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Rapid fabrication of perovskite solar cells through intense pulse light annealing of SnO2 and triple cation perovskite thin films
摘要： Rapid evolution of perovskite solar cells (PSCs) performance and stability has inclined the research focus towards scalable bulk fabrication through high speed and cost-effective automated methods. For the first time, intense pulsed light (IPL) is utilized to rapidly fabricate efficient PSCs through swift annealing of both the SnO2 electron transport layer (ETL) and mixed triple cation perovskite thin films. The addition of di-iodomethane (CH2I2) alkyl-halide could enhance the PSC efficiency by retarding the crystallization and improving the surface morphology of the perovskite photoactive film through supplying iodine cleaved by ultraviolet energy during IPL process. The maximum efficiency and fill factor of the PSCs fabricated by IPL annealing were 12.56% and 78.3% for the rigid glass-FTO slides, and 7.6% and 64.75% for flexible PET-ITO substrates when processed in the ambient with relative humidity of 60%, respectively. The annealed materials were characterized through Scanning electron microscopy (SEM), UV-vis, photoluminescence (PL), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) techniques. In addition, impedance spectroscopy (IS) and current-voltage measurements were conducted to study the functionality of fabricated cells. Our results delineated the feasibility of sequential step IPL annealing on rapid fabrication of efficient PSCs which is directly applicable for scalable roll-to-roll manufacturing.
关键词： Di-iodomethane,SnO2,Rapid thermal annealing,Intense pulse light,Perovskite solar cell
更新于2025-09-16 10:30:52
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State-Resolved Probing of Attosecond Timescale Molecular Dipoles
摘要： We report an experimental study of iodomethane attosecond transient absorption spectroscopy (ATAS) in the region of iodine 4d core-to-valence/Rydberg excitation. Similar to previous atomic experiments, XUV-NIR delay-dependent absorbance changes reflect a light-induced phase due to an NIR-field driven AC Stark shift of the excited states, as well as pathway interferences arising from couplings between neighboring states. As a novel aspect of molecular ATAS, we observe pronounced differences between the ATAS signatures of valence and Rydberg states. While the core-to-valence transitions carry the majority of the XUV oscillator strength, the core-to-Rydberg transitions are dominantly affected by a moderately strong, non-ionizing NIR field. Our experimental findings are corroborated by ab-initio calculations and ATAS simulations.
关键词： core-to-valence,attosecond transient absorption spectroscopy,iodomethane,core-to-Rydberg,AC Stark shift,ab-initio calculations,XUV-NIR
更新于2025-09-04 15:30:14