A Thieno[2,3-b]pyridine-Flanked Diketopyrrolopyrrole Polymer as an n-Type Polymer Semiconductor for All-Polymer Solar Cells and Organic Field-Effect Transistors
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pTPDPP-TF Macromolecules Manuscript ID ma-2017-00934f (for publication).pdf
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ArticleAuthors
Chen, Hung-Yang
Nikolka, Mark

Wadsworth, Andrew

Yue, Wan

Onwubiko, Ada
Xiao, Mingfei
White, Andrew J. P.
Baran, Derya

Sirringhaus, Henning
McCulloch, Iain

KAUST Department
Chemical Science ProgramKAUST Solar Center (KSC)
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
Date
2017-12-28Online Publication Date
2017-12-28Print Publication Date
2018-01-09Permanent link to this record
http://hdl.handle.net/10754/626822
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Show full item recordAbstract
A novel fused heterocycle-flanked diketopyrrolopyrrole (DPP) monomer, thieno[2,3-b]pyridine diketopyrrolopyrrole (TPDPP), was designed and synthesized. When copolymerized with 3,4-difluorothiophene using Stille coupling polymerization, the new polymer pTPDPP-TF possesses a highly planar conjugated polymer backbone due to the fused thieno[2,3-b]pyridine flanking unit that effectively alleviates the steric hindrance with both the central DPP core and the 3,4-difluorothiophene repeat unit. This new polymer exhibits a high electron affinity (EA) of −4.1 eV and was successfully utilized as an n-type polymer semiconductor for applications in organic field-effect transistors (OFETs) and all polymer solar cells. A promising n-type charge carrier mobility of 0.1 cm2 V–1 s–1 was obtained in bottom-contact, top-gate OFETs, and a power conversion efficiency (PCE) of 2.72% with a high open-circuit voltage (VOC) of 1.04 V was achieved for all polymer solar cells using PTB7-Th as the polymer donor.Citation
Chen H-Y, Nikolka M, Wadsworth A, Yue W, Onwubiko A, et al. (2017) A Thieno[2,3-b]pyridine-Flanked Diketopyrrolopyrrole Polymer as an n-Type Polymer Semiconductor for All-Polymer Solar Cells and Organic Field-Effect Transistors. Macromolecules 51: 71–79. Available: http://dx.doi.org/10.1021/acs.macromol.7b00934.Sponsors
The authors thank KAUST for financial support and acknowledge EC FP7 Project SC2 (610115) EC H2020 (643791), and EPSRC Projects EP/G037515/1 and EP/M005143/1. Mingfei Xiao thanks the Cambridge Overseas Trust and Chinese Scholarship Council for PhD funding.Publisher
American Chemical Society (ACS)Journal
MacromoleculesAdditional Links
http://pubs.acs.org/doi/10.1021/acs.macromol.7b00934Relations
Is Supplemented By:- [Dataset]
Chen, H.-Y., Nikolka, M., Wadsworth, A., Yue, W., Onwubiko, A., Xiao, M., White, A. J. P., Baran, D., Sirringhaus, H., & McCulloch, I. (2018). CCDC 1540600: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/CCDC.CSD.CC1NQ3S8. DOI: 10.5517/ccdc.csd.cc1nq3s8 Handle: 10754/663979
ae974a485f413a2113503eed53cd6c53
10.1021/acs.macromol.7b00934