Please use this identifier to cite or link to this item:
https://hdl.handle.net/20.500.14279/14067
Title: | The Role of the Side Chain on the Performance of N-type Conjugated Polymers in Aqueous Electrolytes | Authors: | Giovannitti, Alexander Maria, Iuliana Petruta Hanifi, David Donahue, Mary J Bryant, Daniel Barth, Katrina J Makdah, Beatrice E Savva, Achilleas Moia, Davide Zetek, Matyáš Barnes, Piers R F Reid, Obadiah G Inal, Sahika Rumbles, Garry Malliaras, George G Nelson, Jenny Rivnay, Jonathan McCulloch, Iain |
Major Field of Science: | Engineering and Technology | Field Category: | Mechanical Engineering | Keywords: | Transistors;Thin film transistors;Electrochemical transistor | Issue Date: | 8-May-2018 | Source: | Chemistry of Materials, 2018, vol. 30, no. 9, pp. 2945-2953 | Volume: | 30 | Issue: | 9 | Start page: | 2945 | End page: | 2953 | Journal: | Chemistry of Materials | Abstract: | We report a design strategy that allows the preparation of solution processable n-type materials from low boiling point solvents for organic electrochemical transistors (OECTs). The polymer backbone is based on NDI-T2 copolymers where a branched alkyl side chain is gradually exchanged for a linear ethylene glycol-based side chain. A series of random copolymers was prepared with glycol side chain percentages of 0, 10, 25, 50, 75, 90, and 100 with respect to the alkyl side chains. These were characterized to study the influence of the polar side chains on interaction with aqueous electrolytes, their electrochemical redox reactions, and performance in OECTs when operated in aqueous electrolytes. We observed that glycol side chain percentages of >50% are required to achieve volumetric charging, while lower glycol chain percentages show a mixed operation with high required voltages to allow for bulk charging of the organic semiconductor. A strong dependence of the electron mobility on the fraction of glycol chains was found for copolymers based on NDI-T2, with a significant drop as alkyl side chains are replaced by glycol side chains. | ISSN: | 08974756 | DOI: | 10.1021/acs.chemmater.8b00321 | Rights: | © American Chemical Society. | Type: | Article | Affiliation : | Imperial College London Stanford University École Nationale Supérieure des Mines King Abdullah University of Science and Technology Northwestern University University of Colorado National Renewable Energy Laboratory University of Cambridge Cyprus University of Technology |
Publication Type: | Peer Reviewed |
Appears in Collections: | Άρθρα/Articles |
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