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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 218–219
DOI: https://doi.org/10.1016/j.mencom.2019.03.035
(Mi mendc1477)
 

This article is cited in 25 scientific papers (total in 25 papers)

Communications

Hole mobility in thieno[3,2-b]thiophene oligomers

V. V. Malova, T. Ghoshbc, V. C. Nairbc, M. M. Maslovd, K. P. Katind, K. N. Unnibc, A. R. Tameeva

a A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Academy of Scientific and Innovative Research (AcSIR), Thiruvananthapuram, India
c Photosciences and Photonics Section, CSIR-National Institute for Interdisciplinary Science and Technology (NIIST), Thiruvananthapuram, India
d National Research Nuclear University MEPhI, Moscow, Russian Federation
Abstract: A study of transient and steady state electrical currents in the solution-processed thin films of thieno[3,2-b]thiophene oligomers has demonstrated charge carrier mobility of about 10−2cm2V−1s−1. Thieno[3,2-b]thiophene moieties serve as reasonable charge transport sites providing the high mobility. Varying end alkyl chains in such oligomers is suggested as a viable tool to tune the mobility.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (407.9 Kb)


Citation: V. V. Malov, T. Ghosh, V. C. Nair, M. M. Maslov, K. P. Katin, K. N. Unni, A. R. Tameev, “Hole mobility in thieno[3,2-b]thiophene oligomers”, Mendeleev Commun., 29:2 (2019), 218–219
Linking options:
  • https://www.mathnet.ru/eng/mendc1477
  • https://www.mathnet.ru/eng/mendc/v29/i2/p218
  • This publication is cited in the following 25 articles:
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    2. Roman A. Irgashev, Nikita A. Kazin, “Synthesis of Thieno[3,2-b]thiophenes from 2,5-Dicarbonyl 3-Nitrothiophenes via Nucleophilic Aromatic Substitution of the Nitro Group with Thiolates”, Organics, 5:4 (2024), 507  crossref
    3. Dmitriy A. Lypenko, Alexey E. Aleksandrov, Artem V. Dmitriev, Anton A. Yakimanskiy, Ilya E. Kolesnikov, Tatiana G. Chulkova, Alexander V. Yakimansky, Alexey R. Tameev, “Photocurrent in the Polyfluorene Copolymer/PTCDI Heterojunction Enhanced by Reabsorption of Fluorescence Emission”, Chin J Polym Sci, 42:12 (2024), 1941  crossref
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    9. A.V. Khoroshutin, D.A. Lypenko, A.A. Korlyukov, A.E. Aleksandrov, P.A. Buikin, A.A. Moiseeva, A. Botezatu, S.D. Tokarev, A.R. Tameev, O.A. Fedorova, “Methoxy-substituted naphthothiophenes – Single molecules' vs. condensed phase properties and prospects for organic electronics applications”, Synthetic Metals, 287 (2022), 117094  crossref
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    12. A. S. Steparuk, S. G. Tolshchina, N. A. Kazin, R. A. Irgashev, E. F. Zhilina, A. E. Aleksandrov, A. R. Tameev, G. L. Rusinov, “New push-pull systems based on indolo[3,2-b]carbazole and 1,2,4,5-tetrazine: synthesis, photophysical, and charge transport properties”, Russ Chem Bull, 70:6 (2021), 1109  crossref
    13. Makarii I. Kozlov, Andrey N. Aslandukov, Andrey A. Vashchenko, Aleksei V. Medved'ko, Alexey E. Aleksandrov, Egor V. Latipov, Alexander S. Goloveshkin, Dmitri A. Lypenko, Alexey R. Tameev, Valentina V. Utochnikova, “Towards efficient terbium-based solution-processed OLEDs: Hole mobility increase by the ligand design”, Journal of Alloys and Compounds, 887 (2021), 161319  crossref
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    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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