Abstract
The present manuscript reports the design, synthesis and characterization of three star-shaped polymers consisting of three different arylimides such as perylene (PR)-, naphthalene (NT)- and benzene (BZ) tetracarboxylicdiimide as core and polyfluorene (PF) as arms. Chemical structure of star-shaped polymers was aimed at broadening as much as possible their absorption profile. Arylimide cored star polymers (PF-BZ, PF-NT and PF-PR) were prepared through palladium catalyzed Suzuki polycondensation to tune the band gap of the polymers. The prepared polymers were characterized by elemental analysis, NMR, GPC, UV–Vis, photoluminescence and cyclic voltammetry studies. Electrochemical and optical responses of three polymers revealed the lowering of band gap from linear PF to star-shaped polymers. TCSPC study confirmed the partial energy transfer from PF arms to arylimide cores. The unexpected keto defect in linear PF was also reduced by preparation of star polymer with large arylimide cores. TGA exhibited the enhancement of thermal stability of star polymer than linear PF. By using star polyfluorenes as the donor and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) as the acceptor, bulk heterojunction (BHJ) solar cells of the structure ITO/PEDOT:PSS/star polymer: PCBM/Al were fabricated and studied with a solar simulator under AM1.5G (100mW/cm2) irradiation intensity. Those cells showed the open circuit voltage (Voc) ∼0.52–0.55V, the short circuit current density (Jsc) ∼0.84–1.13mAcm−2, the fill factor ∼0.39–0.44 and the power conversion efficiency (PCE) ∼0.18–0.26%.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.