An investigation of the role acceptor side chains play in the processibility and efficiency of organic solar cells fabricated from small molecular donors featuring 3,4-ethylenedioxythiophene cores.
Autor: | Mica NA; Organic Semiconductor Centre, SUPA, School of Physics and Astronomy St Andrews Fife KY16 9SS UK., Almahmoud SAJ; Glasgow Centre for Physical Organic Chemistry (GCPOC), WestCHEM, School of Chemistry, University of Glasgow Glasgow G12 8QQ UK., Krishnan Jagadamma L; Organic Semiconductor Centre, SUPA, School of Physics and Astronomy St Andrews Fife KY16 9SS UK., Cooke G; Glasgow Centre for Physical Organic Chemistry (GCPOC), WestCHEM, School of Chemistry, University of Glasgow Glasgow G12 8QQ UK., Samuel IDW; Organic Semiconductor Centre, SUPA, School of Physics and Astronomy St Andrews Fife KY16 9SS UK. |
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Jazyk: | angličtina |
Zdroj: | RSC advances [RSC Adv] 2018 Nov 23; Vol. 8 (69), pp. 39231-39240. Date of Electronic Publication: 2018 Nov 23 (Print Publication: 2018). |
DOI: | 10.1039/c8ra07034b |
Abstrakt: | Organic photovoltaic devices fabricated from small molecular donors continue to receive significant interest due to their desirable properties such as convenient synthesis, purification and batch-to-batch reproducibility. In this study, we have synthesized two small molecules based on an alternating A-D-A structure, utilizing a central EDOT donor moiety and either 2-ethylhexyl cyanoacetate (SAM-72) or N -(2-ethylhexyl)cyanoacetamide (SAM-80) units as acceptor termini. The small molecules were incorporated into bulk heterojunction solar cells with PC Competing Interests: There are no conflicts to declare. (This journal is © The Royal Society of Chemistry.) |
Databáze: | MEDLINE |
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