% at 17% Mn²⁺ doping, and a 34% increase compared to undoped samples, attributed to effective defect passivation and reduced non-radiative recombination, supported by time-resolved PL data. Mn²⁺ doping also improves long-term stability under ambient conditions. Low-temperature PL reveals the crystal-phase transitions of perovskite NCs and Mn-doped NCs to be somewhat different than those of pure MAPbBr₃. Mn²⁺ incorporation into perovskite promotes self-assembly into superlattices with larger crystal sizes, better structural order, and stronger inter-NC coupling. These results demonstrate that Mn²⁺ doping enhances both optical performance and structural robustness, advancing the potential of MAPbBr₃ NCs for stable optoelectronic applications. Full article

Three-dimensional (3D) hybrid organic–inorganic perovskites (HOIPs) have attracted tremendous interest due to strong excitonic effects and large optical nonlinearities. Taking the advantages, 3D HOIPs show great potential for applications in excitonic and nonlinear devices. However, understanding the relevant mechanisms of exciton-associated nonlinear optical phenomena in 3D perovskites is still challenging. Here, we apply the quantum perturbation theory to calculate the exciton-associated degenerate 2PA spectra of 3D HOIPs. The calculated 2PA spectra of twelve 3D HOIPs are predicted to exhibit resonance peaks at both the sub-band and band edges. The exciton-resonance-associated 2PA coefficients are at least one order of magnitude larger than those of band-to-band transitions and are comparable to those of low-dimensional perovskites. To validate our model, we carried out measurements of the static light-intensity-dependent transmission on MAPbBr₃ single crystals. Enhancements of 2PA coefficients are predicted theoretically and observed experimentally with a resonant peak at 1100 nm, indicating intrinsic two-photon transitions to excitonic states in MAPbBr₃ single crystals. Full article

Fabrication and characterization based on experimental results for methylammonium lead iodide (MAPbI₃) perovskite solar cells using chemical-substituted metal phthalocyanines (MPc) and naphthalocyanines (MNc) as hole-transport materials have been performed to improve conversion efficiency (η) and stability. The purpose of this study was to fabricate and characterize a MAPbI₃ perovskite solar cell using t-butyl MPc and MNc as a hole-transporting layer to improve the photovoltaic performance and stability of η. Photovoltaic characteristics, morphology, crystallinity, and electronic structures were characterized in perovskite solar cells using MPc and MNc. The photovoltaic performance of the perovskite solar cell using t-butyl nickel phthalocyanine (NiPc) reached the maximum value of η at 13.4%. Incorporation of NiPc passivated the surface morphology by increasing the crystal grain size and supporting the carrier diffusion while suppressing carrier recombination near the grain boundary in the perovskite layer. Simulation using a SCAPS-1D program predicted the photovoltaic characteristics of the perovskite solar cell using NiPc. The photovoltaic mechanism was discussed on the basis of an energy diagram of the perovskite solar cell. The insertion of NiPc optimized energy levels near the highest occupied molecular orbital of NiPc and the valence band state of MAPbI₃, supporting a charge transfer related to short-circuit current density and η. Full article

It is necessary to overcome the relatively low conductivity of ionic liquids (ILs) caused by steric hindrance effects to improve their ability to passivate defects and inhibit ion migration to boost the photovoltaic performance of perovskite solar cells (PSCs). Herein, we designed and prepared a kind of low-concentration 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF₄) diluted with propylene carbonate (PC) via an ultrasonic technique (PC/IL). The decrease in the decomposition temperature related to the IL part and the increase in the sublimation temperature related to the PC part facilitated the use of PC/IL to effectively delay the crystallization process and passivate the defects in multiple ways to obtain high-quality perovskite films. Moreover, the increased conductivity of PC/IL and the more matched band alignment accelerated electron transport and collection. Finally, the MAPbI₃- and CsMAFA-based PSCs achieved PCE values of 20.87% and 23.29%, respectively, and their stabilities were greatly improved. This work provides a promising approach to optimizing ILs to achieve multiple functions and boost the performance of PSCs. Full article

Perovskite can be used to prepare high-performance photodetectors due to its excellent optical properties. However, the detection range of perovskite photodetectors is mostly limited to the visible light range, restricting their further development and application. In recent years, combining perovskite with organic bulk heterojunctions to prepare photodetectors with broadband detection capability has proven to be an effective strategy. Through this approach, the response spectrum of the photodetector can be flexibly regulated, and organic compounds can improve the perovskite film quality by passivating defects and inhibit the penetration of water molecules in the air, thereby improving the device performance and stability. In this work, we propose and demonstrate the feasibility of combining MAPbI₃ perovskite with PTB7-Th:COTIC-4F to prepare high-performance photodetectors with wide spectral response characteristics. With the assistance of an organic bulk heterojunction, the defects of perovskite crystals are effectively passivated, and the detection spectrum of the device is successfully extended to about 1100 nm. As a result, the responsivity achieved is 0.58 A/W, 1.19 A/W, and 1.41 A/W under laser illumination of 532 nm, 808 nm, and 980 nm, with the power density of 5 μW/cm² at the bias voltage of −0.5 V, respectively, which is one of the best performances among vertical device structures of this type. Moreover, the stability of the final hybrid film has been greatly improved. This work provides a new approach to the preparation of high-performance and broadband perovskite photodetectors. Full article

Organic/inorganic hybrid perovskite materials, such as CH₃NH₃PbX₃ (X = I, Br), have attracted the attention of the scientific community due to their excellent properties such as a widely tunable bandgap, high optical absorption coefficient, excellent power conversion efficiency, etc. The exposure of perovskite solar cells and photovoltaic devices to heat can significantly degrade their performance. Therefore, elucidating their temperature-dependent optical properties is essential for performance optimization of perovskite solar cells. We synthesized CH₃NH₃PbBr₃ (MAPbBr₃) single crystals through the polymer-controlled nucleation route and investigated the optical properties and molecular structure evolution of them with temperature. Through temperature evolution photoluminescence (PL) spectroscopy, we found that the fluorescence intensity was greatly affected by increasing the temperature, with an asymmetric PL profile suggesting that more captured excitons undergo radiative complexation. The optical photographs showed that the color of MAPbBr₃ single crystals faded. Raman spectroscopy revealed that during the heating process, the structure of MAPbBr₃ was still preserved at 90 °C since all of the Raman bands were very clear. When the temperature increased to 120 °C, the Raman bands of the internal modes became very weak. On further heating, the inorganic framework on sample’s surface started to disintegrate above 210 °C. During the heating process, the PL spectra exhibited significant changes in spectral intensity, peak position and Full Width Half Maximum (FWHM). The PL spectral intensity decreased abruptly with increasing temperature. The peak position was blue shifted with increasing temperature, and the peak shape showed an obvious asymmetry. The FMWH of the PL spectra was gradually broadened with the increase in the temperature, and there was a sharp increase from 270 °C to 300 °C. These variations in the PL spectra with temperature indicate that the optical properties of MAPbBr₃ are greatly affected by temperature, which in turn affects the application of MAPbBr₃ in fields such as optical devices. These results may be instructive for the application of MAPbBr₃. Full article

Perovskite single crystals have garnered significant interest in photodetector applications due to their exceptional optoelectronic properties. The outstanding crystalline quality of these materials further enhances their potential for efficient charge transport, making them promising candidates for next-generation photodetector devices. This article reports the synthesis of methyl ammonium lead bromide (MAPbBr₃) perovskite single crystal (SC) via the inverse-temperature crystallization method. To further improve the performance of the photodetector, Zn-porphyrin (Zn-PP) was used as a passivating agent during the growth of SC. The optical characterization confirmed the enhancement of optical properties with Zn-PP passivation. On single-crystal surfaces, integrated photodetectors are fabricated, and their photodetection performances are evaluated. The results show that the single-crystalline photodetector passivated with 0.05% Zn-PP enhanced photodetection properties and rapid response speed. The photoelectric performance of the device, including its responsivity (R), external quantum efficiency (EQE), detective nature (D), and noise-equivalent power (NEP), showed an enhancement of the un-passivated devices. This development introduces a new potential to employ high-quality perovskite single-crystal-based devices for more advanced optoelectronics. Full article

Although perovskite has great potential in optoelectronic devices, the simultaneous satisfaction of material stability and high performance is still an issue that needs to be solved. Most perovskite optoelectronic devices use quantum dot spin coating or the gas-phase growth of perovskite thin films as the photoelectric conversion layer. Due to stability limitations, these materials often experience a significant decrease in photoelectric conversion efficiency when encountering liquid reagents. The self-assembled growth of hybrid perovskite crystals determines superior lattice ordering and stability. There are three types of ionic liquids—[Emim]BF4, EMIMNTF2, and HMITFSI—that can effectively enhance the X-ray photoelectric conversion performance of hybrid perovskite crystal CH₃NH₃PbI₃ (MAPbI₃), and the enhancement in the photocurrent leads to an improvement in the sensitivity of X-ray detectors. We soak the perovskite crystals in an ionic liquid and perform two treatment methods: electrification and dilution with ETOH solution. It is interesting to find that MAPbI₃ perovskite single crystal materials choose the same optimized ionic liquid species in X-ray detection and photovoltaic power generation applications, and the effect is quite the opposite. Compared with untreated MAPbI₃ crystals, the average photocurrent density of Electrify-HMITFSI MAPbI₃ increased by 826.85% under X-ray excitation and the sensitivity of X-ray detectors made from these treated MAPbI₃ crystals significantly increased by 72.6%, but the intensity of the PL spectrum decreased to 90% of the untreated intensity. Full article

Perovskite solar cells are attracting more and more attention due to their higher absorption and low cost. However, fabricating the perovskite film with high crystallinity and ideal morphology, which presents large-size and uniform particles with fewer grain boundaries, still needs further improvement. Herein, we introduce MAPbCl₃ crystals into the PbI₂ film in the sequential deposition process, which obtained the controlled crystallization in perovskite films. The perovskite films induced by MAPbCl₃ have stronger crystallinity, fewer defect states, and larger grain size, reducing carrier recombination and improving carrier transfer. The optimized perovskite solar cell (PSC) has achieved a power conversion efficiency of 20.97%. Furthermore, the stability of PSCs has also been enhanced due to the reduced grain boundaries impeding moisture diffusion. This strategy can be applied in other solution-based fabrication processes to improve the photovoltaic performance of PSCs. Full article

In recent years, there have been intense studies on hybrid organic–inorganic compounds (HOIPs) due to their tunable and adaptable features. This present study reports the vibrational, structural, and elastic properties of mixed halide single crystals of MA_xFA_1-xPbCl₃ at room temperature by introducing the FA cation at the A-site of the perovskite crystal structure. Powder X-ray diffraction analysis confirmed that its cubic crystal symmetry is similar to that of MAPbCl₃ and FAPbCl₃ with no secondary phases, indicating a successful synthesis of the MA_xFA_1-xPbCl₃ mixed halide single crystals. Structural analysis confirmed that the FA substitution increases the lattice constant with increasing FA concentration. Raman spectroscopy provided insight into the vibrational modes, revealing the successful incorporation of the FA cation into the system. Brillouin spectroscopy was used to investigate the changes in the elastic properties induced via the FA substitution. A monotonic decrease in the sound velocity and the elastic constant suggests that the incorporation of large FA cations causes distortion within the inorganic framework, altering bond lengths and angles and ultimately resulting in decreased elastic constants. An analysis of the absorption coefficient revealed lower attenuation coefficients as the FA content increased, indicating reduced damping effects and internal friction. The current findings can facilitate the fundamental understanding of mixed lead chloride perovskite materials and pave the way for future investigations to exploit the unique properties of mixed halide perovskites for advanced optoelectronic applications. Full article

We have fabricated planar interdigitated photodetectors exhibiting high responsivity. These detectors are based on thin layers of methylammonium lead bromide (MAPbBr₃) at 90 nm thickness. MAPbBr₃ thin films were first characterized on glass (borosilicate) substrates using absorption and photoluminescence measurements showing a high absorption edge at 521 nm and strong emission at 530 nm, as expected. MAPbBr₃ thin films were then deposited on top of interdigitated electrodes, hence producing planar photodetectors with responsivity up to 0.4 A/W. Such higher performances were attributed to the interdigitated design, low crack density (0.05 µm⁻²), and lower resistivity (20 MΩ.cm) compared to MAPbBr₃ single crystal. Therefore, this work highlights MAPbBr₃ thin films as very promising for photodetection applications. Full article

The synergistic combination of hybrid perovskites with graphene-related materials is leading to optoelectronic devices with enhanced performance and stability. Still, taking advantage of the solution processing of perovskite onto graphene is especially challenging. Here, MAPbBr₃ perovskite is grown on single-layer graphene/graphene oxide (Gr/GO) patterns with 120 µm periodicity using a solution-processed method. MAPbBr₃ rounded crystals are formed with sizes ranging from nanometers to microns, either forming continuous films or dispersed particles. A detailed morphological and structural study reveals a fully oriented perovskite and very different growth habits on the Gr/GO micro-patterns, which we relate to the substrate characteristics and the nucleation rate. A simple method for controlling the nucleation rate is proposed based on the concentration of the precursor solution and the number of deposited perovskite layers. The photoluminescence is analyzed in terms of the crystal size, strain, and structural changes observed. Notably, the growth on top of Gr/GO leads to a huge photostability of the MAPbBr₃ compared with that on glass. Especially outstanding is that of the microcrystals, which endure light densities as high as 130 kW/cm². These results allow for anticipating the design of integrated nanostructures and nanoengineered devices by growing high-stability perovskite directly on Gr/GO substrates. Full article

Organic inorganic perovskite materials have received increasing attention in the optoelectronic field because of their unique properties. The ultrafast dynamics of photogenerated carriers determine photoelectric conversion efficiency, thus, it is feasible to influence the dynamics behavior of photogenerated carriers by regulating A-site cations. This paper mainly used transient absorption spectra (TAS) technology to study the photogenerated carriers relaxation processes of organic–inorganic perovskite Cs_xMA_1−xPbI₃ materials at different x values. Three sets of time constants were obtained by global fitting at different values of x. The experimental results showed that the crystal structure of perovskite could be affected by adjusting the Cs⁺ doping amount, thereby regulating the carrier dynamics. The appropriate amount of A-cation doping not only maintained the organic–inorganic perovskite crystal phase, but also prolonged the photogenerated carrier’s lifetime. The 10% Cs⁺ doping Cs_xMA_1−xPbI₃ perovskite has potential for solar cell applications. We hope that our research can provide dynamics support for the development of organic–inorganic perovskite in solar cells. Full article