Diazaisoindigo bithiophene and terthiophene copolymers for application in field‐effect transistors and solar cells
Author(s) -
Yue Wan,
Li Cheng,
Tian Xuelin,
Li Weiwei,
Neophytou Marios,
Chen Hu,
Du Weiyuan,
Jellett Cameron,
Chen HungYang,
Onwubiko Ada,
McCulloch Iain
Publication year - 2017
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.28676
Subject(s) - terthiophene , materials science , ambipolar diffusion , acceptor , polymer , copolymer , conjugated system , electron mobility , polymer chemistry , polymer solar cell , polymerization , homo/lumo , solar cell , photochemistry , chemistry , optoelectronics , electron , organic chemistry , physics , molecule , composite material , quantum mechanics , condensed matter physics
Two donor–acceptor conjugated polymers with azaisoindigo as acceptor units and bithiophene and terthiophene as donor units have been synthesized by Stille polymerization. These two polymers have been successfully applied in field‐effect transistors and polymer solar cells. By changing the donor component of the conjugated polymer backbone from bithiophene to terthiophene, the density of thiophene in the backbone is increased, manifesting as a decrease in both ionization potential and in electron affinity. Therefore, the charge transport in field‐effect transistors switches from ambipolar to predominantly hole transport behavior. PAIIDTT exhibits hole mobility up to 0.40 cm 2 /Vs and electron mobility of 0.02 cm 2 /Vs, whereas PAIIDTTT exhibits hole mobility of 0.62 cm 2 /Vs. Polymer solar cells were fabricated based on these two polymers as donors with PC 61 BM and PC 71 BM as acceptor where PAIIDTT shows a modest efficiency of 2.57% with a very low energy loss of 0.55 eV, while PAIIDTTT shows a higher efficiency of 6.16% with a higher energy loss of 0.74 eV. Our results suggest that azaisoindgo is a useful building block for the development of efficient polymer solar cells with further improvement possibility by tuning the alternative units on the polymer backbone. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2691–2699
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