Search Results (110)

Artificial photoelectric synapses exhibit great potential for overcoming the Von Neumann bottleneck in computational systems. All-inorganic halide perovskites hold considerable promise in photoelectric synapses due to their superior photon-harvesting efficiency. In this study, a novel wavy-structured CsPbBr₃/ZnO hybrid film was realized by depositing zinc oxide (ZnO) onto island-like CsPbBr₃ film via atomic layer deposition (ALD) at 70 °C. Due to the capability of ALD to grow high-quality films over small surface areas, dense and thin ZnO film filled the gaps between the island-shaped CsPbBr₃ grains, thereby enabling reduced light-absorption losses and efficient charge transport between the CsPbBr₃ light absorber and the ZnO electron-transport layer. This ZnO/island-like CsPbBr₃ hybrid synaptic transistor could operate at a drain-source voltage of 1.0 V and a gate-source voltage of 0 V triggered by green light (500 nm) pulses with low light intensities of 0.035 mW/cm². The device exhibited a quiescent current of ~0.5 nA. Notably, after patterning, it achieved a significantly reduced off-state current of 10⁻¹¹ A and decreased the quiescent current to 0.02 nA. In addition, this transistor was able to mimic fundamental synaptic behaviors, including excitatory postsynaptic currents (EPSCs), paired-pulse facilitation (PPF), short-term to long-term plasticity (STP to LTP) transitions, and learning-experience behaviors. This straightforward strategy demonstrates the possibility of utilizing neuromorphic synaptic device applications under low voltage and weak light conditions. Full article

This study aims to enhance optoelectronic properties of all-inorganic perovskite photodetectors (PDs) by incorporating a bilayer electron transport layer (ETL). The bilayer ETL composed of SnO₂ and ZnO effectively optimizes energy level alignment at the interface, facilitating efficient electron extraction from the CsPbI₂Br perovskite layer while suppressing shunt pathways. Additionally, it enhances interfacial properties by mitigating defects and minimizing dark current leakage, thereby improving overall device performance. As a result, the bilayer ETL-based PDs exhibit broadband photoresponsivity in 300 to 700 nm with a responsivity of 0.45 A W⁻¹ and a specific detectivity of 9 × 10¹³ Jones, outperforming the single-ETL devices. Additionally, they demonstrate stable cyclic photoresponsivity with fast response times (14 μs for turn-on and 32 μs for turn-off). The bilayer ETL also improves long-term reliability and thermal stability, highlighting its potential for high performance, reliability, and practical applications of all-inorganic perovskite PDs. Full article

The increasing spread of infectious diseases caused by pathogenic microorganisms underscores the urgent need for highly sensitive, portable, and rapid nucleic acid detection technologies to facilitate early diagnosis and effective prevention. In this study, we developed a fluorescence-based nucleic acid detection platform that integrates a microfluidic chip with an all-inorganic perovskite photodetector. The system enables integrated operation of nucleic acid extraction, purification, and amplification on a microfluidic chip, combined with real-time electrical signal readout via a CsPbBr₃ perovskite photodetector. Experimental results indicate that the photodetector exhibits high responsivity at 530 nm, aligning well with the primary emission peak of FAM. The system demonstrates a strong linear correlation between photocurrent and FAM concentration over the range of 0.01–0.4 μM (R² = 0.928), with a low detection limit of 0.01 μM and excellent reproducibility across multiple measurements. Validation using FAM standard solutions and Escherichia coli samples confirmed the system’s reliable linearity and signal stability. This platform demonstrates strong potential for rapid pathogen screening and point-of-care diagnostic applications. Full article

The persistent operational instability of all-inorganic cesium lead halide (CsPbX₃) perovskite nanocrystals (NCs) has hindered their integration into white-light-emitting diodes (WLEDs). This study introduces a transformative approach by engineering a phase transition from CsPbBr₃ NCs to zirconium bromide (ZrBr₄)-stabilized hexagonal nanocomposites (HNs) through a modified hot-injection synthesis. Structural analyses revealed that the ZrBr₄-mediated phase transformation induced a structurally ordered lattice with minimized defects, significantly enhancing charge carrier confinement and radiative recombination efficiency. The resulting HNs achieved an exceptional photoluminescence quantum yield (PLQY) of 92%, prolonged emission lifetimes, and suppressed nonradiative decay, attributed to effective surface passivation. The WLEDs with HNs enabled a breakthrough luminous efficiency of 158 lm/W and a record color rendering index (CRI) of 98, outperforming conventional CsPbX₃-based devices. The WLEDs exhibited robust thermal stability, retaining over 80% of initial emission intensity at 100 °C, and demonstrated exceptional operational stability with negligible PL degradation during 50 h of continuous operation at 100 mA. Commission Internationale de l’Éclairage (CIE) coordinates of (0.35, 0.32) validated pure white-light emission with high chromatic fidelity. This work establishes ZrBr₄-mediated HNs as a paradigm-shifting material platform, addressing critical stability and efficiency challenges in perovskite optoelectronics and paving the way for next-generation, high-performance lighting solutions. Full article

All-inorganic CsPbX₃ perovskites have significant potential for applications in the photovoltaic field. However, during their preparation, the slow evaporation rate of the precursor solution limits the extent of solution supersaturation, leading to porous perovskite films that substantially impair device performance. Anti-solvent engineering, which introduces a secondary solvent to modulate the crystallization process, is a well established technique in perovskite photovoltaic research. This study systematically examines the effects of four different anti-solvents on perovskite films and corresponding devices. It also investigates the optimal dipping-time of (trifluoromethyl)benzene as an anti-solvent, as well as the impact of varying amounts of anti-solvent additive perfluorinated acid. The optimized devices achieved a maximum power conversion efficiency of 12.68%. Full article

Layered perovskites have been actively studied due to their outstanding electronic and optical properties as well as kinetic stability. Layered perovskites with hexagonal symmetry have special electronic properties, such as the Dirac cone in the band structure, similar to graphene. In the presented study, the heterostructure of single-layer all-inorganic lead-free hexagonal perovskite of the A₃B₂X₉ type (A = Cs, Rb, K; B = In, Sb; X = Cl, Br) and graphene (Gr) was studied. The structural and electronic characteristics of A₃B₂X₉ and the A₃B₂X₉/Gr composite were calculated using density functional theory. It was found that graphene is not deformed, while the main deformation is observed only in perovskite. B-X bonds have different sensitivities to stretching or compression. The Fermi level of the A₃In₂X₉/Gr composite can be shifted down from the Dirac point, which can be used to create optoelectronic devices or as spacer layers for graphene-based resonant tunneling nanostructures. 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

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

The CsPbBr₃ perovskite exhibits strong environmental stability under light, humidity, temperature, and oxygen conditions. However, in all-inorganic perovskite solar cells (PSCs), interface defects between the carbon electrode and CsPbBr₃ limit the carrier separation and transfer rates. We used black phosphorus (BP) nanosheets as the hole transport layer (HTL) to construct an all-inorganic carbon-based CsPbBr₃ perovskite (FTO/c-TiO₂/m-TiO₂/CsPbBr₃/BP/C) solar cell. BP can enhance hole extraction capabilities and reduce carrier recombination by adjusting the interface contact between the perovskite and the carbon layer. Due to the coordination of the energy structure related to interface charge extraction and transfer, BP, as a new type of hole transport layer for all-inorganic CsPbBr₃ solar cells, achieves a power conversion efficiency (PCE) that is 1.43% higher than that of all-inorganic carbon-based CsPbBr₃ perovskite solar cells without a hole transport layer, reaching 2.7% (Voc = 1.29 V, Jsc = 4.60 mA/cm², FF = 48.58%). In contrast, the PCE of the all-inorganic carbon-based CsPbBr₃ perovskite solar cells without a hole transport layer was only 1.27% (Voc = 1.22 V, Jsc = 2.65 mA/cm², FF = 39.51%). The unencapsulated BP-based PSCs device maintained 69% of its initial efficiency after being placed in the air for 500 h. In contrast, the efficiency of the PSC without HTL significantly decreased to only 52% of its initial efficiency. This indicates that BP can effectively enhance the PCE and stability of PSCs, demonstrating its great potential as a hole transport material in all-inorganic perovskite solar cells. BP as the HTL for CsPbBr₃ PSCs can passivate the perovskite interface, enhance the hole extraction capability, and improve the optoelectronic performance of the device. The subsequent doping and compounding of the BP hole transport layer can further enhance its photovoltaic conversion efficiency in PSCs. Full article

This study reviews the advanced anti-counterfeiting applications of CsCdCl₃, a lead-free all-inorganic perovskite crystal exhibiting dynamic luminescent properties responsive to temperature and UV light. Using synthesis methods such as Bridgman and hydrothermal techniques and incorporating dopants like bromine and tellurium, this research achieves improved luminescent stability, spectral diversity, and afterglow characteristics in CsCdCl₃. The crystal demonstrates extended afterglow, photochromic shifts, and temperature-sensitive luminescence, enabling applications in 4D encoding for secure data encryption and in cold-chain temperature monitoring for pharmaceuticals. Despite these promising attributes, the challenges related to photostability, batch consistency, and environmental resilience persist, necessitating further exploration into the optimized synthesis and doping strategies to enhance material stability. These findings underscore the potential of CsCdCl₃ for high-security information storage, pharmaceutical anti-counterfeiting, and real-time environmental sensing, positioning it as a valuable material for the next generation of secure, intelligent packaging solutions. Full article

Perovskite materials, as emerging semiconductors, have attracted significant attention for their exceptional optoelectronic properties, tunable bandgaps, ease of fabrication, and cost-effectiveness, making them promising candidates for next-generation optoelectronic devices. The all-inorganic perovskite Cs₂AgBiBr₆ distinguishes itself from other perovskite materials due to its remarkable optical absorption and emission properties, excellent stability, prolonged carrier recombination lifetime, and nontoxic characteristics. However, a deeper understanding of its unique luminescent properties and a further optimization of its structure and performance are still necessary. This study systematically investigates the optimization of Cs₂AgBiBr₆ double perovskite films through A-site Na⁺ doping. At an optimal Na⁺ doping concentration of 3.5% (Na_0.07Cs_1.93AgBiBr₆), the film shows 1.4 times and 2.7 times enhancement in light absorption and photoluminescence intensity, compared to the undoped film. Low-temperature spectroscopy measurements indicate that Na_0.07Cs_1.93AgBiBr₆ exhibits higher exciton binding energy and phonon energy. Based on Na_0.07Cs_1.93AgBiBr₆, the photodetectors demonstrate significant performance improvements, with a high photocurrent response of 10⁻² A, a photo-to-dark current ratio (PDCR) of 7.57 × 10⁴, a responsivity (R) of 16.23 A/W, a detectivity (D*) of 2.92 × 10¹² Jones, a linear dynamic range (LDR) of 98.75 dB, and a fast response time of 943 ms. This work provides a promising strategy for optimizing all-inorganic perovskite materials through doping and offers guidance for enhancing high-performance photodetectors. Full article

All-inorganic perovskite materials are promising in optoelectronics, but their morphology is a key parameter for achieving high device efficiency. We prepared CsPbBr₃ perovskite microcrystals with different shapes grown directly on planar substrate by conventional drop casting. We observed the formation of CsPbBr₃ microcubes on bare indium tin oxide (ITO)-coated glass. Interestingly, with the same technique, CsPbBr₃ microrods were obtained on (3-Aminopropyl) triethoxysilane (APTES)-modified ITO-glass, which we ascribe to the modification of formation kinetics. The obtained microcrystals exhibit an orthorhombic structure. A green photoluminescence (PL) emission is revealed from the CsPbBr₃ microrods. Contact angle measurements, Fourier-transform infrared and PL spectroscopies confirmed that APTES linked successfully to the ITO-glass substrate. We propose a qualitative mechanism to explain the anisotropic growth. The microrods exhibited improved PL and a slower PL lifetime compared to the microcubes, likely due to the diminished occurrence of defects. This work demonstrates the importance of the substrate surface to control the growth of perovskite single crystals and to boost the radiative recombination in view of high-performance optoelectronic devices. Full article

All-inorganic CsPbBr₃ perovskite solar cells have garnered extensive attention in the photovoltaic domain due to their remarkable environmental stability. Nevertheless, CsPbBr₃ prepared using the conventional sequential deposition method suffers from issues such as inferior crystallinity, low phase purity, and poor film morphology. Herein, we propose a pre-crystallization methodology by introducing a minute quantity of CsBr into the PbBr₂ precursor solution to generate a small amount of CsPb₂Br₅ crystals within the PbBr₂ film, leading to a porous PbBr₂ film with enhanced crystallinity. Under the influence of more pores and CsPb₂Br₅ crystals as nucleation sites for inducing growth, a CsPbBr₃ film with a larger crystal size, lower grain boundary density, stronger crystallinity, and higher phase purity is formed. Compared with untreated devices, photovoltaic devices prepared using the pre-crystallization method achieved a champion photovoltaic conversion efficiency (PCE) of 8.62%. Furthermore, pre-crystallized devices demonstrate higher stability than untreated ones and can still retain 94% of the original PCE after being exposed to air for 1000 h without encapsulating. Full article

Inorganic CsPbX₃ (X = Cl, Br, I) perovskite quantum dots (PQDs) have attracted widespread attention due to their excellent optical properties and extensive application prospects. However, their inherent structural instability significantly hinders their practical application despite their outstanding optical performance. To enhance stability, an in situ electrospinning strategy was used to synthesize CsPbX₃/polyacrylonitrile composite nanofibers. By optimizing process parameters (e.g., halide ratio, electrospinning voltage, and heat treatment temperature), all-inorganic CsPbX₃ PQDs have been successfully grown in a polyacrylonitrile (PAN) matrix. During the electrospinning process, the rapid solidification of electrospun fibers not only effectively constrained the formation of large-sized PQDs but also provided effective physical protection for PQDs, resulting in the improvement in the water stability of PQDs by minimizing external environmental interference. Even after storage in water for over 100 days, the PQDs maintained approximately 93.5% of their photoluminescence intensity. Through the adjustment of halogen elements, the as-obtained composite nanofibers exhibited color-tunable luminescence in the visible light region, and based on this, a series of multicolor anti-counterfeiting patterns were fabricated. Additionally, benefiting from the excellent water stability and optical performance, the CsPbBr₃/PAN composite film was combined with red-emitting K₂SiF₆:Mn⁴⁺ (KSF) on a blue LED (460 nm), producing a stable and efficient WLED device with a color temperature of around 6000 K and CIE coordinates of (0.318, 0.322). These results provide a general approach to synthesizing PQDs/polymer nanocomposites with excellent water stability and multicolor emission, thereby promoting their practical applications in multifunctional optoelectronic devices and advanced anti-counterfeiting. Full article

In this research, SCAPS-1D simulation software (Version: 3.3.10) was employed to enhance the efficiency of CsSnX₃ (X = Cl, Br, I) all-inorganic perovskite solar cells. By fine-tuning essential parameters like the work function of the conductive glass, the back contact point, defect density, and the thickness of the light absorption layer, we effectively simulated the optimal performance of CsSnX₃ (X = Cl, Br, I) all-inorganic perovskite solar cells under identical conditions. The effects of different X-site elements on the overall performance of the device were also explored. The theoretical photoelectric conversion efficiency of the device gradually increases with the successive substitution of halogen elements (Cl, Br, I), reaching 6.09%, 17.02%, and 26.74%, respectively. This trend is primarily attributed to the increasing size of the halogen atoms, which leads to better light absorption and charge transport properties, with iodine (I) yielding the highest theoretical conversion efficiency. These findings suggest that optimizing the halogen element in CsSnX₃ can significantly enhance device performance, providing valuable theoretical guidance for the development of high-efficiency all-inorganic perovskite solar cells. Full article