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Solvent Engineering Using a Volatile Solid for Highly Efficient and Stable Perovskite Solar Cells
摘要： A strategy for efficaciously regulating perovskite crystallinity is proposed by using a volatile solid glycolic acid (HOCH2COOH, GA) in an FA0.85MA0.15PbI3 (FA: HC(NH2)2; MA: CH3NH3) perovskite precursor solution that is different from the common additive approach. Accompanied with the first dimethyl sulfoxide sublimation process, the subsequent sublimation of GA before 150 °C in the FA0.85MA0.15PbI3 perovskite film can artfully regulate the perovskite crystallinity without any residual after annealing. The improved film formation upon GA modification induced by the strong interaction between GA and Pb2+ delivers a champion power conversion efficiency (PCE) as high as 21.32%. In order to investigate the role of volatility in perovskite solar cells (PSCs), nonvolatile thioglycolic acid (HSCH2COOH, TGA) with a similar structure to GA is utilized as an additive reference. Large perovskite grains are obtained by TGA modification but with obvious pinholes, which directly leads to an increased defect density accompanied by a decline in PCE. Encouragingly, the champion PCE achieved for GA-based PSC device (21.32%) is almost 13% or 20% higher than those of the control device or TGA-based device. In addition, GA-modified PSCs exhibit the best stability in light-, thermal-, and humidity-based tests due to the improved film formation.
关键词： pinholes,solvent engineering,volatile,crystal growth,perovskite solar cells
更新于2025-09-19 17:13:59
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Solvent engineering of LiTFSI towards high-efficiency planar perovskite solar cells
摘要： The performance and stability of perovskite solar cell (PSC) are inseparable from the quality of perovskite film, and the solvent engineering is being seemed as an effective strategy to enhance the properties of perovskite. Acetonitrile (ACN) is often used as a solvent to dissolve bis(trifluoromethane)sulfonimide lithium salt (LiTFSI), but ACN can corrode the perovskite film, which hinders the promotion of PSC efficiency and durability. Herein, a solvent engineering approach is implemented to search for suitable alternatives for ACN to abate the degradation of the perovskite films. The results demonstrate that isopropanol (IPA) with smaller polarity can effectively dissolve LiTFSI and slow down the degradation of the perovskite layer compared with ACN, which can result in the reduction of defects as well as the nonradiative recombination. Consequently, the devices using LiTFSI/IPA as additive achieve superior power conversion efficiencies (PCEs) with relatively less hysteresis effects and get a champion PCE of 19.43%, while the device using LiTFSI/ACN gets an inferior PCE of 17.12%.
关键词： Trap density,Nonradiative recombination,Solvent engineering,Isopropanol,Perovskite solar cells
更新于2025-09-16 10:30:52
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Performance data of CH3NH3PbI3 Inverted Planar Perovskite Solar Cells via Ammonium Halide Additives
摘要： The data provided in this data set is the study of organic-inorganic hybrid perovskite solar cells fabricated through incorporating the small amounts of ammonium halide NH4X (X=F, Cl, Br, I) additives into a CH3NH3PbI3 (MAPbI3) perovskite solution and is published as “High-Performance CH3NH3PbI3 Inverted Planar Perovskite Solar Cells via Ammonium Halide Additives”, available in Journal of Industrial and Engineering Chemistry [1]. A compact and uniform perovskite absorber layer with large perovskite crystalline grains, is realized by simply incorporating small amounts of additives into precursor solutions, and utilizing the anti-solvent engineering technique to control the nucleation and growth of perovskite crystal, turning out the enhanced device efficiency (NH4F: 14.88 ± 0.33 %, NH4Cl: 16.63 ± 0.21 %, NH4Br: 16.64 ± 0.35 %, and NH4I: 17.28 ± 0.15 %) compared to that of a reference MAPbI3 device (Ref.: 12.95 ± 0.48 %). In addition, this simple technique of ammonium halide addition to precursor solutions increase the device reproducibility as well as long term stability.
关键词： perovskite grain size,inverted planar structure,CH3NH3PbI3 perovskite,ammonium halide additives,anti-solvent engineering
更新于2025-09-16 10:30:52
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Pre-crystallisation applied in sequential deposition approaches to improve the photovoltaic performance of perovskite solar cells
摘要： The fabrication process for perovskite films is critical for their microstructure and photo-electrical properties. In this study, a pre-preparation step for perovskite crystal particles with a conventional two step spin-coating method was introduced for improving the quality of the prepared perovskite films. By adding CH3NH3I into the PbI2 precursor solution and performing anti-solvent extraction during the preparation process, a small amount of perovskite crystal particles was produced in the PbI2 layers. We demonstrated that the pre-preparation of perovskite crystal particles enhanced the grain size and coverage of the perovskite films due to modification of the surface morphology and crystallisation of the PbI2 layers. Furthermore, after optimisation, the crystal size in the perovskite films reached almost 3 μm, which tremendously enhanced the generation and transportation of photo-generated carriers in photo-voltaic devices. Under illumination, the fill factor (FF) and short circuit current density (Jsc) of the corresponding devices increased, and the photoelectric conversion efficiency (PCE) was enhanced from 11.7% to 17.5%. Further, the stability of the devices in dark humid air was improved. Our results demonstrate that pre-preparing the perovskite crystal particles is useful for the fabrication of high-quality perovskite films. This approach can also be applied to devices based on perovskite films with other compositions.
关键词： Solvent engineering,sequential,solar cells,Crystallization,perovskite,deposition
更新于2025-09-12 10:27:22
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Ultrafast THz photophysics of solvent engineered triple-cation halide perovskites
摘要： Solution processed thin film organic-inorganic perovskites are key to the large scale manufacturing of next generation wafer scale solar cell devices. The high efficiency of the hybrid perovskite solar cells is derived mainly from the large carrier mobility and the charge dynamics of films, which heavily depend on the type of solvent used for the material preparation. Here, we investigate the nature of conduction and charge carrier dynamics of mixed organic-inorganic cations [methylammonium (MA), formamidinium (FA), and cesium (Cs)] along with the mixed halides [iodine (I) and bromine (Br)] perovskite material [Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3] synthesized in different solvents using optical pump terahertz probe (OPTP) spectroscopy. Our findings reveal that carrier mobilities and diffusion lengths strongly depend on the type of solvent used for the preparation of the mixed cation perovskite film. The mixed cation perovskite film prepared using dimethylformamide/dimethylsulfoxide solvent shows greater mobility and diffusion length compared to γ-butyrolactone solvent. Our findings provide valuable insights to improve the charge carrier transport in mixed cation perovskites through solvent engineering.
关键词： charge carrier dynamics,OPTP spectroscopy,diffusion length,perovskites,carrier mobility,solvent engineering
更新于2025-09-09 09:28:46