2,1,3-benzothiadiazole-5,6-dicarboxylicimide based semicrystalline polymers for photovoltaic cells
Autor: | Thanh Luan Nguyen, Dat Thanh Truong Nguyen, Sungu Hwang, Seyeong Song, Mohammad Afsar Uddin, Taehyo Kim, Jin Young Kim, Yuxiang Li, Han Young Woo |
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Rok vydání: | 2016 |
Předmět: |
chemistry.chemical_classification
Electron mobility Fullerene Materials science Polymers and Plastics Band gap Organic Chemistry Energy conversion efficiency 02 engineering and technology Polymer 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Crystallinity chemistry Chemical physics Polymer chemistry Materials Chemistry Charge carrier 0210 nano-technology Current density |
Zdroj: | Journal of Polymer Science Part A: Polymer Chemistry. 54:3826-3834 |
ISSN: | 0887-624X |
Popis: | Two semicrystalline low band gap polymers based on highly electron-deficient 2,1,3-benzothiadiazole-5,6-dicarboxylicimide (BTI) were synthesized by considering the chain planarity via intrachain noncovalent coulombic interactions. The thiophene-BTI and thienothiophene-BTI based PPDTBTI and PPDTTBTI have a low band gap (∼1.5 eV) via strong intramolecular charge transfer interaction, showing a broad light absorption covering 300∼850 nm. Semicrystalline film morphology was observed for both polymers in the grazing incidence wide angle X-ray scattering measurements. Interestingly, PPDTBTI showed a pronounced edge on packing structure but PPDTTBTI showed predominantly a face on orientation in both pristine and blend films. Different packing patterns influenced significantly the charge carrier transport, recombination and resulting photovoltaic characteristics. The best power conversion efficiency was measured to be 5.47% for PPDTBTI and 6.78% for PPDTTBTI, by blending with the fullerene derivative, PC71BM. Compared to the PPDTBTI blend, PPDTTBTI: PC71BM suffered from the lower open-circuit voltage but showed the substantially higher hole mobility and short-circuit current density with smaller charge recombination, showing very good agreements with molecular structures and morphological characteristics. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 |
Databáze: | OpenAIRE |
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