On the Importance of Chemical Precision in Organic Electronics: Fullerene Intercalation in Perfectly Alternating Conjugated Polymers

The true structure of alternating conjugated polymers—the state‐of‐the‐art materials for many organic electronics—often deviates from the idealized picture. Homocoupling defects are in fact inherent to the widely used cross‐coupling polymerization methods. Nevertheless, many polymers still perform e...

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Veröffentlicht in:Advanced functional materials 2023-12, Vol.33 (52), p.n/a
Hauptverfasser: Vanderspikken, Jochen, Liu, Zhen, Wu, Xiaocui, Beckers, Omar, Moro, Stefania, Quill, Tyler James, Liu, Quan, Goossens, Arwin, Marks, Adam, Weaver, Karrie, Hamid, Mouna, Goderis, Bart, Nies, Erik, Lemaur, Vincent, Beljonne, David, Salleo, Alberto, Lutsen, Laurence, Vandewal, Koen, Van Mele, Bruno, Costantini, Giovanni, Van den Brande, Niko, Maes, Wouter
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Sprache:eng
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Zusammenfassung:The true structure of alternating conjugated polymers—the state‐of‐the‐art materials for many organic electronics—often deviates from the idealized picture. Homocoupling defects are in fact inherent to the widely used cross‐coupling polymerization methods. Nevertheless, many polymers still perform excellently in the envisaged applications, which raises the question if one should really care about these imperfections. This article looks at the relevance of chemical precision (and lack thereof) in conjugated polymers covering the entire spectrum from the molecular scale, to the micro and mesostructure, up to the device level. The different types of polymerization errors for the alkoxylated variant of the benchmark (semi)crystalline polymer poly[2,5‐bis(3‐tetradecylthiophen‐2‐yl)thieno[3,2‐b]thiophene (PBTTT) are identified, visualized, and quantified and a general strategy to avoid homocoupling is introduced. Through a combination of experiments and supported by simulations, it is shown that these coupling defects hinder fullerene intercalation and limit device performance as compared to the homocoupling‐free analog. This clearly demonstrates that structural defects do matter and should be generally avoided, in particular when the geometrical regularity of the polymer is essential. These insights likely go beyond the specific PBTTT derivatives studied here and are of general relevance for the wider organic electronics field. The relevance of careful molecular engineering of alternating conjugated polymers—for the solid‐state microstructure up to bulk (blend) material and device properties—is demonstrated here. Homocoupling defects are quantified by scanning tunneling microscopy, while rapid‐heat cool calorimetry and temperature‐resolved X‐ray diffraction analyses are combined to elucidate their effect on polymer/blend crystallinity, showing that structural defects do matter for organic electronics.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202309403