2019
DOI: 10.1002/aenm.201900044
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Achieving Thickness‐Insensitive Morphology of the Photoactive Layer for Printable Organic Photovoltaic Cells via Side Chain Engineering in Nonfullerene Acceptors

Abstract: Although high power conversion efficiency of over 14% has been achieved using nonfullerene acceptors (NFAs) in organic photovoltaics (OPVs), securing their insensitive device performance to the thickness of the photoactive layer remains an indispensable requirement for their successful commercialization via printing technologies. In this study, by synthesizing a new series of ITIC‐based NFAs having alkyl or alkoxy groups, it is found that the bulk heterojunction morphology dependence on the thickness of the ph… Show more

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Cited by 39 publications
(24 citation statements)
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References 54 publications
(95 reference statements)
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“…Here, we synthesized an alkoxy‐substituted A–D–A FREA F10IC2 (chemical structure is shown in Figure a), where the decacyclic core benefited intermolecular interaction and charge transporting between molecules. The alkoxy side chains of F10IC2 not only extended the absorption of FREA due to the inductive effect of oxygen atoms, but also could greatly increase the solubility of F10IC2 relative to the alkyl‐substituted analogue, enabling the process in nonchlorinated solvents. F10IC2 showed complementary absorption and matched energy levels with the commercial polymer donor PTB7‐Th (Figure a).…”
Section: Introductionmentioning
confidence: 99%
“…Here, we synthesized an alkoxy‐substituted A–D–A FREA F10IC2 (chemical structure is shown in Figure a), where the decacyclic core benefited intermolecular interaction and charge transporting between molecules. The alkoxy side chains of F10IC2 not only extended the absorption of FREA due to the inductive effect of oxygen atoms, but also could greatly increase the solubility of F10IC2 relative to the alkyl‐substituted analogue, enabling the process in nonchlorinated solvents. F10IC2 showed complementary absorption and matched energy levels with the commercial polymer donor PTB7‐Th (Figure a).…”
Section: Introductionmentioning
confidence: 99%
“…76−79 The benzodithiophenedione unit, which has high planarity and conductivity, has been widely studied in recent years, which has high crystallinity and hole mobility, and hence performs very well in a variety of NFA systems and thick-film devices. [80][81][82] Its fluorinated derivative PM6 and chlorinated derivative PM7 also show excellent performance with various NFAs such as the IDIC, 31,[83][84][85] ITIC, 31,86,87 and Y6 derivatives. 1,88-90 A wide range of polymer donors with high planarity and charge mobility have also been included in thick-film devices.…”
Section: 14mentioning
confidence: 99%
“…Copolymers based on fluorinated benzotriazole (FBTA) derivatives have been well studied in thick junctions 76 . − 79 The benzodithiophenedione unit, which has high planarity and conductivity, has been widely studied in recent years, which has high crystallinity and hole mobility, and hence performs very well in a variety of NFA systems and thick‐film devices 80–82 . Its fluorinated derivative PM6 and chlorinated derivative PM7 also show excellent performance with various NFAs such as the IDIC, 31,83–85 ITIC, 31,86,87 and Y6 derivatives 1,88–90 .…”
Section: Molecular Design Strategies For Thickness‐insensitive Materialsmentioning
confidence: 99%
“…The charge recombination will become serious along with the increase in active layer thickness, which is mainly due to the low charge mobility of organic photoactive materials and unfavorable morphology in thick active layers. [ 35–38 ] The severe charge recombination in thick active layers will drastically decrease the FF and PCE of thick‐film OSCs. [ 39,40 ] An urgent scheme is needed to find ways to reduce charge recombination in thick active layers for achieving highly efficient thick‐film OSCs.…”
Section: Introductionmentioning
confidence: 99%