Search Results (191)

In high energy density physics, the demand for precise detection of nanosecond-level fast physical processes is high. Ga:ZnO (GZO), GaN, and other fast scintillators are widely used in pulsed signal detection. However, many of them, especially wide-bandgap materials, still face issues of low luminous intensity and significant self-absorption. Therefore, an enhanced method was proposed to tune the wavelength of materials via coating perovskite quantum dot (QD) films. Three-layer samples based on GZO were primarily investigated and characterized. Radioluminescence (RL) spectra from each face of the samples, as well as their decay times, were obtained. Lower temperatures further enhanced the luminous intensity of the samples. Its overall luminous intensity increased by 2.7 times at 60 K compared to room temperature. The changes in the RL processes caused by perovskite QD and low temperatures were discussed using the light tuning and transporting model. In addition, an experiment under a pico-second electron beam was conducted to verify their pulse response and decay time. Accordingly, the samples were successfully applied in beam state monitoring of nanosecond pulsed proton beams, which indicates that GZO wafer coating with perovskite QD films has broad application prospects in pulsed radiation detection. Full article

Lead halide perovskite quantum dots, also known as perovskite nanocrystals, are considered one of the most promising photovoltaic materials for solar cells due to their outstanding optoelectronic properties and simple preparation techniques. The key factors restricting the photoelectric conversion efficiency of solar cell systems are the separation and transmission performances of charge carriers. Here, femtosecond time-resolved ultrafast spectroscopy was used to measure the interfacial charge transfer dynamics of different sizes of CsPbBr₃ assembled with TiO₂. The effect of perovskite size on the charge transfer is discussed. According to our experimental data analysis, the time constants of the interfacial electron transfer and charge recombination of the assembled systems of CsPbBr₃ and titanium dioxide become larger when the size of the CsPbBr₃ nanocrystals increases. We discuss the physical mechanism by which the size of perovskites affects the rate of charge transfer in detail. We expect that our experimental results provide experimental support for the application of novel quantum dots for solar cell materials. Full article

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

Perovskite quantum dots (PVK QDs) are gaining significant attention as potential materials for next-generation memory devices leveraged by their ion dynamics, quantum confinement, optoelectronic synergy, bandgap tunability, and solution-processable fabrication. In this review paper, we explore the fundamental characteristics of organic/inorganic halide PVK QDs and their role in resistive switching memory architectures. We provide an overview of halide PVK QDs synthesis techniques, switching mechanisms, and recent advancements in memristive applications. Special emphasis is placed on the ionic migration and charge trapping phenomena governing resistive switching, along with the prospects of photonic memory devices that leverage the intrinsic photosensitivity of PVK QDs. Despite their advantages, challenges such as stability, scalability, and environmental concerns remain critical hurdles. We conclude this review with insights into potential strategies for enhancing the reliability and commercial viability of PVK QD-based memory technologies. 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

Intense circularly polarized luminescence is crucial for high-performance electroluminescent, optoelectronic, and photonic devices. This study investigates the magneto-chiral characteristics of two achiral soluble diamagnetic perovskite-type PbQDs. Magnetic fields of 158 and 198 mT are applied using an electromagnet in a toluene solution at 25 °C. Both PbQDs show a magnetic circularly polarized luminescence magnitude of approximately 10⁻³ within the (480 to 580) nm wavelength range. The strength of the magnetic circularly polarized luminescence increases with the intensity of the applied magnetic field. Furthermore, the study demonstrates rapid and reversible switching of the rotation direction of the magnetic circularly polarized luminescence when the magnetic poles are rapidly changed. These results suggest that the direction (right- and left-rotating light) and circular polarization of circularly polarized luminescence (CPL) from circularly polarized perovskites can be alternately and freely controlled by applying an external magnetic field with an appropriate direction and strength. Full article

Coupling organic light-harvesting materials with lead halide perovskite quantum dots (LHP QDs) is an attractive approach that could provide great potential in optoelectronic applications owing to the diversity of organic materials available and the intriguing optical and electronic properties of LHP QDs. Here, we demonstrate energy collection by CsPbI₃ QDs from a near-infrared (NIR) light-harvesting upconversion system. The upconversion system consists of Pd-tetrakis-5,10,15,20-(p-methoxycarbonylphenyl)-tetraanthraporphyrin (PdTAP) as the sensitizer to harvest NIR photons and rubrene as the annihilator to generate upconverted photons via triplet fusion. Steady-state and time-resolved photoluminescence spectra reveal that CsPbI₃ QDs are energized via radiative energy transfer from the singlet excited rubrene with photophysics fidelity of respective components. In addition, a volumetric display demo incorporating CsPbI₃ QDs as light emitters employing triplet fusion upconversion was developed, showing bright luminescent images from CsPbI₃ QDs. These results present the feasibility of integrating organic light-harvesting systems and perovskite QDs, enabling diverse light harvesting and activation of perovskite materials for optoelectronic applications. Full article

The traditional von Neumann architecture encounters significant limitations in computational efficiency and energy consumption, driving the development of neuromorphic devices. The optoelectronic synaptic device serves as a fundamental hardware foundation for the realization of neuromorphic computing and plays a pivotal role in the development of neuromorphic chips. This study develops a ternary heterojunction synaptic transistor based on perovskite quantum dots to tackle the critical challenge of synaptic weight modulation in organic synaptic devices. Compared to binary heterojunction synaptic transistor, the ternary heterojunction synaptic transistor achieves an enhanced hysteresis window due to the synergistic charge-trapping effects of acceptor material and perovskite quantum dots. The memory window decreases with increasing source-drain voltage (V_DS) but expands with prolonged program/erase time, demonstrating effective carrier trapping modulation. Furthermore, the device successfully emulates typical photonic synaptic behaviors, including excitatory postsynaptic currents (EPSCs), paired-pulse facilitation (PPF), and the transition from short-term plasticity (STP) to long-term plasticity (LTP). This work provides a simplified strategy for high-performance optoelectronic synaptic transistors, showcasing significant potential for neuromorphic computing and adaptive intelligent systems. Full article

Perovskite quantum dots (PQDs), with their excellent optical properties, have become a leading semiconductor material in the field of optoelectronics. However, to date, it has been a challenge to achieve the three-dimensional high-resolution patterning of perovskite quantum dots. In this paper, an in situ femtosecond laser-direct-writing technology was demonstrated for three-dimensional high-resolution patterned CsPbBr₃ PQDs using a two-photon photoresist nanocomposite doped with the CsPbBr₃ perovskite precursor. By adjusting the laser processing parameters, the minimum line width of the PQDs material was confirmed to be 98.6 nm, achieving a sub-100 nm PQDs nanowire for the first time. In addition, the fluorescence intensity of the laser-processed PQDs can be regulated by the laser power. Our findings provide a new technology for fabricating high-resolution display devices based on laser-direct-writing CsPbBr₃ PQDs materials. Full article

The variable bandgap and high absorption coefficient of all-inorganic halide perovskite quantum dots (QDs), particularly CsPbBr₂I make them highly promising for photodetector applications. However, their high defect density and poor stability limit their performance. To overcome these problems, Mn²⁺-doped CsPbBr₂I QDs with varying concentrations were synthesized via the one-pot method in this work. By replacing Pb²⁺ ions, moderate Mn²⁺ doping caused lattice contraction and improved crystallinity. At the same time, Mn²⁺-doping effectively passivated surface defects, reducing the defect density by 33%, and suppressed non-radiative recombination, thereby improving photoluminescence (PL) intensity and carrier mobility. The optimized Mn:CsPbBr₂I QDs-based photodetector exhibited superior performance, with a dark current of 1.19 × 10⁻¹⁰ A, a photocurrent of 1.29 × 10⁻⁵ A, a responsivity (R) of 0.83 A/W, a specific detectivity (D*) of 3.91 × 10¹² Jones, an on/off ratio up to 10⁵, and the response time reduced to less than 10 ms, all outperforming undoped CsPbBr₂I QDs devices. Stability tests demonstrated enhanced durability, retaining 80% of the initial photocurrent after 200 s of cycling (compared to 50% for undoped devices) and stable operation over 20 days. This work offers a workable strategy for rational doping and structural optimization in the construction of high-performance perovskite optoelectronic devices. Full article

Recently, the numerical simulation of solar cells has attracted tantamount scientific attention in the photovoltaic community because it saves on research time and resources before the actual fabrication of the devices in the laboratories. Despite significant advancements in the fabrication of quantum dot-sensitized solar cells (QDSSCs), the power conversion efficiency (PCE) is still low when compared to other solar cells such as perovskite. This efficiency gap poses a substantial challenge in harnessing the full potential of QDSSCs for widespread adoption in renewable energy applications. Enhancing the efficiency of QDSSCs is imperative for their commercial viability and widespread deployment. In this work, SCAPS-1D was used in the simulation of QDSSCs. The solar cell with a general configuration of FTO/TiO₂/PbS/HTL/Au was investigated. In the device, PbS quantum dots were inserted as the absorber layer, TiO₂ as the electron transport layer (ETL), gold as the back contact, and the following inorganic materials, i.e., copper (I) iodide (CuI), copper (I) oxide (Cu₂O), cadmium zinc telluride selenide (CZTSe), copper iron tin sulfide (CFTS), and copper zinc tin sulfide selenide (CZTSSe) were tested as HTL materials, and FTO acted as the conductive substrate. The best HTL material (CZTSSe) exhibited a PCE of 22.61%, with a fill factor (FF) of 84.67%, an open circuit voltage (V_oc) of 0.753 V, and a current density (J_sc) of 35.48 mA cm⁻². This study contributes to the field by employing SCAPS-1D simulations to optimize QDSSCs, exploring novel inorganic HTL materials for these solar cells and identifying CZTSSe as a promising low-cost HTL that significantly enhances both the performance and commercial viability of QDSSCs. Full article

Monolayer MoS₂ has been widely researched in high performance phototransistors for its high carrier mobility and strong photoelectric conversion ability. However, some defects in MoS₂, such as vacancies or impurities, provide more possibilities for carrier recombination; thus, restricting the formation of photocurrents and resulting in decreased responsiveness. Herein, all-inorganic CsPbBr₃ perovskite quantum dots (QDs) with high photoelectric conversion efficiency and light absorption coefficients are introduced to enhance the responsivity of a 2D MoS₂ phototransistor. The CsPbBr₃/MoS₂ heterostructure has a type II energy band, and it has a high responsivity of ~1790 A/W and enhanced detectivity of ~2.4 × 10¹¹ Jones. Additionally, the heterostructure CsPbBr₃/MoS₂ enables the synergistic effect mechanism of photoconduction and photogating effects with the gate tunable photo-response, which could also contribute to an improved performance of the MoS₂ phototransistor. This work provides new strategies for performance phototransistors and is expected to play an important role in many fields, such as optical communication, environmental monitoring and biomedical imaging, and promote the development and application of related technologies. Full article

Metal halide perovskite quantum dots (MHP QDs), as a kind of fluorescent material, have attracted much attention due to their excellent photoluminescence (PL) quantum yield (QY), narrow full width at half maximum (FWHM), broad absorption, and tunable emission wavelength. However, the instability and biological incompatibility of MHP QDs greatly hinder their application in the field of biomedicine. Hydrogels are three-dimensional polymer networks that are widely used in biomedicine because of their high transparency and excellent biocompatibility. This review not only introduces the latest research progress in improving the mechanical and optical properties of hydrogels/MHP QDs but also combines it with the existing methods for enhancing the stability of MHP QDs in hydrogels, aiming to provide new ideas for researchers in material selection and methods for constructing MHP QD-embedded hydrogels. Finally, their application prospects and future challenges are introduced. Full article

We have estimated the intrinsic complex refractive index spectrum of a CsPbBr₃ nanocrystal. With various dilute solutions of CsPbBr₃ nanocrystals dissolved in toluene, effective refractive indices were measured at two different wavelengths using Michelson interferometry. Given the effective absorption spectrum of the solution, a full spectrum of the effective refractive index was also obtained through the Kramers–Krönig relations. Based on the Maxwell–Garnett model in the effective medium approximation, the real and imaginary spectrum of the complex refractive index was estimated for the CsPbBr₃ nanocrystal, and the dominant inaccuracy was attributed to the size inhomogeneity. Full article

Abstract: Quantum dot–polymer composites have the advantages of high luminescent quantum yield (PLQY), narrow emission half-peak full width (FWHM), and tunable emission spectra, and have broad application prospects in display and lighting fields. Research on quantum dots embedded in polymer films and plates has made great progress in both synthesis technology and optical properties. However, due to the shortcomings of quantum dots, such as cadmium selenide (CdSe), indium phosphide (InP), lead halide perovskite (LHP), poor water, oxygen, and light stability, and incapacity for large-scale synthesis, their practical application is still restricted. Various polymers, such as methyl methacrylate (PMMA), polyethylene terephthalate (PET), polystyrene (PS), polyvinylidene fluoride (PVDF), polypropylene (PP), etc., are widely used in packaging quantum dot materials because of their high plasticity, simple curing, high chemical stability, and good compatibility with quantum dot materials. This paper focuses on the application and development of quantum dot–polymer materials in the field of backlight displays, summarizes and expounds the synthesis strategies, advantages, and disadvantages of different quantum dot–polymer materials, provides inspiration for the optimization of quantum dot–polymer materials, and promotes their application in the field of wide-color-gamut backlight display. Full article