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Dopant-dependent thermoelectric performance of indoloindole-selenophene based conjugated polymer
  • Min Han, Ji ;
  • Eun Yoon, Sang ;
  • Hyun Jung, Ku ;
  • Bae, Onyu ;
  • Kim, Donguk ;
  • Kim, Unjeong ;
  • Seo, Hyungtak ;
  • Sunjoo Kim, Felix ;
  • Chul Kim, Ki ;
  • Kim, Jong H. ;
  • Kim, Bong Gi
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Publication Year
2022-03-01
Publisher
Elsevier B.V.
Citation
Chemical Engineering Journal, Vol.431
Keyword
Conjugated polymerDoping mechanismMolecular dopantOrganic conductorOrganic thermoelectrics
Mesh Keyword
Doping mechanismElectron-donatingHigh electrical conductivityMolecular dopantOrganic thermoelectricOrganicsSelenopheneSynthesisedThermoelectricThermoelectric performance
All Science Classification Codes (ASJC)
Chemistry (all)Environmental ChemistryChemical Engineering (all)Industrial and Manufacturing Engineering
Abstract
The development of organic conductors, which exhibit high electrical conductivity through chemical doping using non-acidic molecular dopants, has been challenging because of inefficient generation of free charge carriers. In this study, we synthesized a new conjugated polymer (CP) containing electron-donating indoloindole and biselenophene to devise an efficient doping platform. When the synthesized CPs were doped with electron acceptor (F4TCNQ) and Lewis acid (AuCl3) type dopants, both dopants realized high electrical conductivities (184 S·cm−1 for F4TCNQ and 283 S·cm−1 for AuCl3). Furthermore, the binding energies of the electron-donating atoms in the doped CPs and the degree of stabilization energy before/after doping indicated that Se and N atoms tended to interact more favorably with F4TCNQ and AuCl3, respectively. However, the Seebeck coefficient and power factor of the AuCl3-doped CP were lower than those of the F4TCNQ-doped CP, which was attributed to the larger amount of charge carriers generated by the AuCl3 dopant.
ISSN
1385-8947
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32426
DOI
https://doi.org/10.1016/j.cej.2021.133779
Fulltext

Type
Article
Funding
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT ( NRF-2021R1A2C4002030 and NRF-2021R1A2C1007304 ). This work was also supported by Korea Institute for Advancement of Technology(KIAT) grant funded by the Korea Government ( MOTIE , P0012770 ).
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SEO, HYUNGTAK서형탁
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