Journal article
Acene ring size optimization in fused lactam polymers enabling high n-type organic thermoelectric performance
- Abstract:
- Three n-type fused lactam semiconducting polymers were synthesized for thermoelectric and transistor applications via a cheap, highly atom-efficient, and nontoxic transition-metal free aldol polycondensation. Energy level analysis of the three polymers demonstrated that reducing the central acene core size from two anthracenes (<b>A-A</b>), to mixed naphthalene-anthracene (<b>A-N</b>), and two naphthalene cores (<b>N-N</b>) resulted in progressively larger electron affinities, thereby suggesting an increasingly more favorable and efficient solution doping process when employing 4-(2,3-dihydro-1,3-dimethyl-1<i>H</i>-benzimidazol-2-yl)-<i>N</i>,<i>N</i>-dimethylbenzenamine (N-DMBI) as the dopant. Meanwhile, organic field effect transistor (OFET) mobility data showed the <b>N-N</b> and <b>A-N</b> polymers to feature the highest charge carrier mobilities, further highlighting the benefits of aryl core contraction to the electronic performance of the materials. Ultimately, the combination of these two factors resulted in <b>N-N</b>, <b>A-N</b>, and <b>A-A</b> to display power factors (PFs) of 3.2 μW m<sup>-1</sup> K<sup>-2</sup>, 1.6 μW m<sup>-1</sup> K<sup>-2</sup>, and 0.3 μW m<sup>-1</sup> K<sup>-2</sup>, respectively, when doped with N-DMBI, whereby the PFs recorded for <b>N-N</b> and <b>A-N</b> are among the highest reported in the literature for n-type polymers. Importantly, the results reported in this study highlight that modulating the size of the central acene ring is a highly effective molecular design strategy to optimize the thermoelectric performance of conjugated polymers, thus also providing new insights into the molecular design guidelines for the next generation of high-performance n-type materials for thermoelectric applications.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, 732.3KB, Terms of use)
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- Publisher copy:
- 10.1021/jacs.0c10365
Authors
- Publisher:
- American Chemical Society
- Journal:
- Journal of the American Chemical Society More from this journal
- Volume:
- 143
- Issue:
- 1
- Pages:
- 260-268
- Place of publication:
- United States
- Publication date:
- 2020-12-22
- Acceptance date:
- 2020-12-22
- DOI:
- EISSN:
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1520-5126
- ISSN:
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0002-7863
- Pmid:
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33350307
- Language:
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English
- Keywords:
- Pubs id:
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1151220
- Local pid:
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pubs:1151220
- Deposit date:
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2021-12-16
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2021
- Rights statement:
- © 2020 American Chemical Society
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from American Chemical Society at: https://doi.org/10.1021/jacs.0c10365
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