2023
DOI: 10.1016/j.cej.2022.139489
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Solid-liquid convertible fluorinated terthiophene as additives in mediating morphology and performance of organic solar cells

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Cited by 18 publications
(16 citation statements)
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“…When the solution concentration increased, PBDT-TTz chains with a more extended and rigid chain conformation reduced entanglements between molecular chains and enhanced interchain π–π stacking. In addition, increasing the concentration would further promote the intrachain self-folding, thus forming a more compact ordered aggregation, which would be conducive to the carrier transport within and between molecular chains …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…When the solution concentration increased, PBDT-TTz chains with a more extended and rigid chain conformation reduced entanglements between molecular chains and enhanced interchain π–π stacking. In addition, increasing the concentration would further promote the intrachain self-folding, thus forming a more compact ordered aggregation, which would be conducive to the carrier transport within and between molecular chains …”
Section: Resultsmentioning
confidence: 99%
“…In addition, increasing the concentration would further promote the intrachain self-folding, 66 thus forming a more compact ordered aggregation, which would be conducive to the carrier transport within and between molecular chains. 67 As an external field, solvent plays an identical role to force, temperature, and electricity in the solution state, and it has a weak stimulating effect with a strong response from conjugated polymer chains. 68,69 With the removal of solvent, the distances between chains become shortened and the degree of macroscopic aggregation increases.…”
Section: Hole Mobility Characteristics and Solar Cell Examinationmentioning
confidence: 99%
“…The first type of solid additive, such as benzothiadiazole (BT), dihalogenated 1,1-dicyanomethylene-3-indanone (IC-FI), and 2,2′:5′,2′′-terthiophene ([2H]3T), features a characteristic chemical molecular group with active layer components to ensure compatibility with the donor or acceptor. [21][22][23] The second type of solid additive contains halogen atoms with specific charge distributions that induce intermolecular interaction between the solid additive and active layer components via halogen bonding (e.g., 1,4-diiodotetrafluorobenzene (A3), 1,3-dibromo-5chlorobenzene (DBCl), and 1,4-diiodobenzene (DIB)). [24][25][26] The last type of solid additive is highly crystalline molecules such as dithieno[3,2-b:2′,3′-d]thiophene (DTT), anthracene (An), naphthalene (NA), and 2,7-dibromo-9,9-dimethylfluorene (DBDMF) that inhibit overaggregation in acceptor molecules.…”
Section: Introductionmentioning
confidence: 99%
“…in view of chemical structures (Figure S1). As regards to the conjugated skeletons, the simple thiophene unit would be the most likely choice as it (1) exists in all high performance OSC molecules, (2) could interact with those OSC molecules through both strong π–π stackings and widely observed sulfur-halogen secondary interactions, , and (3) would further increase the capacity for better crystallization due to easy addition of halogen atoms on such a thiophene ring, which may act as a crystal seed to optimize morphologies of active layers. In short, these combined features of simple halogenated thiophene thus would make it a promising solid additive, despite that such an analysis was rarely reported …”
mentioning
confidence: 99%