TPD-Based Copolymers with Strong Interchain Aggregation and High Hole Mobility for Efficient Bulk Heterojunction Solar Cells
- Authors
- Cheon, Ye Rim; Kim, Yu Jin; Ha, Jong-jin; Kim, Myeong-Jong; Park, Chan Eon; Kim, Yun-Hi
- Issue Date
- Dec-2014
- Publisher
- American Chemical Society
- Citation
- Macromolecules, v.47, no.24, pp 8570 - 8577
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Macromolecules
- Volume
- 47
- Number
- 24
- Start Page
- 8570
- End Page
- 8577
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18581
- DOI
- 10.1021/ma501888z
- ISSN
- 0024-9297
1520-5835
- Abstract
- ADA conjugated polymer, PTPD-TVT, containing thienopyrroledione and thiophenevinylenethiophene (TVT) units was synthesized as an electron donor for organic photovoltaic devices. It possesses a small bandgap and has excellent coplanarity and high hole mobility. To further enhance the interchain interactions between the polymer chains, a selenophenevinyleneselenophene (SVS) unit was also introduced and copolymerized to form the PTPD-SVS polymer. Devices made from PTPD-TVT and PTPD-SVS have rather promising power conversion efficiencies (PCEs) of 4.87 and 5.74%, respectively. The higher PCE value for solar cells based on PTPD-SVS was attributed to an enhanced carrier mobility resulting from stronger interchain aggregation in the BHJ active layer. These results show that the incorporation of a vinylene unit in TPD-based polymers is an effective way to reduce the bandgap and thereby improve charge transport for efficient photovoltaic devices.
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