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Formamidinium-cesium lead triiodide (FACsPbI) perovskite holds great promise for perovskite solar cells (PSCs) with both high efficiency and stability. However, the defective perovskite surfaces induced by defects and residual tensile strain largely limit the photovoltaic performance of the corresponding devices. Here, the passivation capability of alkylamine-modified pyridine derivatives for the surface defects of FACsPbI perovskite is systematically studied. Among the studied surface passivators, 3-(2-aminoethyl)pyridine (3-PyEA) with the suitable size is demonstrated to be the most effective in reducing surface iodine impurities and defects (V and I) through its strong coordination with N. Additionally, the tail amino group (─NH) from 3-PyEA can react with FA cations to reduce the surface roughness of perovskite films, and the reaction products can also passivate FA vacancies (V), and further strengthen their binding interaction to perovskite surfaces. These merits lead to suppressed nonradiative recombination loss, the release of residual tensile stress for the perovskite films, and a favorable energy-level alignment at the perovskite/[6,6]-phenyl-C-butyric acid methyl ester interface. Consequently, the resulting inverted FACsPbI PSCs obtain an impressive power conversion efficiency (PCE) of 25.65% (certified 25.45%, certified steady-state efficiency 25.06%), along with retaining 96.5% of the initial PCE after 1800 h of 1-sun operation at 55 °C in air.
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http://dx.doi.org/10.1002/adma.202415100 | DOI Listing |
Cell Mol Biol (Noisy-le-grand)
September 2025
Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Despite significant advancements in the treatment of non-small cell lung cancer (NSCLC) using conventional therapeutic methods, drug resistance remains a major factor contributing to disease recurrence. In this study, we aimed to explore the potential benefits of combining PI3K inhibition with Cisplatin in the context of NSCLC-derived A549 cells. Human non-small cell lung cancer A549 cells were cultured and treated with BKM120, cisplatin, or their combination.
View Article and Find Full Text PDFJ Med Chem
September 2025
Applied Pharmaceutical Science, Inc., Building 10-1, No.2, Jingyuan North Street, BDA, Beijing 100176, China.
This study reports the discovery and preclinical activity of APS03118, a novel selective RET inhibitor featuring a novel tricyclic pyrazolo[3',4':3,4]pyrazolo[1,5-]pyridine hinge-binding scaffold designed to overcome acquired resistance to first-generation selective RET inhibitors (SRIs). By enhancing hydrogen bonding with conserved hinge residues (Glu805, Ala807), APS03118 potently inhibits wild-type RET and diverse resistance mutations, including solvent-front (G810R/S/C), gatekeeper (V804M/L/E), roof (L730I/M), and hinge (Y806C/N/H) variants. In preclinical models, APS03118 induced complete tumor regression in KIF5B-RET and CCDC6-RET V804 M patient-derived xenografts (PDXs) and significantly prolonged survival in an intracranial CCDC6-RET metastasis model.
View Article and Find Full Text PDFOrg Lett
September 2025
Department of Chemistry, University of Calcutta, 92 A. P. C. Road, Kolkata-700009, India.
This study introduces microwave-assisted, Fe(III)-catalyzed ring-opening annulations of isoxazoles, enabling the rapid and selective synthesis of 1,4-diacyl pyrroles and substituted pyridines. By leveraging microwave irradiation and transition metal catalysis, this approach enhances the reaction efficiency, reduces reaction times, and promotes high regioselectivity under mild conditions. Under thermal conditions, the Ru(II) catalyst led to the synthesis of nicotinamide derivatives.
View Article and Find Full Text PDFRSC Adv
August 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research-Raebareli (NIPER-R) Lucknow UP 226002 India +91-522-2975587 +91-522-2499703.
This paper presents a metal-free synthetic protocol for assembling novel benzofuro[2,3-]pyridin-3-ols (BFPYOLs) using 2,3-disubstituted benzofuran derivatives with good yield. The method's advantages include the absence of an expensive metal catalyst, organic ligands, and easily accessible starting materials. The photophysical properties of the synthesized BFPYOLs are investigated, revealing that the largest is displayed by compound 7g at 389 nm, while the largest is observed in compound 7i at 494 nm in DMSO solvent.
View Article and Find Full Text PDFAnal Chim Acta
November 2025
School of Materials Science and Engineering, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, China. Electronic address:
Background: Bisulfite (HSO) plays crucial roles in food safety and physiological health. In the food industry, sulfur dioxide (SO) and its derivative bisulfite (HSO) are extensively employed as preservatives and bleaching agents. Nonetheless, overconsumption of bisulfite can present health hazards like asthma and potentially cancer.
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