Experimental evidence that short-range intermolecular aggregation is sufficient for efficient charge transport in conjugated polymers

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 112; no. 34; pp. 10599 - 10604
• Main Authors: Wang, Suhao, Fabiano, Simone, Himmelberger, Scott, Puzinas, Skomantas, Crispin, Xavier, Salleo, Alberto, Berggren, Magnus
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 25.08.2015; National Acad Sciences
• Subjects: Crystallography; Diffraction; Matrix; Physical Sciences; Polymer films; aggregation; organic electronics; charge transport; conjugated polymers
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1501381112

Efficiency, current throughput, and speed of electronic devices are to a great extent dictated by charge carrier mobility. The classic approach to impart high carrier mobility to polymeric semiconductors has often relied on the assumption that extensive order and crystallinity are needed. Recently, however, this assumption has been challenged, because high mobility has been reported for semiconducting polymers that exhibit a surprisingly low degree of order. Here, we show that semiconducting polymers can be confined into weakly ordered fibers within an inert polymer matrix without affecting their charge transport properties. In these conditions, the semiconducting polymer chains are inhibited from attaining long-range order in the π-stacking or alkyl-stacking directions, as demonstrated from the absence of significant X-ray diffraction intensity corresponding to these crystallographic directions, yet still remain extended along the backbone direction and aggregate on a local length scale. As a result, the polymer films maintain high mobility even at very low concentrations. Our findings provide a simple picture that clarifies the role of local order and connectivity of domains.