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Fully non-fused ring acceptor (FNFRA) are potentially important for boosting the performance and lowering the material costs of organic solar cells (OSCs). Despite their potential, FNFRA-based OSCs have not yet matched the performance of their fused ring and partial non-fused ring counterparts due to limited molecular engineering research. In this work, by incorporating a synergistic strategy of tailoring the β-side chain and end-group of FNFRA with the cyclic "belt" simultaneously, a FNFRA named C6FT-2F2Cl is constructed. Compared with other symmetric FNFRAs, C6FT-2F2Cl features a shorter π-π stacking distance and an efficient zigzag charge transport channel, leading to enhanced and balanced charge carrier mobilities, lower non-radiative energy loss and a higher short-circuit current density. The power conversion efficiency (PCE) of the C6FT-2F2Cl-based OSC reached 13.19%, which is among the best in FNFRA-based devices. This work provides new valuable insights for the charge transport mechanism associated FNFRAs and paves a new route to the materials design toward high-performance and low-cost OSCs.
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http://dx.doi.org/10.1002/marc.202401037 | DOI Listing |
Ann Thorac Surg
August 2025
Purpose: To describe technique of tricuspidization of the bicuspid aortic valve (BAV).
Description: Six patients with very asymmetrical aortic cusp and three sinuses had tricuspidization. Age was 32.
ACS Appl Mater Interfaces
August 2025
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.
Fused-ring electron acceptors (FREAs) have advanced significantly in organic solar cells (OSCs) but suffer from complex synthesis and high production costs. As a cost-effective alternative, nonfused-ring electron acceptors (NFREAs) offer structural simplicity and easier synthesis, though typically at the expense of device performance. In this work, two asymmetric NFREAs, 3TT-CF and 3TT-BCF, were synthesized via a modular strategy and applied in high-efficiency OSCs.
View Article and Find Full Text PDFNon-fullerene acceptor materials characterized by fused ring structures have garnered considerable attention due to their tunable molecular architectures, extensive and robust absorption spectra, and high photoelectric conversion efficiencies. Nonetheless, these materials present challenges, such as complex synthetic processes, elevated costs, and significant fabrication difficulties, which markedly impede their commercial viability. In light of these challenges, exploration of non-fused ring acceptors that are easier to synthesize and exhibit superior device characteristics has been proposed as a promising solution.
View Article and Find Full Text PDFNat Commun
July 2025
Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou, PR China.
Toward commercialization of organic solar cells (OSCs), photoactive materials that enable high efficiency yet possess low cost should be developed. Fully non-fused ring electron acceptors (FNEAs) that extend the conjugated skeleton with carbon-carbon (C-C) single bonds solely have lower synthetic costs than their fused-ring counterparts. However, the power conversion efficiencies (PCEs) of FNEAs are lagging due to low acceptor crystallinity and difficulty in the formation of fibrillary bi-continuous interpenetrating network morphology.
View Article and Find Full Text PDFJ Phys Chem B
March 2025
School of Materials Science and Engineering, Yancheng Institute of Technology, Yancheng 224051, P. R. China.
The development of nonfused ring electron acceptors (NFREAs) has garnered significant attention due to their simplified molecular design and cost-effectiveness. Recent advancements have pushed the power conversion efficiency (PCE) of NFREAs beyond 19%. Despite these advantages, most NFREAs adopt A-D-A structures, where the electron-donating core is typically a benzene ring substituted with fluorine or alkoxy groups.
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