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Synthesis and characterization of diselenenoquinoxaline-based donor–acceptor polymers for organic photovoltaic cells
- Source :
- Synthetic Metals. 162:873-880
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- Two new conjugated polymers, PQSS and PQST, were designed and synthesized; these polymers had alkylselenophene-substituted quinoxaline backbones with selenophene and thiophene, respectively, as electron-donating units. The copolymers showed good solubility and film forming abilities, combined with good thermal stability. The number-average molecular weights ( M n ) of PQSS and PQST, determined using gel permeation chromatography (GPC) with a polystyrene standard, were found to be 20,900 ( M w / M n = 1.71) and 22,100 ( M w / M n = 2.41), respectively. The UV–visible absorption maxima of PQSS and PQST were at 617 and 601 nm in solution, and at 682 and 668 nm in the film state. The PQSS and PQST showed low band gaps of 1.50 and 1.52 eV, respectively. Solution-processed field-effect transistors fabricated from these polymers had p-type organic thin film transistor characteristics. The field-effect mobilities of PQSS and PQST were measured to be 1.4 × 10 −4 and 4.8 × 10 −5 cm 2 V −1 s −1 , respectively. The polymers were combined with a PC 71 BM ([6,6]-phenyl C 71 -butyric acid methyl ester) acceptor to fabricate bulk heterojunction solar cells, which produced power conversion efficiencies of 0.40–1.07% under AM 1.5G (100 mW/cm 2 ) conditions.
- Subjects :
- chemistry.chemical_classification
Materials science
Organic solar cell
Mechanical Engineering
Metals and Alloys
Analytical chemistry
Polymer
Condensed Matter Physics
Acceptor
Polymer solar cell
Electronic, Optical and Magnetic Materials
Gel permeation chromatography
chemistry.chemical_compound
chemistry
Mechanics of Materials
Polymer chemistry
Materials Chemistry
Thiophene
Thermal stability
Polystyrene
Subjects
Details
- ISSN :
- 03796779
- Volume :
- 162
- Database :
- OpenAIRE
- Journal :
- Synthetic Metals
- Accession number :
- edsair.doi...........9c6c2d7c9e6927a8ef7b34cf4967efc7
- Full Text :
- https://doi.org/10.1016/j.synthmet.2012.03.022