Synthesis and characterization of low bandgap π-conjugated copolymers incorporating 4,7-bis(3,3′/4,4′-hexylthiophene-2-yl)benzo[c][2,1,3]thiadiazole units for photovoltaic application

被引:34
作者
Abdo, Nabiha I. [1 ,2 ,3 ]
Ku, Jamin [1 ,2 ]
El-Shehawy, Ashraf A. [1 ,2 ,4 ]
Shim, Hee-Sang [3 ]
Min, Joon-Keun [1 ,2 ,3 ]
El-Barbary, Ahmed A.
Jang, Yun Hee [1 ,2 ]
Lee, Jae-Suk [1 ,2 ,3 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Mat Sci & Engn, Kwangju 500712, South Korea
[2] Gwangju Inst Sci & Technol, Dept Nanobio Mat & Elect, Kwangju 500712, South Korea
[3] Gwangju Inst Sci & Technol, Res Inst Solar & Sustainable Energies, Kwangju 500712, South Korea
[4] Kafr El Sheikh Univ, Dept Chem, Fac Sci, Kafr Al Sheikh 33516, Egypt
基金
新加坡国家研究基金会;
关键词
POLYMER SOLAR-CELLS; C-H ARYLATION; PHOTOINDUCED ELECTRON-TRANSFER; OPEN-CIRCUIT VOLTAGE; POLYFLUORENE COPOLYMER; ELECTROCHEMICAL PROPERTIES; OPTOELECTRONIC PROPERTIES; SEMICONDUCTING POLYMERS; RATIONAL DESIGN; PERFORMANCE;
D O I
10.1039/c3ta11433c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
4,7-Bis(3,3'/4,4'-hexylthiophene-2-yl)benzo[c][2,1,3]thiadiazoles (HT-BT-HT) were used as building blocks to construct a series of low bandgap pi-conjugated copolymers for photovoltaic applications. The desired copolymers were obtained by incorporating the HT-BT-HT comonomers together with donor or acceptor units, such as 3,4-ethylenedioxythiophene (EDOT), bis-EDOT, thieno[3,4-b]pyrazine (TP), and 2,3-dimethyl-TP, via a palladium-catalyzed Stille cross-coupling method. A facile synthetic method has also been developed for the synthesis of several EDOT- and TP-based copolymers via direct C-H arylation of EDOT, bis-EDOT, and TP derivatives using the commercially available catalyst Pd(OAc)(2) under Heck-type experimental conditions (Jeffery method). For all of the synthesized copolymers, moving the hexyl side chains of the HT unit in the HT-BT-HT comonomers from 3,3'-positions (close to BT, as in P1-P4) to 4,4'-positions (away from BT, as in P5-P8) led to a significant red shift of the UV-vis absorption spectrum, a decrease of the energy bandgap, an increase of the glass transition temperature, and more promising photovoltaic performances. The thin-film copolymer P7 incorporating TP units (-TP-HT-BT-HT-)(n) exhibited the most extended absorption (beyond 1000 nm) and the lowest optical bandgap (1.24 eV) among the synthesized copolymers. According to time-dependent density functional theory calculations, the TP unit, in contrast to EDOT, has its lowest unoccupied molecular orbital (LUMO) at the same level as BT. An extended pi-conjugation along the TP and BT units leads to low-lying LUMO levels of the resulting copolymer P7 and in turn its reduced bandgap. The power conversion efficiencies (PCEs) of organic photovoltaic devices employing copolymers P1-P8 were measured in the configuration of ITO/PEDOT:PSS/copolymer (P1-P8) : PC60BM (1 : 1 w/w)/Al. Copolymer P7 in particular showed the highest PCE of 3.32%.
引用
收藏
页码:10306 / 10317
页数:12
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