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Updated: Apr 21, 2026

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Decohesion kinetics in polymer organic solar cells.
Christopher Bruner1, Fernando Novoa, Stephanie Dupont
1Department of Materials Science and Engineering, Stanford University , 496 Lomita Mall, Durand Building, Stanford, California 94305-2205, United States.
Higher molecular weight poly(3-hexylthiophene) improves bulk heterojunction organic solar cell reliability by resisting decohesion. Temperature influences failure mechanisms, impacting device performance and longevity.
Area of Science:
- Materials Science
- Polymer Science
- Renewable Energy
Background:
- Organic solar cells (OSCs) performance is limited by degradation mechanisms.
- Poly(3-hexylthiophene) (P3HT) molecular weight (MW) affects charge transport and morphology.
- Bulk heterojunction (BHJ) layer integrity is crucial for device stability.
Purpose of the Study:
- To investigate the impact of P3HT MW on decohesion kinetics in BHJ OSCs.
- To understand temperature-dependent failure mechanisms in OSCs.
- To correlate P3HT MW with resistance to mechanical failure.
Main Methods:
- Controlled variation of P3HT molecular weight in BHJ OSCs.
- Mechanical testing under inert conditions at various temperatures.
- Development of a viscoelastic model for decohesion analysis.
Main Results:
- Increased P3HT MW enhances resistance to decohesion.
- The BHJ layer consistently fails as the weakest component.
- Below glass transition temperature, brittle failure occurs; above, viscoelastic deformation dominates.
Conclusions:
- P3HT MW is a critical factor for OSC mechanical reliability.
- Temperature-dependent viscoelastic behavior governs decohesion above the glass transition temperature.
- Understanding these failure mechanisms is key for developing durable OSCs.
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