Conformation-Insensitive Ambipolar Charge Transport in a Diketopyrrolopyrrole-Based Co-polymer Containing Acetylene Linkages
Source abstract
Abstract
A new donor–acceptor organic semiconducting co-polymer (PDPP-TAT) containing acetylene linkages based on dithienyl-diketopyrrolopyrrole (tDPP) has been synthesized and compared with a tDPP-based co-polymer (PDPP-TVT) containing vinylene linkages. The sp -hybridized carbons in the acetylene linkages result in favorable overlap of the electron wave functions of the tDPP units along the main chain. Further, the π-conjugation of PDPP-TAT was found to be highly insensitive to the chain conformation, in contrast to that of PDPP-TVT. As a result, PDPP-TAT provides favorable charge transport for electrons as well as holes, and enables facile charge transport in amorphous and tie-molecular regions connecting its crystalline domains. PDPP-TAT exhibits ambipolar characteristics with a high electron/hole mobility ratio (μ e /μ h ) of ∼0.3 in field-effect transistors, whereas PDPP-TVT exhibits unipolar characteristics with a μ e /μ h value that is a factor of 30 lower. Our results demonstrate that the conformation sensitivity of charge transport is a vital factor in the electrical performances of actual organic transistor devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering, Research Institute for Green Energy Convergence Technology (REGET), Gyeongsang National University, Jinju 660-701, Korea
Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH) and Center for Advanced Soft Electronics (CASE), Pohang 790-784, Korea
Department of Chemistry, Gyeongsang National University and Research Institute of Nature Science (RINS), Jinju 660-701, Korea
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