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- 实验方案
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Transparent, flexible MAPbI3 perovskite microwire array passivated with ultra-hydrophobic supramolecular assembly for stable and high-performance photodetectors
摘要： The emergence of organic-inorganic hybrid perovskites (OHPs) has revolutionised the potential performance of optoelectronic devices, most perovskites are opaque and hence incompatible with transparent optoelectronics, and sensitive to environmental degradation. Here, a single-step fabrication of ultra-long MAPbI3 perovskite microwire array over a large-area using stencil lithography based on a sequential vacuum sublimation. The environmental stability of MAPbI3 is empowered a newly designed and synthesized transparent supramolecular self-assembly, based on a mixture of two tripodal L-Phe-C11H23/C7F15 molecules, which showed a contact angle of 105° and served as ultra-hydrophobic passivation layer for more than 45 days in ambient atmosphere. The MAPbI3 microwire array passivated with supramolecular self-assembly demonstrate for the first time both excellent transparency of ~89% at 550 nm and remarkable photoresponse with photo-switching ratio of ~104, responsivity of 789 A/W, detectivity of 1014 Jones, linear dynamic range of ~ 122 dB, and rise time of 432 μs. Furthermore, the photodetector fabricated on flexible PET substrate demonstrated robust mechanical flexibility even beyond 1200 bending cycles. Therefore, the scalable stencil lithography and supramolecular passivation approaches have the potential to deliver next-generation transparent, flexible, and stable optoelectronics.
关键词： transparency,stencil lithography,photodetectors,MAPbI3,supramolecular self-assembly,flexibility,organic-inorganic hybrid perovskites,environmental stability
更新于2025-09-23 15:21:01
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Controlling films structure by regulating 2D Ruddlesden-Popper perovskite formation enthalpy for efficient and stable tri-cation perovskite solar cells
摘要： The incorporation of bulky organic cations to metal-halide perovskites, forming the 2D-3D heterojunctions, has dramatically improved the stability of perovskite solar cells (PSCs). Nevertheless, the power conversion efficiencies (PCEs) of these PSCs are typically sacrificed because the formed 2D structures possess larger dielectric confinement, wider bandgaps, higher exciton binding energies and lower charge-carrier mobilities than the 3D perovskites. Here, we demonstrate that the environmental stability of the PSCs could be significantly improved without sacrificing the efficiency by introducing hydrophobic polyfluorinated cations (CF3CF2CH2NH3+, 5F-PA+) to the metal-halide perovskites. Due to the large 2D perovskite formation enthalpy with polyfluorinated cations, the addition of such cations will form a protective layer at the grain boundaries of 3D perovskite rather than form the 2D perovskites. The resultant solar cells based on 5F-PA0.05[Cs0.05(MA0.17FA0.83)0.95]0.95Pb(Br0.17I0.83)3 exhibit a substantially increased PCE of 22.86% compared with that (20.69%) of the control Cs0.05(MA0.17FA0.83)0.95Pb(Br0.17I0.83)3 devices. More importantly, the optimized devices could keep 80% of their original PCEs after >3000 h in ambient environment with 65 ± 10% relative humidity, which is attributed to hydrophobic fluorine moieties.
关键词： power conversion efficiency,perovskite solar cells,environmental stability,polyfluorinated cations,2D-3D heterojunctions
更新于2025-09-23 15:19:57
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Highly efficient organic photovoltaics with enhanced stability through the formation of doping-induced stable interfaces
摘要： Flexible organic photovoltaics (OPVs) are promising power sources for wearable electronics. However, it is challenging to simultaneously achieve high efficiency as well as good stability under various stresses. Herein, we demonstrate the fabrication of highly efficient (efficiency, 13.2%) and stable OPVs based on nonfullerene blends by a single-step postannealing treatment. The device performance decreases dramatically after annealing at 90 °C and is fully recovered after annealing at 150 °C. Glass-encapsulated annealed OPVs show good environmental stability with 4.8% loss in efficiency after 4,736 h and an estimated T80 lifetime (80% of the initial power conversion efficiency) of over 20,750 h in the dark under ambient condition and T80 lifetime of 1,050 h at 85 °C and 30% relative humidity. This environmental stability is enabled by the synergetic effect of the stable morphology of donor/acceptor blends and thermally stabilized interfaces due to doping. Furthermore, the high efficiency and good stability are almost 100% retained in ultraflexible OPVs and minimodules which are mechanically robust and have long-term operation capability and thus are promising for future self-powered and wearable electronics.
关键词： nonfullerene acceptor,environmental stability,ultraflexible devices,organic photovoltaics,high efficiency
更新于2025-09-19 17:13:59
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Development of flexible, stable, and efficient inverted organic solar cells harvesting light in all directions
摘要： In this work, we designed low-cost, liquid-free, efficient, and highly flexible fiber-shaped inverted structure organic solar cells (FOSCs) over a flexible polyethylene terephthalate (PET) monofilament substrate. We also prepared a graphene–ZnO (G-ZnO) composite, wherein G sheets were compacted into a bunched-up structure through the binding force of Zn atoms with the C atoms of G. This composite was then utilized as a bifunctional layer i.e. electron transport and downconversion spectral in the FOSCs. The FOSCs based on the G-ZnO (D-1) demonstrated a power conversion efficiency (PCE) of 2.13% out of which 4.89% and 5% was retained after 8000 times bending and 120 h storage in ambient environmental conditions, respectively. The non-G-ZnO FOSCs (D-2) demonstrated a PCE of 1.78% and retained 5% and 6% of the initial value after 6000 bends and 48h of storage in ambient environmental conditions, respectively. This better performance of D-1 compared to that of D-2 is due to the interfacial functionalization of G-sheets and ZnO nanoparticles inside the G-ZnO composite. Because of these interfacial chemical bonds, the G sheets were in close contact with each other and attached firmly through the ZnO molecules. As a result, these compacted G layers could serve as a strong barrier resisting the penetration of water molecules inside the device, thereby leading to an improved lifetime for the device. Additionally, the longitudinal and cross linkage of G-sheets could improve the mechanical properties of the G-ZnO composite, which in turn enhanced the flexibility of D-1. Finally, these interface functionalizations could work as linking bridges, providing an additional pathway for the transportation of free charge carriers. Therefore, D-1 demonstrated a higher Jsc by collecting a greater number of charges at the electrode compared to D-2, because the latter lacked similar functionalization.
关键词： Electron transport layer,Mechanical and Environmental stability,G-ZnO interface chemistry,Downconversion spectral,Fiber-shaped OSCs
更新于2025-09-16 10:30:52
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Regulated Crystallization of Efficient and Stable Tin-based Perovskite Solar Cells via Self-sealing Polymer
摘要： Tin-based perovskite solar cells (PVSCs) have emerged as the most promising lead-free perovskite materials owing to their superior optoelectronic properties. However, the deficiency of accurate control for the tin-based perovskite crystallization process increases the possibility of unexpected perovskite film morphology and defects, resulting in inferior power conversion efficiency (PCE). Meanwhile, the poor environmental stability of tin-based perovskite film hinders its further development. In this work, a unique polymer [poly(ethylene-co-vinyl acetate) (EVA)] is introduced into anti-solvent during spin coating of formamidinium tin tri-iodide (FASnI3) precursor solution. The C=O groups contained in EVA have a powerful Lewis acid-base complexation with uncoordinated tin atoms in perovskite grains, which can greatly improve grain size, optimize grain orientation and decrease surface defects of FASnI3 films. This strategy offers an impressive PCE of 7.72% with favorable reproducibility. More importantly, the PVSCs devices based on FASnI3-EVA absorber have a self-encapsulation effect, which exhibits distinguished moisture and oxygen barrier property, thereby retaining 62.4% of the original efficiency value after aging for 48 h in air environment with humidity of 60%. Such convenient strategy provides a new inspiration for the establishment of stable and high performance tin-based PVSCs.
关键词： environmental stability,self-encapsulation,poly(ethylene-co-vinyl acetate),crystallization,tin-based perovskite solar cells
更新于2025-09-16 10:30:52
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Alkaline-Earth Bis(trifluoromethanesulfonimide) Additives for Efficient and Stable Perovskite Solar Cells
摘要： Environmental instability of Spiro-OMeTAD-based hole transport layer (HTL) caused due to rapid aggregation and hydration of its additive, Lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI), gives rise to an accelerated degradation of the resulting perovskite solar cells (PSCs). Herein, we show that replacing the Li-TFSI with the more hydrophobic alkaline-earth bis(trifluoromethanesulfonyl)imide additives, namely Mg-TFSI2 and Ca-TFSI2, can effectively stabilize the coordination complexes between the TFSI-salts and 4-tert-Butylpyridine, which in turn results in retarded additive aggregation and hydration, enabling enhanced moisture-resistance of the subsequent HTLs. Moreover, by manipulating this substitution method, we achieved high-quality HTLs with increased hole mobility, better-formed interface with the adjacent perovskite, allowing improved hole extraction process. Incorporating these HTLs into photovoltaic devices, we obtained a substantial performance improvement, with the champion PSC yielded a power conversion efficiency of over 20%. In addition, un-encapsulated devices stabilized by the alkaline-earth bis(trifluoromethanesulfonyl)imide additive maintained 83% its initial efficiency for 193 days after aging in ambient air (RH% = 55-70%).
关键词： Perovskite solar cells,4-tert-Butylpyridine,environmental stability,alkaline-earth bis(trifluoromethanesulfonimide),hole transport layer,charge transfer
更新于2025-09-12 10:27:22
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1D Pyrrolidinium Lead Iodide for Efficient and Stable Perovskite Solar Cells
摘要： Due to the superior environmental stability, the utilization of low-dimensional perovskites in organometal halide solar cells (OMHSCs) has been on the sharp increase. Herein, we report a method to in situ form one-dimensional pyrrolidinium lead iodide (1D PyPbI3) atop the photoactive three-dimensional methylammonium lead iodide (3D MAPbI3) using pyrrolidine post-treatment. As compared to the 3D MAPbI3, the 1D PyPbI3 has a wider bandgap and is more environmentally stable, which serves as a tunnelling contact to mitigate charge carrier recombination and robust barrier against environmental degradation when incorporated into OMHSCs. Accordingly, power conversion efficiencies of the resulting MAPbI3 devices were enhanced from an average of 14.86 ± 0.65% to 15.9 ± 0.58% while shelf-life stability was significantly prolonged.
关键词： perovskite solar cell,one-dimensional perovskite,environmental stability,pyrrolidine,photovoltaic performance,pyrrolidinium lead iodide,charge recombination
更新于2025-09-11 14:15:04
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Solution-Processed Inorganic Perovskite Flexible Photodetectors with High Performance
摘要： All inorganic CsPbI3-xBrx perovskites have been widely used in photodetectors due to their excellent optoelectronic properties and simple preparation processes. Here, high-performance flexible photodetectors based on inorganic CsPbI3-xBrx perovskites are demonstrated, which are achieved by a modified solution-processed method. When biased at a low voltage of 10 mV, the device yielded fast response speeds (90 μs /110 μs for CsPbI2Br PDs and 100 μs/140 μs for CsPbIBr2 PDs), a high on/off ratio of 104, and a high detectivity about 1012 Jones. Meanwhile, the devices showed outstanding environmental stability and mechanical flexibility. The periodic I-t curves had negligible fluctuation (< 5%) after storing in air atmosphere for 30 days or bending for 100 times. The results indicate that CsPbI3-xBrx perovskites have great potential in photodetection areas and pave the way to achieve high-performance flexible PDs.
关键词： Mechanical flexibility,Environmental stability,Low bias voltage,CsPbI3-xBrx-based flexible PDs
更新于2025-09-11 14:15:04