Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/81623
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dc.contributorDepartment of Electronic and Information Engineeringen_US
dc.creatorTang, Hen_US
dc.creatorXu, Ten_US
dc.creatorYan, Cen_US
dc.creatorGao, Jen_US
dc.creatorYin, Hen_US
dc.creatorLv, Jen_US
dc.creatorSingh, Ren_US
dc.creatorKumar, Men_US
dc.creatorDuan, Ten_US
dc.creatorKan, Zen_US
dc.creatorLu, Sen_US
dc.creatorLi, Gen_US
dc.date.accessioned2020-01-21T08:49:14Z-
dc.date.available2020-01-21T08:49:14Z-
dc.identifier.issn2198-3844en_US
dc.identifier.urihttp://hdl.handle.net/10397/81623-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Tang, H., Xu, T., Yan, C., Gao, J., Yin, H., Lv, J., ... & Lu, S. (2019). Donor Derivative Incorporation: An Effective Strategy toward High Performance All‐Small‐Molecule Ternary Organic Solar Cells. Advanced Science, 6(21), 1901613, 1-8 is available at https://doi.org/10.1002/advs.201901613en_US
dc.subjectMorphologyen_US
dc.subjectOrganic solar cellsen_US
dc.subjectSmall moleculesen_US
dc.subjectStructural similarityen_US
dc.subjectThick filmsen_US
dc.titleDonor Derivative Incorporation : an effective strategy toward high performance all-small-molecule ternary organic solar cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1002/advs.201901613en_US
dcterms.abstractThick-film all-small-molecule (ASM) organic solar cells (OSCs) are preferred for large-scale fabrication with printing techniques due to the distinct advantages of monodispersion, easy purification, and negligible batch-to-batch variation. However, ASM OSCs are typically constrained by the morphology aspect to achieve high efficiency and maintain thick film simultaneously. Specifically, synchronously manipulating crystallinity, domain size, and phase segregation to a suitable level are extremely challenging. Herein, a derivative of benzodithiophene terthiophene rhodanine (BTR) (a successful small molecule donor for thick-film OSCs), namely, BTR-OH, is synthesized with similar chemical structure and absorption but less crystallinity relative to BTR, and is employed as a third component to construct BTR:BTR-OH:PC71BM ternary devices. The power conversion efficiency (PCE) of 10.14% and fill factor (FF) of 74.2% are successfully obtained in ≈300 nm OSC, which outperforms BTR:PC71BM (9.05% and 69.6%) and BTR-OH:PC71BM (8.00% and 65.3%) counterparts, and stands among the top values for thick-film ASM OSCs. The performance enhancement results from the enhanced absorption, suppressed bimolecular/trap–assisted recombination, improved charge extraction, optimized domain size, and suitable crystallinity. These findings demonstrate that the donor derivative featuring similar chemical structure but different crystallinity provides a promising third component guideline for high-performance ternary ASM OSCs.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 6 Nov. 2019, 1901613, 1-8en_US
dcterms.isPartOfOccupational therapy internationalen_US
dcterms.issued2019-11-06-
dc.identifier.scopus2-s2.0-85071742835-
dc.identifier.artn1901613en_US
dc.description.validate202001 bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0669-n37, OA_Scopus/WOSen_US
dc.description.pubStatusPublisheden_US
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