Synthesis and side-chain engineering of phenylnaphthalenediimide (PNDI)-based n-type polymers for efficient all-polymer solar cells
We designed and synthesized a series of n-type conjugated polymers by introducing phenylnaphthalenediimide (PNDI) as a novel n-type building block, and investigated the effect of side-chain engineering of the polymer acceptors on the performance of all-polymer solar cells (all-PSCs). The optical, el...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 5; no. 11; pp. 5449 - 5459 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
2017
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Subjects | |
Online Access | Get full text |
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Summary: | We designed and synthesized a series of n-type conjugated polymers by introducing phenylnaphthalenediimide (PNDI) as a novel n-type building block, and investigated the effect of side-chain engineering of the polymer acceptors on the performance of all-polymer solar cells (all-PSCs). The optical, electrochemical, and structural properties of the polymers with three different side chains of 2-ethylhexyl (PPNDI-EH), 2-butyloctyl (PPNDI-BO), and 2-hexyldecyl (PPNDI-HD) groups were examined. Interestingly, the PNDI-based polymer having the longest side chain showed a higher degree of edge-on oriented intermolecular assembly in thin films, thereby resulting in the highest field-effect electron mobility among the three polymers. Also, we examined the performance of PNDI-based polymers as polymer acceptors in all-PSCs. Unlike the trend in the field-effect transistor, the PPNDI-BO-based all-PSCs exhibited the highest power conversion efficiency (PCE) of 4.25% among the three polymer blends. This was attributed to the well-balanced hole/electron transport and higher exciton dissociation probability in the PPNDI-BO-based all-PSCs, benefitted from the well-intermixed blend morphology between the polymer donor and PPNDI-BO. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c6ta10978k |