Boosting Long-Term Stability of Pure Formamidinium Perovskite Solar Cells by Ambient Air Additive Assisted Fabrication
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ABSTRACT:
SUBMITTER: Salim K
PROVIDER: S-EPMC8506569 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:Compositional engineering has been used to overcome difficulties in fabricating high-quality phase-pure formamidinium perovskite films together with its ambient instability. However, this comes alongside an undesirable increase in bandgap that sacrifices the device photocurrent. Here we report the fabrication of phase-pure formamidinium-lead tri-iodide perovskite films with excellent optoelectronic quality and stability. Incorporation of 1.67?mol% of 2D phenylethylammonium lead iodide into the precursor solution enables the formation of phase-pure formamidinium perovskite with an order of magnitude enhanced photoluminescence lifetime. The 2D perovskite spontaneously forms at grain boundaries to protect the formamidinium perovskite from moisture and suppress ion migration. A stabilized power conversion efficiency (PCE) of 20.64% (certified stabilized PCE of 19.77%) is achieved with a short-circuit current density exceeding 24?mA?cm-2 and an open-circuit voltage of 1.130?V, corresponding to a loss-in-potential of 0.35?V, and significantly enhanced operational stability.
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Project description:This paper presents the results of a combined experimental and analytical/computational study of the effects of pressure on photoconversion efficiencies of perovskite solar cells (PSCs). First, an analytical model is used to predict the effects of pressure on interfacial contact in the multilayered structures of PSCs. The PSCs are then fabricated before applying a range of pressures to the devices to improve their interfacial surface contacts. The results show that the photoconversion efficiencies of PSCs increase by ~40%, for applied pressures between 0 and ~7?MPa. However, the photoconversion efficiencies decrease with increasing pressure beyond ~7?MPa. The implications of the results are discussed for the fabrication of efficient PSCs.
| S-EPMC7188881 | biostudies-literature
Project description:Humidity is known to be inimical to the halide perovskites and thus typically avoided during fabrication. The poor fundamental understanding of chemical interactions between water and the precursors hampers the further development of perovskite fabrication in ambient atmosphere. Here, we disclose a key finding that the ambient water could promote the formation of lead complexes, which when uncontrolled would make their way into large intermediate fibrillar crystallites and thus discontinuous perovskite films unfavorable for photovoltaics among others. To counter this effect, a prenucleation strategy is proposed, which embodies the controlled burst of profuse intermediate nuclei. Consequently, we are able to obtain a compact and uniform perovskite layer, which affords high efficiency perovskite solar cells. More excitingly, the solar cells show high performance uniformity, demonstrating the distinctive advantages of our prenucleation strategy. This work sheds light on developing reliable and cost-effective fabrication methods for industrial production of perovskite solar cells.
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Project description:Poor stability of organic-inorganic halide perovskite materials in humid condition has hindered the success of perovskite solar cells in real applications since controlled atmosphere is required for device fabrication and operation, and there is a lack of effective solutions to this problem until now. Here we report the use of lead (II) thiocyanate (Pb(SCN)2) precursor in preparing perovskite solar cells in ambient air. High-quality CH3NH3PbI3-x(SCN)x perovskite films can be readily prepared even when the relative humidity exceeds 70%. Under optimized processing conditions, we obtain devices with an average power conversion efficiency of 13.49% and the maximum efficiency over 15%. In comparison with typical CH3NH3PbI3-based devices, these solar cells without encapsulation show greatly improved stability in humid air, which is attributed to the incorporation of thiocyanate ions in the crystal lattice. The findings pave a way for realizing efficient and stable perovskite solar cells in ambient atmosphere.
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Project description:Intermediate phase is considered an important aspect to deeply understand the crystallization procedure in the growth of high-quality perovskite layers by an anti-solvent technique. However, the moisture influence on the intermediate phase formation is not clear in air conditions as yet. In this work, pure (FA0.2MA1.8)Pb3X8(DMSO·DMF) intermediate phase was obtained in as-prepared perovskite film by spin-coating the precursor of co-solvent (DMSO and DMF) in an ambient air (RH20-30%). Moreover, the appropriate quantity of ethyl acetate (C4H8O2, EA) also controls the formation of pure intermediate phase. The uniform and homogeneous perovskite film was obtained after annealing this intermediate film. Therefore, the best power conversion efficiency (PCE) of perovskite solar cells (PSCs) is 16.24% with an average PCE of 15.53%, of which almost 86% of its initial PCE was preserved after 30 days in air conditions. Besides, the steady-state output efficiency ups to 15.38% under continuous illumination. In addition, the PCE of large area device (100 mm2) reaches 11.11% with a little hysteresis effect. This work would give an orientation for PSCs production at the commercial level, which could lower the cost of fabricating the high efficiency PSCs.
| S-EPMC6669498 | biostudies-literature
Project description:Formamidinium-lead-iodide (FAPbI3)-based perovskites with bandgap below 1.55?eV are of interest for photovoltaics in view of their close-to-ideal bandgap. Record-performance FAPbI3-based solar cells have relied on fabrication via the sequential-deposition method; however, these devices exhibit unstable output under illumination due to the difficulty of incorporating cesium cations (stabilizer) in sequentially deposited films. Here we devise a perovskite seeding method that efficiently incorporates cesium and beneficially modulates perovskite crystallization. First, perovskite seed crystals are embedded in the PbI2 film. The perovskite seeds serve as cesium sources and act as nuclei to facilitate crystallization during the formation of perovskite. Perovskite films with perovskite seeding growth exhibit a lowered trap density, and the resulting planar solar cells achieve stabilized efficiency of 21.5% with a high open-circuit voltage of 1.13?V and a fill factor that exceeds 80%. The Cs-containing FAPbI3-based devices show a striking improvement in operational stability and retain 60% of their initial efficiency after 140?h operation under one sun illumination.
| S-EPMC5913260 | biostudies-literature
Project description:Formamidinium lead iodide (FAPbI3) is a newly developed hybrid perovskite that potentially can be used in high-efficiency solution-processed solar cells. Here, the temperature-dependent dynamic optical properties of three types of FAPbI3 perovskite films (fabricated using three different precursor systems) are comparatively studied. The time-resolved photoluminescence (PL) spectra reveal that FAPbI3 films made from the new precursor (a mixture of formamidinium iodide and hydrogen lead triiodide) exhibit the longest lifetime of 439 ns at room temperature, suggesting a lower number of defects and lower non-radiative recombination losses compared with FAPbI3 obtained from the other two precursors. From the temperature-dependent PL spectra, a phase transition in the films is clearly observed. Meanwhile, exciton-binding energies of 8.1 and 18 meV for the high- and low-temperature phases are extracted, respectively. Importantly, the PL spectra for all of the samples show a single peak at room temperature, whereas at liquid-helium temperature the emission features two peaks: one in higher energy displaying a fast decay (0.5 ns) and a second red-shifted peak with a decay of up to several microseconds. These two emissions, separated by ~18 meV, are attributed to free excitons and bound excitons with singlet and triplet characters, respectively.
| S-EPMC6059954 | biostudies-literature
Project description:Perovskite solar cells (PSCs) have achieved extremely high power conversion efficiencies (PCEs) of over 25%, but practical application still requires further improvement in the long-term stability of the device. Herein, we present an in situ interfacial contact passivation strategy to reduce the interfacial defects and extraction losses between the hole transporting layer and perovskite. The existence of PbS promotes the crystallization of perovskite, passivates the interface and grain boundary defects, and reduces the nonradiation recombination, thereby leading to a champion PCE of 21.07% with reduced hysteresis, which is one of the best results for the methylammonium (MA)-free, cesium formamidinium double-cation lead-based PSCs. Moreover, the unencapsulated device retains more than 93% and 82% of its original efficiencies after 1 year's storage under ambient conditions and thermal aging at 85°C for 1,000 h in a nitrogen atmosphere, likely due to the usage of MA-free perovskite and the enhanced surface hydrophobicity.
| S-EPMC6992903 | biostudies-literature
Project description:While there is great demand for effective, affordable radiation detectors in various applications, many commonly used scintillators have major drawbacks. Conventional inorganic scintillators have a fixed emission wavelength and require expensive, high-temperature synthesis; plastic scintillators, while fast, inexpensive, and robust, have low atomic numbers, limiting their X-ray stopping power. Formamidinium lead halide perovskite nanocrystals show promise as scintillators due to their high X-ray attenuation coefficient and bright luminescence. Here, we used a room-temperature, solution-growth method to produce mixed-halide FAPbX3 (X = Cl, Br) nanocrystals with emission wavelengths that can be varied between 403 and 531 nm via adjustments to the halide ratio. The substitution of bromine for increasing amounts of chlorine resulted in violet emission with faster lifetimes, while larger proportions of bromine resulted in green emission with increased luminescence intensity. By loading FAPbBr3 nanocrystals into a PVT-based plastic scintillator matrix, we produced 1 mm-thick nanocomposite scintillators, which have brighter luminescence than the PVT-based plastic scintillator alone. While nanocomposites such as these are often opaque due to optical scattering from aggregates of the nanoparticles, we used a surface modification technique to improve transmission through the composites. A composite of FAPbBr3 nanocrystals encapsulated in inert PMMA produced even stronger luminescence, with intensity 3.8× greater than a comparative FAPbBr3/plastic scintillator composite. However, the luminescence decay time of the FAPbBr3/PMMA composite was more than 3× slower than that of the FAPbBr3/plastic scintillator composite. We also demonstrate the potential of these lead halide perovskite nanocomposite scintillators for low-cost X-ray imaging applications.
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Project description:All-inorganic CsPbX3-based perovskites, such as CsPbI2Br, show much better thermal and illumination stability than their organic-inorganic hybrid counterparts. However, fabrication of high-quality CsPbI2Br perovskite film normally requires annealing at a high temperature (>250 °C) that is not compatible with the plastic substrate. In this work, a Lewis base adduct-promoted growth process that makes it possible to fabricate high quality CsPbI2Br perovskite films at low temperature is promoted. The mechanism is attributed to synthesized dimethyl sulfoxide (DMSO) adducts which allow a low activation energy route to form CsPbI2Br perovskite films during the thermal annealing treatment. A power conversion efficiency (PCE) of 13.54% is achieved. As far as it is known, this is the highest efficiency for the CsPbI2Br solar cells fabricated at low temperature (120 °C). In addition, the method enables fabrication of flexible CsPbI2Br PSCs with PCE as high as 11.73%. Surprisingly, the bare devices without any encapsulation maintain 70% of their original PCEs after being stored in ambient air for 700 h. This work provides an approach for preparing other high performance CsPbX3-based perovskite solar cells (PSCs) at low temperature, particularly for flexible ones.
| S-EPMC6247060 | biostudies-literature