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Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Optimizing Active Layer Morphology of Organic Solar Cells by Constructing Random Copolymers with Simple Third Units.
Qian Xie1, Chunyu Qiao1, Jie Fang1
1Institute of Applied Chemistry, Jiangxi Academy of Sciences, Nanchang, 330096, China.
Modifying polymer PM6 with difluoro-thiophene (2FT) units improved crystallinity and organic solar cell performance. Dicyano-thiophene (2CNT) units had the opposite effect, but ternary devices achieved high efficiency.
Area of Science:
- Materials Science
- Polymer Chemistry
- Organic Electronics
Background:
- The performance of organic solar cells (OSCs) is highly dependent on the molecular structure and morphology of the donor polymer.
- Optimizing polymer backbone coplanarity and crystallinity is crucial for efficient charge transport and device efficiency.
Purpose of the Study:
- To investigate the impact of incorporating difluoro-substituted thiophene (2FT) and dicyano-substituted thiophene (2CNT) units into the PM6 polymer backbone via random copolymerization.
- To correlate structural modifications with changes in molecular crystallinity, morphology, charge transport properties, and ultimately, the power conversion efficiency (PCE) of organic solar cells.
Main Methods:
- Random copolymerization of the polymer PM6 with 2FT and 2CNT units.
- Characterization of the resulting copolymers' molecular structure, coplanarity, and crystallinity.
- Fabrication and performance testing of organic solar cells using these modified polymers.
- Analysis of charge carrier mobilities and morphology in the active layers.
Main Results:
- Incorporation of 2FT units enhanced polymer coplanity and molecular crystallinity, leading to improved charge mobilities and a PCE of 12.65% in PM6-10%2FT:IT4F based OSCs.
- Introduction of 2CNT units reduced coplanity and crystallinity, resulting in lower PCEs (<12%) for the 2CN-series random copolymers.
- A ternary device (PM6:L8-BO:PM6-20%2CN) achieved a superior PCE of 19.0% due to enhanced open-circuit voltage.
Conclusions:
- Enhancing the coplanarity of donor polymer backbones through the introduction of specific structural units (like 2FT) can significantly improve molecular crystallinity.
- Optimized polymer crystallinity and backbone coplanity lead to favorable morphology and enhanced charge transport in organic solar cells.
- Strategic molecular design, including the use of ternary blends, offers a promising pathway for achieving high-performance organic solar cells.
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