| Literature DB >> 35549036 |
Camila Cendra1, Luke Balhorn1, Weimin Zhang2, Kathryn O'Hara3, Karsten Bruening4, Christopher J Tassone4, Hans-Georg Steinrück4,5, Mengning Liang4, Michael F Toney4,6, Iain McCulloch2,7, Michael L Chabinyc3, Alberto Salleo1, Christopher J Takacs4.
Abstract
A new class of donor-acceptor (D-A) copolymers found to produce high charge carrier mobilities competitive with amorphous silicon (>1 cm2 V-1 s-1) exhibit the puzzling microstructure of substantial local order, however lacking long-range order and crystallinity previously deemed necessary for achieving high mobility. Here, we demonstrate the application of low-dose transmission electron microscopy to image and quantify the nanoscale and mesoscale organization of an archetypal D-A copolymer across areas comparable to electronic devices (≈9 μm2). The local structure is spatially resolved by mapping the backbone (001) spacing reflection, revealing nanocrystallites of aligned polymer chains throughout nearly the entire film. Analysis of the nanoscale structure of its ordered domains suggests significant short- and medium-range order and preferential grain boundary orientations. Moreover, we provide insights into the rich, interconnected mesoscale organization of this new family of D-A copolymers by analysis of the local orientational spatial autocorrelations.Entities:
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Year: 2021 PMID: 35549036 DOI: 10.1021/acsmacrolett.1c00547
Source DB: PubMed Journal: ACS Macro Lett ISSN: 2161-1653 Impact factor: 6.903