Alkynyl-Functionalized Head-to-Head Linkage Containing Bithiophene as a Weak Donor Unit for High-Performance Polymer Semiconductors

Yulun Wang, Qiaogan Liao, Gang Wang, Han Guo, Xianhe Zhang, Mohammad Afsar Uddin, Shengbin Shi, Huimin Su, Junfeng Dai, Xing Cheng, Antonio Facchetti, Tobin J Marks, Xugang Guo

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Building blocks having a high degree of backbone planarity, good solubilizing characteristics, and well-tailored physicochemical properties are highly desirable for constructing high-performance polymer semiconductors. Due to the detrimental steric hindrance created by alkyl chain substituents at the 3- and 3′-positions of bithiophene, "head-to-head" linkage containing 3,3′-dialkyl-2,2′-bithiophenes (BTR) are typically avoided in materials design. Replacing alkyl chains with less steric demanding alkynyl chains should greatly reduce steric hindrance by eliminating two H atoms at the sp-hybridized carbon center. Here we report the synthesis of a novel electron donor unit, 3,3′-dialkynyl-2,2′-bithiophene (BTRy), and its incorporation into conjugated polymer backbones. The alkynyl-functionalized head-to-head bithiophene linkage yields polymers with good solubility without sacrificing backbone planarity; the BTRy-based polymers show a high degree of conjugation with a narrow bandgap of ∼1.6 eV. When incorporated into organic thin-film transistors, the polymers exhibit substantial hole mobility, up to 0.13 cm2 V-1 s-1 in top-gated transistors. The electron-withdrawing alkynyl substituents lower the frontier molecular orbitals, imbuing the difluorobenzothiadiazole and difluorobenzoxadiazole copolymers with remarkable ambipolarity: electron mobility > 0.05 cm2 V-1 s-1 and hole mobility ∼0.01 cm2 V-1 s-1 in bottom-gated transistors. In bulk-heterojunction solar cells, the BTRy-based polymers show promising power conversion efficiencies approaching 8% with very large Voc values of 0.91-1.04 V, due to the weak electron-withdrawing alkynyl substituents. In comparison to the tetrathiophene-based polymer analogues based on the unsubstituted π-spacer design, the BTRy-based polymers have comparable light absorption but with 0.14 V larger open-circuit voltage, translating to enhanced optoelectronic properties for this attractive design strategy. Thus, alkynyl groups are versatile semiconductor substituents, offering good solubility, substantial backbone planarity, optimized optoelectronic properties, and film crystallinity, for materials innovation in organic electronics.

Original languageEnglish
Pages (from-to)4109-4121
Number of pages13
JournalChemistry of Materials
Volume29
Issue number9
DOIs
Publication statusPublished - May 9 2017

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Polymers
Semiconductor materials
Hole mobility
Optoelectronic devices
Electrons
Transistors
Solubility
Electron mobility
Conjugated polymers
Molecular orbitals
Open circuit voltage
Thin film transistors
Light absorption
Conversion efficiency
Heterojunctions
Solar cells
Energy gap
Electronic equipment
Carbon
Copolymers

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)
  • Materials Chemistry

Cite this

Alkynyl-Functionalized Head-to-Head Linkage Containing Bithiophene as a Weak Donor Unit for High-Performance Polymer Semiconductors. / Wang, Yulun; Liao, Qiaogan; Wang, Gang; Guo, Han; Zhang, Xianhe; Uddin, Mohammad Afsar; Shi, Shengbin; Su, Huimin; Dai, Junfeng; Cheng, Xing; Facchetti, Antonio; Marks, Tobin J; Guo, Xugang.

In: Chemistry of Materials, Vol. 29, No. 9, 09.05.2017, p. 4109-4121.

Research output: Contribution to journalArticle

Wang, Y, Liao, Q, Wang, G, Guo, H, Zhang, X, Uddin, MA, Shi, S, Su, H, Dai, J, Cheng, X, Facchetti, A, Marks, TJ & Guo, X 2017, 'Alkynyl-Functionalized Head-to-Head Linkage Containing Bithiophene as a Weak Donor Unit for High-Performance Polymer Semiconductors', Chemistry of Materials, vol. 29, no. 9, pp. 4109-4121. https://doi.org/10.1021/acs.chemmater.7b01052
Wang, Yulun ; Liao, Qiaogan ; Wang, Gang ; Guo, Han ; Zhang, Xianhe ; Uddin, Mohammad Afsar ; Shi, Shengbin ; Su, Huimin ; Dai, Junfeng ; Cheng, Xing ; Facchetti, Antonio ; Marks, Tobin J ; Guo, Xugang. / Alkynyl-Functionalized Head-to-Head Linkage Containing Bithiophene as a Weak Donor Unit for High-Performance Polymer Semiconductors. In: Chemistry of Materials. 2017 ; Vol. 29, No. 9. pp. 4109-4121.
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