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The invention of near-infrared pedant-based double-cable conjugated polymers has demonstrated remarkable efficacy in single-component organic solar cells (SCOSCs). This work focuses on the innovative double-cable conjugated polymers aimed at attaining good absorption and suitable energy levels. Specifically, in the aromatic side units, the electron-donating (D) part is designed using a thieno[3,4-]pyrrole-4,6-dione (TPD) as a core unit, flanked by two cyclopentadithiophene groups on either side. The electron-deficient (A) terminal groups consist of 2-(3-oxo-2,3-dihydro-1-cyclopenta[]naphthalen-1-ylidene) malononitrile (NC), which can be further modified through fluorination to modulate the physical properties and packing modes of the acceptor material. The resulting double-cable conjugated polymers exhibit broad absorption spectra spanning 500-850 nm and possess lowered Frontier energy levels when incorporating fluorine elements, providing decreased voltage losses in SCOSCs. Therefore, SCOSCs fabricated using these polymers have demonstrated power conversion efficiencies ranging from 7.6 to 10.2%, in which fluorine-containing double-cable conjugated polymers showed higher PCEs due to more favorable crystalline packing, enhanced exciton dissociation probability, and charge-transporting ability.
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http://dx.doi.org/10.1021/acsami.3c09528 | DOI Listing |
ACS Appl Mater Interfaces
May 2025
Department of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering (SBASSE), Lahore University of Management Sciences (LUMS), Lahore 54792, Pakistan.
Photocatalytic production of hydrogen peroxide (HO) is being extensively explored as a cleaner route to one of the most consumed oxidants. In this context, precisely designed organic semiconductor polymers have only recently been recognized as promising photocatalysts. Contributing to this emerging area, herein, we present the potential of a donor-acceptor (D-A) covalent conjugate of polythiophene (PTh) and perylene diimide (PDI) as an all-organic photocatalyst for the artificial photosynthesis of HO.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2023
Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, P. R. China.
The invention of near-infrared pedant-based double-cable conjugated polymers has demonstrated remarkable efficacy in single-component organic solar cells (SCOSCs). This work focuses on the innovative double-cable conjugated polymers aimed at attaining good absorption and suitable energy levels. Specifically, in the aromatic side units, the electron-donating (D) part is designed using a thieno[3,4-]pyrrole-4,6-dione (TPD) as a core unit, flanked by two cyclopentadithiophene groups on either side.
View Article and Find Full Text PDFAdv Mater
May 2023
Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Double-cable conjugated polymers with pendent electron acceptors, including fullerene, rylene diimides, and nonfused acceptors, have been developed for application in single-component organic solar cells (SCOSCs) with efficiencies approaching 10%. In this work, Y-series electron acceptors have been firstly incorporated into double-cable polymers in order to further improve the efficiencies of SCOSCs. A highly crystalline Y-series acceptor based on quinoxaline core and the random copolymerized strategy are used to optimize the ambipolar charge transport and the nanophase separation of the double-cable polymers.
View Article and Find Full Text PDFAdv Sci (Weinh)
March 2023
School of Physics, State Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, P. R. China.
Despite the simplified fabrication process and desirable microstructural stability, the limited charge transport properties of block copolymers and double-cable conjugated polymers hinder the overall performance of single-component photovoltaic devices. Based on the key distinction in the donor (D)-acceptor (A) bonding patterns between single-component and bulk heterojunction (BHJ) devices, rationalizing the difference between the transport mechanisms is crucial to understanding the structure-property correlation. Herein, the barrier formed between the D-A covalent bond that hinders electron transport in a series of single-component photovoltaic devices is investigated.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2022
Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, China.
Double-cable conjugated polymers with near-infrared (NIR) electron acceptors are synthesized for use in single-component organic solar cells (SCOSCs). Through the development of a judicious synthetic pathway, the highly sensitive nature of the 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile (IC)-based electron acceptors in basic and protonic solvents is overcome. In addition, an asymmetric design motif is adopted to optimize the packing of donor and acceptor segments, enhancing charge separation efficiency.
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