An alternating copolymer of fluorene donor and quinoxaline acceptor versus a terpolymer consisting of fluorene, quinoxaline and benzothiadiazole building units: synthesis and characterization
Journal article, 2016

An alternating polyfluorene copolymer based on fluorene donor and quinoxaline acceptor (P1) and an alternating terpolymer (P2) with fluorene (50 %) donor and quinoxaline (25 %) and benzothiadiazole (25 %) acceptor units were designed and synthesized for use as photoactive materials in solar cells. The presence of benzothiadiazole unit in P2 increased the optical absorption coverage in the range of 350-600 nm, which is an interesting property and a big potential for achieving improved photovoltaic performances with judicious optimization of the devices. Solar cells were fabricated from 1:4 blends of polymers-PCBM[70] using o-dichlorobenzene (o-DCB) as processing solvent, and P1 showed a power conversion efficiency (PCE) of 3.18 %, with a short-circuit current density (J (SC)) of 7.78 mA/cm(2), an open-circuit voltage (V (OC)) of 0.82 V, and a fill factor (FF) of 50 % while P2 showed an overall PCE of 2.14 % with corresponding J (SC) of 5.97 mA/cm(2), V (OC) of 0.84 V and FF of 42 %. In general, P2 gave lower J (SC) and FF presumably due to the fine domain sizes of the polymer-PCBM[70] blend as seen from the atomic force microscopy (AFM) image which might have affected the charge carrier transport. Alternating (P1) and ternary (P2) conjugated polymers were designed, synthesized and used for fabrication of photovoltaic devices.

Polyfluorenes

Quinoxaline

Fluorene

Suzuki coupling reaction

Benzothiadiazole

Author

Desta Antenehe Gedefaw

Chalmers, Chemistry and Chemical Engineering, Applied Chemistry, Polymer Technology

Z. F. Ma

Linköping University

E. Mulugeta

Addis Ababa University

Y. Zhao

Linköping University

Fengling Zhang

Linköping University

Mats Andersson

Chalmers, Chemistry and Chemical Engineering, Applied Chemistry, Polymer Technology

W. Mammo

Addis Ababa University

Polymer Bulletin

0170-0839 (ISSN) 1436-2449 (eISSN)

Vol. 73 4 1167-1183

Subject Categories

Polymer Chemistry

DOI

10.1007/s00289-015-1541-y

More information

Latest update

2/28/2018