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Charge extraction via graded doping of hole transport layers gives highly luminescent and stable metal halide perovskite devices
摘要： One source of instability in perovskite solar cells (PSCs) is interfacial defects, particularly those that exist between the perovskite and the hole transport layer (HTL). We demonstrate that thermally evaporated dopant-free tetracene (120 nm) on top of the perovskite layer, capped with a lithium-doped Spiro-OMeTAD layer (200 nm) and top gold electrode, offers an excellent hole-extracting stack with minimal interfacial defect levels. For a perovskite layer interfaced between these graded HTLs and a mesoporous TiO2 electron-extracting layer, its photoluminescence yield reaches 15% compared to 5% for the perovskite layer interfaced between TiO2 and Spiro-OMeTAD alone. For PSCs with graded HTL structure, we demonstrate efficiency of up to 21.6% and an extended power output of over 550 hours of continuous illumination at AM1.5G, retaining more than 90% of the initial performance and thus validating our approach. Our findings represent a breakthrough in the construction of stable PSCs with minimized nonradiative losses.
关键词： perovskite solar cells,stability,charge extraction,photoluminescence,hole transport layers,graded doping
更新于2025-11-14 15:25:21
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Addressing the Reliability and Electron Transport Kinetics in Halide Perovskite Film via Pulsed Laser Engineering
摘要： The long-term performance and stability of perovskites are adversely affected by their porous microstructure, tensile residual stress, and electron transport kinetics. Here, a high-speed pulsed laser processing technique is implemented to produce beneficial structural changes in organic–inorganic halide perovskites, including pore-free, crystalline structure, reduced defects, and tensile residual stress. Moreover, halide perovskite films can be converted from p-type to n-type semiconductor, which originates from crystal structure changes, giving rise to carrier dynamic changes. Comparing with traditional thermal annealing, residual tensile stress of perovskite thin film decreases by 40% after pulse laser processing, which significantly increases its stability. Pulse-laser-induced thermomechanical shock momentum can create pore-free perovskite thin films, contributing to much better reliability. Under humidity of 80% at room temperature for 500 h, the decomposition rate is reduced by more than two times, comparing thin films after pulsed laser processing with conventional thermal annealing. The thermal decomposition temperature of pulse-laser-processed perovskite thin film raises by 20 to about 220 °C. Pulse laser processing technique provides a scalable technique to tailor the structures in perovskite films with both temperature and loading control, further facilitates the design of perovskite-based devices for service under harsh conditions, and also contributes to high-performance optoelectronic applications.
关键词： semiconductors,perovskites,stability,microstructures,residual stress
更新于2025-11-14 15:24:45
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MAPbI3/agarose photoactive composite for highly stable unencapsulated perovskite solar cells in humid environment
摘要： Perovskite solar cells, bearing the merits of facile preparaion and remarkable efficiency, has great potential for bringing the photovoltaic industry to a new generation. The photovoltaic market demands high-efficiency, high stability and low-cost fabrication of perovksite solar cells, especially stability to the humid environment for operation. Here, MAPbI3/agarose photoactive material for humid stable unencapsulated devices has been proposed. These solar cells have been operated in ambient humid environment without glove box, exhibiting efficiency up to 14.66% and retain 90% of its PCE after 1392 h and 60% of initial PCE after 1972 h in ambient humid environment (RH>70%) without encapsulation. FTIR and XPS measurements reveal two critical factors for the improved stability. The molecular level interactions between agarose and MAPbI3 passivates the grain boundaries of perovskite thus preventing its degradation. Moreover, the formation of Li+-agarose complex at the interface between perovskite layer and hole conductive layer, effectively prevents the water uptake of MAPbI3 layer. Both effects of passivation and minimization of hygroscopicity of LiTFSI by agarose lower the decomposition speed of perovskite, which obviously increases the power efficiency and stability of device.
关键词： humid stability mechanism,perovskite solar cells,MAPbI3/agarose photoactive composite
更新于2025-11-14 15:24:45
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Aggregation-induced emission (AIE)-active highly emissive novel carbazole-based dyes with various solid-state fluorescence and reversible mechanofluorochromism characteristics
摘要： Three new carbazole-based fluorescent molecules 1-3 functionalized with tetraphenylethene have been successfully synthesized, and these compounds have high thermal stability, and they exhibited different fluorescence in solid states with the superior luminescence quantum yields of 99.04% (1), 98.90% (2) and 39.83% (3). Their aggregation-induced behaviors were explored by the study of photoluminescence spectroscopy. The results showed that luminogens 1-3 exhibited remarkable aggregation-induced emission effect. Furthermore, their distinct mechanical stimulus-responsive fluorescence characteristics were also surveyed by solid-state photoluminescence spectroscopy. Interestingly, the various emitting colors of these luminogens could be changed into the same green, and the repeatabilities of their mechanochromic luminescence behaviors were outstanding, and the powder X-ray diffraction results indicated that the reversible conversion from a crystalline to an amorphous state was responsible for the obvious mechanofluorochromism phenomena of compounds 1-3. This work will be valuable for the exploitation of mechanical-force sensors with typical aggregation-induced emission feature.
关键词： Carbazole,Mechanofluorochromism,Tetraphenylethene,Aggregation-induced emission,Different fluorescence,High thermal stability
更新于2025-11-14 15:23:50
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Flexible and stable organic field-effect transistors using low-temperature solution-processed polyimide gate dielectrics
摘要： Polyimide (PI) has been widely used as a gate dielectric due to its remarkable thermal stability, chemical resistance, and mechanical flexibility. However, the high processing temperature and high surface energy of PI gate dielectrics hinder the realization of flexible and reliable electronic applications with low-cost manufacturing. Here, a low-temperature solution-processed organic field-effect transistor (OFET) is successfully demonstrated using a fully imidized soluble PI gate dielectric. The low temperature processability of soluble PI gate dielectrics is confirmed by investigating the effect of annealing temperature on the dielectric properties and electrical characteristics. By blending 6,13-Bis(triisopropylsilylethynyl)pentacene with polystyrene, the reliability of OFET is considerably enhanced while maintaining high device performance. As a result, OFETs exhibit excellent flexibility and can be integrated with ultrathin parylene substrates without degrading device performance. This work presents the steps to develop flexible and reliable electronic applications with low-cost manufacturing.
关键词： organic field-effect transistors,solution-processed,polyimides,low-temperature,operational stability
更新于2025-11-14 15:19:41
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Suppression of Iodide Ions Migration via Sb2S3 interfacial Modification for stable Inorganic Perovskite Solar Cells
摘要： In mixed halide perovskite, the halide phase segregation is commonly observed due to halide ions migration, which causes severe stability issues in perovskite devices. Here, we directly revealed the iodide-migration process via potentiostatic treatment in CsPbIBr2 perovskite. The absence of iodide ions was reduced significantly via Sb2S3 interfacial modification. We further employed the DFT calculation to optimize the geometry positions at the perovskite interface and radial distribution functions (RDF) to analyze the atom perturbation. The simulation yielded a slight distortion of perovskite lattice at the interface of Sb2S3-CsPbIBr2 and iodide ions fluctuation was reduced due to the decrease of halide vacancies. In addition, the thermally stimulated current was calculated to evaluate the defects density in the modified perovskite device. Due to the Sb2S3 interaction with perovskite, the device became stable against humidity and maintained photoactive over 400 h. The champion efficiency of 9.31% with 26.31% improvement was obtained in modified CsPbIBr2 perovskite solar cells.
关键词： stability,The mixed halide perovskite,Sb2S3,DFT,iodide ions migration
更新于2025-11-14 15:15:56
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A novel orange–red emitting phosphor Sr2LuTaO6:Sm3+ for WLEDs
摘要： A novel double perovskite tantalite orange–red light emitting Sr2LuTaO6:Sm3+ phosphor was synthesized by the solid state reaction. The phase, crystal structure, photoluminescence properties, thermal stability and decay curves were studied. The X-ray diffraction patterns indicated that the phosphor has a pure phase of cubic phase structure. Excited by near-ultraviolet light at 407 nm, the sample exhibited three sharp emission peaks at 564 nm, 600 nm, 645 nm corresponding to the 4G5/2 → 6HJ (J = 5/2, 7/2 and 9/2) transitions, respectively. The optimum doping concentration of Sm3+ ions was determined to be 5 mol% and the concentration quenching process comes from the energy transfer among nearest-neighbor ions. The as-prepared phosphors showed excellent thermal stability, the integral intensity at 423 K is about 91.10% of the initial intensity. The CIE chromaticity coordinates of Sr2LuTaO6:Sm3+ phosphors located in orange–red region. The results suggest that Sr2LuTaO6:Sm3+ phosphors have great potential application in white light-emitting diodes.
关键词： luminescence,thermal stability,white light-emitting diodes,Sr2LuTaO6:Sm3+,phosphor
更新于2025-11-14 15:13:28
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Hole Blocking Layer-Free Perovskite Solar Cells with High Efficiencies and Stabilities by Integrating Subwavelength-Sized Plasmonic Alloy Nanoparticles
摘要： Perovskite solar cells hold great promise as prospective alternatives of renewable power sources. Recently hole blocking layer-free perovskite solar cells, getting rid of complex and high-temperature fabrication processes, have engaged in innovative designs of photovoltaic devices. However, the elimination of the hole blocking layer constrains the energy conversion efficiencies of perovskite solar cells, and severely degrades the stabilities. In this paper a simple approach (without energy-consuming and time-consuming procedures) for the fabrication of hole blocking layer-free perovskite solar cells has been demonstrated by an integration of copper-silver alloy nanoparticles, which are synthesized by wet chemical method with controllable diameters and elemental compositions. The rear-side integration of the subwavelength-sized silver-copper alloy particles (200 nm diameter), through a spraying/drying method, realizes a pronounced absorption enhancement of the perovskite layer by effectively light scattering in a broadband wavelength range, and achieves a series resistance decrease of the solar cell due to high electrical conductivities of the alloy particles. The particle integration achieves the highest efficiency of 18.89% due to the significant improvement in both optical and electrical properties of solar cells, making this device one of the highest-performing blocking layer-free perovskite solar cells and plasmonic perovskite solar cells. Moreover, the copper-based nanoparticles prevent the perovskite from diffusing into metal back electrodes. Because the diffusion can lead to a severe corrosion of the Au electrode and thus an efficiency degradation, the alloy nanoparticle integration between the perovskite and the electrode results in 80% and 200% improvements in the long-term stability and the photostability of solar cells, respectively. Through the proposed simple and effective fabrication process, our results open up new opportunities in the manufacturability of perovskite solar cells.
关键词： light scattering,Perovskite solar cells,plasmonic,subwavelength-sized,alloy,hole blocking layer,stability
更新于2025-10-22 19:40:53
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Improving performance and stability of planar perovskite solar cells through grain boundary passivation with block copolymer
摘要： Organic-inorganic metal halide perovskite solar cells (PSCs) exhibit excellent photovoltaic performance but suffer from instabilities against moisture and heat due to the inherent hydroscopic nature and volatility of their organic components. Herein, we report that employing block copolymer F127 as the passivation reagent in conjunction with solvent annealing process can efficiently improve the performance and stability of corresponding organic-inorganic PSCs. It is anticipated that the hydrophilic poly(ethylene oxide) tails of F127 polymers connect with contiguous perovskite crystals and passivate defects at perovskite grain boundaries, whereas the dangling hydrophobic poly(phenyl oxide) centers suppress perovskite decomposition caused by moisture and heat. After the optimization of the F127 additive, the planar PSCs with champion power conversion efficiencies of 21.01% and 18.71% were achieved on rigid and flexible substrates, respectively. The F127 passivation strategy provides an effective approach for fabricating high-efficiency and stable PSCs.
关键词： flexible solar cells,block copolymer,perovskite solar cells,interface passivation,stability
更新于2025-10-22 19:40:53
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Metamaterial emitter for thermophotovoltaics stable up to 1400?°C
摘要： High temperature stable selective emitters can significantly increase efficiency and radiative power in thermophotovoltaic (TPV) systems. However, optical properties of structured emitters reported so far degrade at temperatures approaching 1200 °C due to various degradation mechanisms. We have realized a 1D structured emitter based on a sputtered W-HfO2 layered metamaterial and demonstrated desired band edge spectral properties at 1400 °C. To the best of our knowledge the temperature of 1400 °C is the highest reported for a structured emitter, so far. The spatial confinement and absence of edges stabilizes the W-HfO2 multilayer system to temperatures unprecedented for other nanoscaled W-structures. Only when this confinement is broken W starts to show the well-known self-diffusion behavior transforming to spherical shaped W-islands. We further show that the oxidation of W by atmospheric oxygen could be prevented by reducing the vacuum pressure below 10?5 mbar. When oxidation is mitigated we observe that the 20 nm spatially confined W films survive temperatures up to 1400 °C. The demonstrated thermal stability is limited by grain growth in HfO2, which leads to a rupture of the W-layers, thus, to a degradation of the multilayer system at 1450 °C.
关键词： W-HfO2 layered structure,selective emitters,metamaterial emitter,high temperature stability,thermophotovoltaics
更新于2025-10-22 19:40:53