Rational molecular design and suitable device engineering are two important strategies to boost the efficiencies in organic solar cells (OSCs). Yet these two approaches are independently developed, while their synergy is believed to be more productive. Herein, a branched polyfluoride moiety, heptafluoroisopropoxyl group, is introduced into the side chains of conjugated polymers for the first time. Compared with the conventional alkyl chain, this polyfluoride chain can endow the resulting polymer namely PF7 with highly packing order and strong crystallinity owing to the strong polarization and fluorine-induced interactions, while good solubility and moderate miscibility are retained. As a result, PF7 comprehensively outperforms the state-of-the-art polymer PM6 in photovoltaic properties. More importantly, based on the solubility of heptafluoroisopropoxyl groups in fluorous solvents, a new post-treatment denoted as fluorous solvent vapor annealing (FSVA) is proposed to match PF7. Differing from the existing post-treatments, FSVA can selectively reorganize fluoropolymer molecules but less impact small molecules in blend films. By employing the synergy of fluoropolymer and fluorous solvent, the device achieves a remarkable efficiency of 19.09%, which is among the best efficiencies in binary OSCs. The polymer PF7 and the FSVA treatment exhibit excellent universality in various OSCs with different material combinations or device architectures.
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http://dx.doi.org/10.1002/adma.202404824 | DOI Listing |
Nat Commun
November 2024
Department of Materials Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Nanoporous solids, including metal-organic frameworks (MOFs), have long been known to capture small molecules by adsorption on their pore surfaces. Liquids are also known to accommodate small molecules by dissolution. These two processes have been recognized as fundamentally distinct phenomena because of the different nature of the medium-solids and liquids.
View Article and Find Full Text PDFChemSusChem
November 2024
State Key Laboratory of Elemento-organic Chemistry, College of Chemistry, Nankai University, Weijin Road No. 94, Tianjin, 300071, China.
Chem Pharm Bull (Tokyo)
October 2024
School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.
As an easy-to-handle reagent for the in situ generation of outstandingly electrophilic TfC=CH (Tf=CFSO), we have designed and synthesised a novel 4-substituted 2-fluoropyridinium zwitterion, in which a partially fluorinated alkyl group is attached to the pyridinium 4-position. Its zwitterionic nature has been well characterised by quantum chemical bonding analysis. By using this reagent, a wide variety of organic compounds, including commercial bioactive agents, were successfully decorated by the strongly acidic or ionic functionality.
View Article and Find Full Text PDFJ Sep Sci
August 2024
Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
In this study, we focused on the fluorous affinity acting among fluorine compounds, and then developed a new separation medium and evaluated their performance. We prepared the stationary phases for a column using silica gel-modified alkyl fluoride and investigated the characteristics of fluorous affinity by comparing them with a typical stationary phase, which does not contain fluorine, using high-performance liquid chromatography (HPLC). In HPLC measurements, we confirmed that while all non-fluorine compounds were not retained, retention of fluorine compounds increased as the number of fluorine increased with the stationary phase.
View Article and Find Full Text PDFJ Phys Chem B
August 2024
Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
Due to the inherent high electronegativity of fluorine, perfluorocarbons have the potential to exhibit unusual characteristics. Fluorous solvents, in this context, may afford an anomalous solubilizing behavior compared to their hydrocarbon analogues. Addition of perfluorodecalin (PFD) to -hexane results in unusual fluorescence quenching of polycyclic aromatic hydrocarbons (PAHs) by the quencher nitromethane.
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