Search Results (83)

The use of LIDAR sensors is rapidly increasing across various fields, including autonomous transportation, robotics, security systems, and biosensing. Among the core components of LIDAR systems, short-wave infrared (SWIR) sensors play a crucial role in detecting infrared light reflected from objects to recognize the surrounding environment and humans. Various types of SWIR sensors have been reported, with growing demand for those capable of detecting eye-safe infrared wavelengths above 1400 nm. In particular, quantum dot (QD)-based SWIR sensors are attracting attention due to their tunable wavelength range within the eye-safe region, narrow full width at half maximum (FWHM), and selective detection with minimal interference from other infrared wavelengths. Moreover, QD-based SWIR photodetectors can be synthesized and fabricated via solution-based methods, offering advantages such as low cost and ease of fabrication. However, the long organic ligands typically present on QDs exhibit insulating properties, limiting the sensitivity and stability of the photodetectors. To address this issue, organic ligands can be replaced with short inorganic ligands possessing superior electrical conductivity. In this study, the organic ligands of synthesized PbS QDs were replaced with the inorganic ligand methylammonium lead iodide (MAPI) in solution, and a SWIR photodetector was fabricated. The MAPI-capped PbS QD-based photodetector exhibited remarkable external quantum efficiency (EQE) of 62%, a responsivity of 0.73 A/W, and a detectivity of 2.26 × 10¹¹ Jones within the 1400–1500 nm wavelength range. Full article

Flexible X-ray detectors have emerged as a promising technology for portable medical imaging and wearable electronics, yet their manufacturing remains constrained by the competing requirements of device performance, mechanical conformability, and production scalability. Conventional solution-based deposition methods fail to yield high-quality perovskite thick films with uniform morphology, while vacuum evaporation techniques are limited by exorbitant operational costs and low throughput. Herein, we report an optimized solution-processed vacuum evaporation strategy that enables the fabrication of high-quality perovskite films (~1 μm thick) on flexible polyethylene naphthalate (PEN) substrates at a low processing temperature of 100 °C. By incorporating tailored additives into the precursor solution and precisely modulating the vapor-phase conversion kinetics, we achieved significant improvements in film density, crystallinity, and morphological uniformity. Systematic investigations were conducted to elucidate the structure–property relationships across three material systems: pure methylammonium lead iodide (MAPbI₃), halogen-doped methylammonium lead iodide-bromide (MAPb(IBr)₃), and synergistic cation-halogen engineered cesium-methylammonium lead iodide-bromide (CsMAPb(IBr)₃). The optimized flexible PIN-type X-ray detector based on CsMAPb(IBr)₃ exhibited exceptional performance metrics, including a dark current density as low as 5.2 nA cm⁻² and an X-ray sensitivity of up to 1.43 × 10⁴ μC·Gy_air⁻¹·cm⁻². Remarkably, the device retained over 95% of its initial performance after 400 bending cycles with a bending radius of 6 mm, demonstrating outstanding mechanical robustness and operational durability. This work establishes a viable, cost-effective technical route for the scalable production of high-performance flexible X-ray detectors, addressing critical challenges in the advancement of next-generation portable imaging technologies. Full article

Self-powered perovskite photodiodes provide an attractive platform for low-power and high-sensitivity photodetection; however, their performance capabilities are often constrained by inefficient interfacial charge extraction and noise suppression. Here, we report a polymer-mediated interfacial engineering strategy for methylammonium lead iodide (MAPbI₃) photodiodes by integrating thermally optimized nickel oxide (NiO_x) hole-transport layers (HTLs) with a nonionic polymeric surfactant, poly(oxyethylene)(10) tridecyl ether (PTE). NiO_x films annealed at 300 °C establish a favorable energetic baseline for hole extraction, while the ppm-level incorporation of PTE into the MAPbI₃ precursor enables the molecular-scale modulation of the NiO_x/MAPbI₃ interface without forming an additional interlayer. The external quantum efficiency at 640 nm increases from 78.7% for pristine MAPbI₃ to 84.1% and 84.6% for devices incorporating 30 and 60 ppm PTE, corresponding to enhanced responsivities of 406, 434, and 437 mA/W. These improvements translate into reduced noise-equivalent power and an increase in the noise-limited detectivity from 2.50 × 10¹² to 2.76 × 10¹² Jones under zero-bias operation. Importantly, enhanced sensitivity is achieved without compromising the dynamic performance, as all devices retain fast temporal responses and kilohertz-level bandwidths. These results establish polymeric-surfactant-assisted interfacial engineering as a scalable and effective platform for low-noise, high-sensitivity self-powered perovskite photodiodes for renewable-energy-integrated systems. Full article

In this work, we report a protective encapsulation intended as the final coating layer on solar cells. The formulation consists of polylactic (PLA)-based resin, modified with hexadecyltrimethoxysilane (HDTMS), epoxidized polybutadiene (EPB), and benzotriazole as a UV absorber with approximate weight fractions ranging from 20 to 60 wt% for PLA, 30–80 wt% for solvents (toluene and chloroform), and 0–5 wt% for HDTM, EPB, and benzotriazole with percentages 54.2%, 29.2%, and 16.7%, respectively. The encapsulating material, due to its insulating nature and high optical transparency, surpasses that of ethylene–vinyl acetate (EVA), as demonstrated in this study. To assess the protective effect of the developed formulation, the study focused on applying the modified PLA resin onto isolated methylammonium lead iodide (MAPI) perovskite films on glass substrates. The samples were prepared as isolated MAPI absorbers to specifically assess the intrinsic contribution of the dual encapsulation configuration at its real position in a complete solar cell stack, demonstrating that even this unoptimized perovskite film exhibits remarkable stability and excellent structural and optical retention over two months under the protective scheme (86% of its initial structural stability, as quantified from integrated XRD peak intensities, and 68% of its initial optical absorbance, determined from the integrated UV–Vis spectra), whereas the uncoated films showed significant degradation. Although MAPI was selected as a model system due to its well-known environmental instability, the proposed encapsulation material and methodology are not limited to this architecture and can, in principle, be applied to various photovoltaic technologies. These findings demonstrate the strong potential of the polylactic-based resin as an effective environmental barrier for solar cells and provide a solid foundation for future full-device integration studies. Full article

The weak hydrogen bond with methylammonium iodide (MAI) dominates the formation of methylammonium lead iodide (MAPbI₃) during its nucleation and growth process. Herein, a weak hydrogen bond involving iodide is designed between the MAI and glycerol molecule in mixed solvents containing N, N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) to delay the growth of MAPbI₃ film. Incorporation of glycerol into the perovskite film indicates a larger grain size and suppressed nonradiative recombination of carriers in the film. Finally, the glycerol-doped perovskite solar cells (PSCs) achieve a champion power conversion efficiency (PCE) of up to 16.84%, with excellent stability to retain 92.05% of their initial PCE after 30 days of storage. The above results unveil a deep understanding of weak hydrogen bonds in high-performance perovskite photovoltaics. Full article

Lead halide perovskites, exemplified by methylammonium (MA) lead iodide (MAPbI₃), combine strong optical absorption, long carrier diffusion lengths, and defect-tolerant electronic structure with facile processing, making them attractive for photovoltaics and radiation detection. Yet, their behavior under electron irradiation remains insufficiently understood, limiting deployment in space and dosimetry contexts. Here, we employ Monte Carlo simulations (Geant4) to model electron interactions with MAPbI₃ across energies from 0.1 to 100 MeV and absorber thicknesses from 10 μm to 1 cm. We quantify deposited energy, event statistics, energy per interaction, non-ionizing energy loss, and dominant radiation effects. The results reveal strong thickness-dependent regimes: thin photovoltaic-type layers (~hundreds of nanometers) are largely transparent to MeV electrons, minimizing bulk damage but allowing localized ionization, exciton self-trapping, and photoexcitation-driven ion migration. Although localized excitations can temporarily improve carrier collection under short-term exposure, their cumulative effect drives ionic rearrangement and defect growth, ultimately reducing device stability. In contrast, thicker detector-type films (10–100 μm) sustain multiple scattering and ionization cascades, enhancing sensitivity but accelerating defect accumulation. At centimeter scales, energy deposition saturates, enabling bulk-like absorption for high-flux dosimetry. Overall, electron irradiation in MAPbI₃ is dominated by electronic excitation rather than ballistic displacements, underscoring the need to optimize thickness and composition to balance efficiency, sensitivity, and durability. Full article

Methylammonium lead iodide (MAPbI₃) perovskite has been widely studied for its optoelectronic properties, but its polycrystalline thin films inevitably contain grain boundaries and defects that degrade performance and stability. PbI₂ is often considered a destabilizing agent in perovskites, yet it has also been reported to act as a passivation agent, making its role a subject of debate. Here, we performed integrated optical, photoluminescence (PL), and ultra-low-frequency Raman mapping on a 100 μm² region of MAPbI₃ thin films to study the roles of PbI₂. The analyses resolved α-phase MAPbI₃-rich, PbI₂-rich, and mixed-phase domains, revealing heterogeneous PbI₂ distribution with PL quenching at defect sites. In addition, after light-induced degradation, PL changes were governed by both the local microstructure and PbI₂ distribution. Notably, PbI₂-rich regions retained PL, evidencing a protective passivation effect. These findings demonstrate that the beneficial role of PbI₂ is key to designing more stable perovskite devices. Full article

In this study, a UVC photodetector (PD) was fabricated by incorporating CsI into a conventional double-cation perovskite (FAMAPbI₃) to enhance its stability. The device utilized a methylammonium iodide post-treatment solution to fabricate CsFAMAPbI₃ perovskite thin films, which functioned as the primary light-absorbing layer in an NIP structure composed of n-type SnO₂ and p-type spiro-OMeTAD. Perovskite films were fabricated and analyzed as a function of the Cs concentration to optimize the Cs content. The results demonstrated that Cs doping improved the crystallinity and phase stability of the films, leading to their enhanced electron mobility and photodetection performance. The UVC PD with an optimum Cs concentration exhibited a responsivity of 58.2 mA/W and a detectivity of 3.52 × 10¹⁴ Jones, representing an approximately 7% improvement over conventional structures. Full article

Perovskite solar cells (PSCs) have already been reported as a promising alternative to traditional energy sources due to their excellent power conversion efficiency, affordability, and versatility, which is particularly relevant considering the growing worldwide demand for energy and increasing scarcity of natural resources. However, operational concerns under environmental stresses hinder its economic feasibility. Through the addition of cesium (Cs), this study investigates how to optimize perovskite solar cells (PSCs) based on methylammonium lead-iodide (MAPbI₃) by creating mixed-cation compositions of MA_1−xCs_xPbI₃ (x = 0, 0.25, 0.5, 0.75, 1) for devices A to E, respectively. The impact of cesium content on the following factors, such as open-circuit voltage (V_oc), short-circuit current density (J_sc), fill factor (FF), and power conversion efficiency (PCE), was investigated using simulation software, with ITO/TiO₂/MA_1−xCs_xPbI₃/Spiro-OMeTAD/Au as a device architecture. Due to diminished defect density, the device with x = 0.5 (MA_0.5Cs_0.5PbI₃) attains a maximum power conversion efficiency of 18.53%, with a V_oc of 0.9238 V, J_sc of 24.22 mA/cm², and a fill factor of 82.81%. The optimal doping density of TiO₂ is approximately 10²⁰ cm⁻³, while the optimal thicknesses of the electron transport layer (TiO₂, 10–30 nm), the hole-transport layer (Spiro-OMeTAD, about 10–20 nm), and the perovskite absorber (750 nm) were identified to maximize efficiency. The inclusion of a small amount of Cs may improve photovoltaic responses; however, at elevated concentrations (x > 0.5), power conversion efficiency (PCE) diminished due to the presence of trap states. The results show that mixed-cation perovskite solar cells can be a great commercially viable option because they strike a good balance between efficiency and performance. Full article

This study addresses the challenges of efficient, large-scale production of flexible transparent conducting electrodes (TCEs). We fabricate TCEs on polyethylene terephthalate (PET) substrates using a high-speed roll-to-roll (R2R) compatible method that combines gravure printing and photonic curing. The hybrid TCEs consist of Ag metal bus lines (Ag MBLs) coated with silver nanowires (AgNWs) and indium zinc oxide (IZO) layers. All materials are solutions deposited at speeds exceeding 10 m/min using gravure printing. We conduct a systematic study to optimize coating parameters and tune solvent composition to achieve a uniform AgNW network. The entire stack undergoes photonic curing, a low-energy annealing method that can be completed at high speeds and will not damage the plastic substrates. The resulting hybrid TCEs exhibit a transmittance of 92% averaged from 400 nm to 1100 nm and a sheet resistance of 11 Ω/sq. Mechanical durability is tested by bending the hybrid TCEs to a strain of 1% for 2000 cycles. The results show a minimal increase (<5%) in resistance. The high-throughput potential is established by showing that each hybrid TCE fabrication step can be completed at 30 m/min. We further fabricate methylammonium lead iodide solar cells to demonstrate the practical use of these TCEs, achieving an average power conversion efficiency (PCE) of 13%. The high-performance hybrid TCEs produced using R2R-compatible processes show potential as a viable choice for replacing vacuum-deposited indium tin oxide films on PET. Full article

We herein report the enhanced electrical properties of self-powered perovskite-based photodetectors with high sensitivity and responsivity by applying the surface passivation strategy using C₆₀ (fullerene) as a surface passivating agent. The perovskite (CH₃NH₃PbI₃) thin film passivated with fullerene achieves a highly uniform and compact surface, showing reduced leakage current and higher photon-to-current conversion capability. As a result, the improved film quality of the perovskite layer allows excellent photon-detecting properties, including high values of external quantum efficiency (>95%), responsivity (>5 A W⁻¹), and specific detectivity (>10¹³ Jones) at zero bias voltage, which surpasses those of the pristine perovskite-based device. Furthermore, the passivated device showed fast rise (0.18 μs) and decay times (17 μs), demonstrating high performance and ultrafast light-detecting capability of the self-powered perovskite-based photodetectors. 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

Hybrid organohalide perovskites have received considerable attention due to their exceptional photovoltaic (PV) conversion efficiencies in optoelectronic devices. In this study, we report the development of a highly sensitive, self-powered perovskite-based photovoltaic photodiode (PVPD) fabricated by incorporating a poly(amic acid)-polyimide (PAA-PI) copolymer as an interfacial layer between a methylammonium lead iodide (CH₃NH₃PbI₃, MAPbI₃) perovskite light-absorbing layer and a poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT: PSS) hole injection layer. The PAA-PI interfacial layer effectively suppresses carrier recombination at the interfaces, resulting in a high power conversion efficiency (PCE) of 11.8% compared to 10.4% in reference devices without an interfacial layer. Moreover, applying the PAA-PI interfacial layer to the MAPbI₃ PVPD significantly improves the photodiode performance, increasing the specific detectivity by 49 times to 7.82 × 10¹⁰ Jones compared to the corresponding results of reference devices without an interfacial layer. The PAA-PI-passivated MAPbI₃ PVPD also exhibits a wide linear dynamic range of ~103 dB and fast response times, with rise and decay times of 61 and 18 µs, respectively. The improved dynamic response of the PAA-PI-passivated MAPbI₃ PVPD enables effective weak-light detection, highlighting the potential of advanced interfacial engineering with PAA-PI interfacial layers in the development of high-performance, self-powered perovskite photovoltaic photodetectors for a wide range of optoelectronic applications. Full article

Building-integrated photovoltaic (BIPV) glazing systems with intelligent window technologies enhance building energy efficiency by generating electricity and managing daylighting. This study explores advanced BIPV glazing, focusing on building-integrated concentrating photovoltaic (BICPV) systems. BICPV integrates concentrating optics, such as holographic films, luminescent solar concentrators (LSC), Fresnel lenses, and compound parabolic concentrators (CPCs), with photovoltaic cells. Notable results include achieving 17.9% electrical efficiency using cylindrical holographic optical elements and crystalline silicon cells at a 3.5× concentration ratio. Dielectric CPCs showed 97.7% angular acceptance efficiency in simulations and 94.4% experimentally, increasing short-circuit current and maximum power by 87.0% and 96.6%, respectively, across 0° to 85° incidence angles. Thermochromic hydrogels and thermotropic smart glazing systems demonstrated significant HVAC energy savings. Large-area 1 m² PNIPAm-based thermotropic window outperformed conventional double glazing in Singapore. The thermotropic parallel slat transparent insulation material (TT PS-TIM) improved energy efficiency by up to 21.5% compared to double glazing in climates like London and Rome. Emerging dynamic glazing technologies combine BIPV with smart functions, balancing transparency and efficiency. Photothermally controlled methylammonium lead iodide PV windows achieved 68% visible light transmission, 11.3% power conversion efficiency, and quick switching in under 3 min. Polymer-dispersed liquid crystal smart windows provided 41–68% visible transmission with self-powered operation. Full article

The recombination of charges and thermal excitation of carriers at the interface between methylammonium lead iodide perovskite (PVK) and the carbon electrode are crucial factors that affect the optoelectronic performance of carbon-based hole transport layer (HTL)-free perovskite photodetectors. In this work, a method was employed to introduce SnS quantum dots (QDs) on the back surface of perovskite, which passivated the defect states on the back surface of perovskite and addressed the energy-level mismatch issue between perovskite and carbon electrode. Performance testing of the QDs and the photodetector revealed that SnS QDs possess energy-level structures that are well matched with perovskite and have high absorption coefficients. The incorporation of these QDs into the interface layer effectively suppresses the dark current of the photodetector and greatly enhances the utilization of incident light. The experimental results demonstrate that the introduction of SnS QDs reduces the dark current by an order of magnitude compared to the pristine device at 0 V bias and increases the responsivity by 10%. The optimized photodetector exhibits a wide spectral response range (350 nm to 750 nm), high responsivity (0.32 A/W at 500 nm), and high specific detectivity (>1 × 10¹² Jones). Full article