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Updated: Sep 27, 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
Suppressing Molecular Aggregation via Alkyl Chain Steric Hindrance Enabled High-Performance Self-Assembly
Wei Tang1,2, Huizhen Xu3, Lei Wu3
1School of Chemistry and Environmental Science, Xiangnan University, Chenzhou423000, P. R. China.
Abstract:
Interfacial inhomogeneity and carrier recombination caused by molecular aggregation in self-assembled monolayers (SAMs) remain critical challenges for organic solar cells. Herein, we report an interfacial engineering strategy utilizing octylphosphonic acid (8PA) as a morphology-modulating additive. By blending 8PA with [4-(3,6-diphenyl-9H-carbazol-9-yl)butyl]phosphonic acid (Ph-4PACz), we achieve molecular-level miscibility via compatible phosphonic acid anchoring groups, while the extended alkyl chain of 8PA introduces steric hindrance that effectively suppresses π-π molecular aggregation. Experimental results demonstrate that this strategy significantly inhibits the self-agglomeration of Ph-4PACz, thereby enhancing the homogeneity and surface coverage of the resultant monolayer and optimizing molecular ordering. Devices incorporating the 8PA-modified SAM exhibit uniform phase separation morphology, reduced recombination centers, and facilitated charge transport. Consequently, the optimized device achieves a champion power conversion efficiency (PCE) of 19.8%, representing a significant improvement over the 18.2% observed in control devices. This work provides an effective pathway for enhancing the performance of organic photovoltaic devices through additive-driven SAM morphology control.

