2021
DOI: 10.1016/j.joule.2020.11.006
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Efficient Organic Solar Cells from Molecular Orientation Control of M-Series Acceptors

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Cited by 209 publications
(174 citation statements)
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“…On the one hand, the conjugated backbones in these building blocks should be planar and rigid, which is beneficial for π-electron delocalization and intramolecular charge transport. As these fused-ring building blocks, all contain a few sulfur-and/or nitrogen-heteroaromatic five-membered rings and thus are electron-rich 4 , 8 , 17 , a strong intramolecular charge transfer (ICT) effect can be formed when they conjugately link with the electron-deficient end-capping groups, which endows the flexibilities in modulating absorption spectra and molecular energy levels of the NFAs 24 27 . On the other hand, the bulky alkyls on the fused-ring building blocks not only guarantee good solubilities of the NFAs 25 , 27 , 28 but also ensure the intermolecular π−π stacking of the NFAs to mainly occur at the end-capping groups, because such a molecular packing mode is crucial for their electron-accepting capability 19 , 20 , 29 31 .…”
Section: Introductionmentioning
confidence: 99%
“…On the one hand, the conjugated backbones in these building blocks should be planar and rigid, which is beneficial for π-electron delocalization and intramolecular charge transport. As these fused-ring building blocks, all contain a few sulfur-and/or nitrogen-heteroaromatic five-membered rings and thus are electron-rich 4 , 8 , 17 , a strong intramolecular charge transfer (ICT) effect can be formed when they conjugately link with the electron-deficient end-capping groups, which endows the flexibilities in modulating absorption spectra and molecular energy levels of the NFAs 24 27 . On the other hand, the bulky alkyls on the fused-ring building blocks not only guarantee good solubilities of the NFAs 25 , 27 , 28 but also ensure the intermolecular π−π stacking of the NFAs to mainly occur at the end-capping groups, because such a molecular packing mode is crucial for their electron-accepting capability 19 , 20 , 29 31 .…”
Section: Introductionmentioning
confidence: 99%
“…The strong (100) peak locates at q xy ≈ 0.28 Å −1 in the in‐plane (IP) direction (lamellar stacking) and the significant (010) peak at q z ≈ 1.76 Å −1 in the out‐of‐plane (OOP) direction (π–π stacking) indicate that the (w/o) blend film manifests a distinct face‐on orientation. [ 32 ] When the solvent additive CN is added into PM6:Y6, the intensities in both the IP direction and the OOP direction have been enhanced. The identical position of the diffraction peaks indicates the film remain pristine molecular orientation, whereas the enhanced intensity exhibits the film with a stronger crystallinity.…”
Section: Resultsmentioning
confidence: 99%
“…Generally, the optoelectronic properties and packing structures of NFAs can be regulated by changing the central D and terminal A units [15,16] . As a result, NFAs have rapidly led the development of OSCs in recent years [17] and the PCEs of OSCs based on A-D-A-type NFAs have surpassed 16% [18,19] . More encouragingly, Y6, a superior NFA with 2,1,3-benzothiadiazole (BT) as the central electron-deficient core in the A-DA'D-A structure was proposed by Yuan et al [20] in 2019, which demonstrated a remarkable PCE of 15.7% in its first report.…”
Section: Introductionmentioning
confidence: 99%