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Updated: Feb 17, 2026

Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization
Published on: January 29, 2017
Tuning Intermolecular Interactions With Solid Additives to Optimize Molecular Aggregation and Molecular Packing in
Luzhuo Li1,2, Hanyue Gao1,2, Yu Shen1,2
1State Key Laboratory of Polymer Science and Technology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, China.
Volatile solid additives improve polymer compatibility in all-polymer solar cells (all-PSCs) by regulating aggregation and phase separation. This strategy enhances power conversion efficiency by optimizing film morphology.
Area of Science:
- Materials Science
- Polymer Chemistry
- Renewable Energy
Background:
- All-polymer solar cells (all-PSCs) face challenges with polymer aggregation and phase separation, limiting performance.
- Poor compatibility between donor and acceptor polymers is a key issue in all-PSC development.
Purpose of the Study:
- To introduce volatile solid additives for controlling aggregation and phase separation in all-PSCs.
- To investigate the role of electrostatic interactions in modulating polymer blend miscibility and morphology.
Main Methods:
- Computational modeling and experimental characterization were employed.
- Volatile solid additives were incorporated into the polymer blend during film fabrication.
- Morphology evolution and intermolecular interactions were analyzed.
Main Results:
- Strong electrostatic potential coupling between the additive and polymer acceptor was identified as crucial.
- The additive effectively reduced aggregate size and enhanced molecular packing.
- All-PSCs with the additive achieved a power conversion efficiency of 18.62%, up from 14.93%.
Conclusions:
- Engineered electrostatic interactions via solid additives offer a viable strategy for optimizing all-PSC morphology.
- This approach successfully addresses polymer aggregation and phase separation issues.
- The study demonstrates a significant performance enhancement in all-PSCs through controlled intermolecular forces.
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