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Formamidinium lead triiodide (FAPbI) has received significant attention in the field of perovskite solar cells (PSCs) owing to its excellent optoelectronic properties and high thermal stability. However, the photoactive α-FAPbI perovskites are highly susceptible to degradation into non-perovskite δ-FAPbI phases, especially under humid conditions, which severely diminishes the device performance of FAPbI PSCs. Here, we propose an interfacial seeding strategy for regulating crystallization and stabilizing α-FAPbI perovskites in humid air. By post-treating an antisolvent-free, air-processed perovskite wet film with inorganic cesium lead triiodide (CsPbI) nanocrystals, a functional seed layer is formed that effectively mitigates the erosion by humid air while facilitating the conversion of intermediates to the α-FAPbI phase. The interfacial seed-modified FAPbI perovskite films exhibit improved crystal quality and denser morphology. As a result, the efficiency of all-air-processed carbon-based PSCs is improved from 15.90% for the control to 18.04%. In addition, the unencapsulated PSCs based on interfacial seed-modified FAPbI films show improved environmental stability compared to their control counterparts, maintaining 80% of their initial efficiency after 60 days.
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http://dx.doi.org/10.1039/d4dt03120b | DOI Listing |
J Phys Chem Lett
September 2025
Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87106, United States.
Defects significantly influence charge transport in CHNHPbI (MAPbI) perovskite solar cells, particularly at interfaces. Using quantum dynamics simulation, we reveal a distinct interstitial iodine (I) defect behavior at different positions in the TiO/MAPbI system. In the perovskite bulk-like region, I exhibits high mobility and dissociates detrimental iodine trimers, facilitating small-to-large polaron transition and promoting shallow trap formation.
View Article and Find Full Text PDFRSC Adv
September 2025
School of Engineering and Technology, National Textile University 37640 Faisalabad Pakistan
[This retracts the article DOI: 10.1039/D4RA01544D.].
View Article and Find Full Text PDFNanomicro Lett
September 2025
College of New Materials and New Energies, Shenzhen Technology University, Lantian Road 3002, Pingshan, 518118, Shenzhen, People's Republic of China.
The introduction of two-dimensional (2D) perovskite layers on top of three-dimensional (3D) perovskite films enhances the performance and stability of perovskite solar cells (PSCs). However, the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results. In this study, we compared two fluorinated salts: 4-(trifluoromethyl) benzamidine hydrochloride (4TF-BA·HCl) and 4-fluorobenzamidine hydrochloride (4F-BA·HCl) to engineer the 3D/2D perovskite films.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Quantum Chemistry Division, Yokohama City University, Seto 22-2, Kanazawa-Ku, Yokohama 236-0027, Kanagawa, Japan.
Perovskite-silicon tandem solar cells have attracted considerable attention owing to their high power conversion efficiency (PCE), which exceeds the limits of single-junction devices. This study focused on lead-free tin-based perovskites with iodine-bromine mixed anions. Bromide perovskites have a wide bandgap; therefore, they are promising light absorbers for perovskite-silicon tandem solar cells.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Perovskite materials have revolutionized optoelectronics by virtue of their tunable bandgaps, exceptional optoelectronic properties, and structural flexibility. Notably, the state-of-the-art performance of perovskite solar cells has reached 27%, making perovskite materials a promising candidate for next-generation photovoltaic technology. Although numerous reviews regarding perovskite materials have been published, the existing reviews generally focus on individual material systems (e.
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