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Insights into the influence of fluorination positions on polymer donor materials on photovoltaic performance
Affiliation:1. Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing 100875, China;2. State Key Laboratory for Mechanical Behavior of Materials, Xi''an Jiaotong University, Xi''an 710049, China;3. State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China;1. Key Laboratory of Special Functional Materials, South China University of Technology, Guangzhou 510640, People’s Republic of China;2. Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, People’s Republic of China;3. College of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People’s Republic of China;1. College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China;2. Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovský Sq. 2, 162 06 Prague 6, Czech Republic;3. Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China;1. Department of Chemistry Education, Institute of Fusion Science, Div. of Science Education, Chonbuk National University, 567 Baekje-ro, Jeonju 561-756, Republic of Korea;2. Professional Graduate School of Flexible and Printable Electronics, Polymer Materials Fusion Research Center, Chonbuk National University, 567 Baekje-ro, Jeonju 561-756, Republic of Korea;3. Department of Chemistry, Dongguk University-Seoul, Seoul 100-715, Republic of Korea;1. Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, Beijing Normal University, Beijing 100875, China;2. College of Chemistry and Chemical Engineering, Shanxi Datong University, Datong 037009, China
Abstract:To explore the influence of fluoro substitution position and number on optical, electrochemical and photovoltaic properties, three novel donor-acceptor (D-A) alternative copolymers (PHF, PFH and PFF) were synthesized by Stille polycondensation of 2,3-diphenyl-5,8-di(thiophen-2-yl)quinoxaline (DTQx) acceptor unit and indacenodithiophene (IDT) donor unit. As films, PHF and PFF comprising two fluoro substituents on the lateral phenyl groups displayed a broad absorption ranging from 350 to 700 nm; whereas PFH containing two fluorine atoms on the polymer main chain exhibited a slightly narrower absorption ranging from 350 to 650 nm. In addition, fluoro substitution on the polymer main chain can lower the HOMO level of the resulted polymers. As expected, PFH and PFF possess deeper HOMO energy level than PHF. Polymer solar cells (PSCs) were fabricated with these three polymers as donor materials and PC71BM as acceptor material. PHF based PSCs gave a power conversion efficiency (PCE) of 7.2% with a Voc of 0.84 V, a Jsc of 12.46 mA/cm2 and an FF of 0.69. And PFH based PSCs showed a PCE of 6.19% with a Voc of 0.93 V, a Jsc of 9.57 mA/cm2 and an FF 0.70. However, a PCE of only 2.9% with a Voc of 0.92 V, a Jsc of 4.61 mA/cm2 and an FF of 0.68 was obtained for PFF based PSCs. Transmission electron microscopy (TEM) and resonant soft X-ray scattering (R-SoXS) studies indicated that the introduction of four fluorine atoms at each repeating unit can spoil the morphology of active layer. These results highlight the importance of fluorination position and number to the performance of PSCs.
Keywords:Polymer solar cells  Fluorination position and number  Morphology
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