Data-Driven Discovery and Experimental Validation of Solvent Polarity Effects on Conjugated Polymer Solution-to-Film Assembly Pathways
High Resolution Image Download MS PowerPoint Slide Understanding how solvent properties influence the solution-to-film assembly of conjugated polymers remains a critical challenge due to the complex and intertwined nature of polymer–solvent interactions. In this study, we integrate a data-driven framework with experimental validation to identify key parameters influencing the assembly and performance of poly[2,5-(2-octyldodecyl)-3,6-diketopyrrolopyrrole- alt -5,5-(2,5-di(thien-2-yl)thieno[3,2- b ]thiophene)] (DPP-DTT) in organic field-effect transistors (OFETs). A machine learning (ML) approach identified the normalized Reichardt polarity parameter (E T N ) as a significant descriptor correlated with DPP-DTT hole mobility (μ). Systematic DPP-DTT devices fabricated using solvents across a wide E T N range revealed that higher E T N solvents yield enhanced μ. To elucidate the structural origins of high μ, we conducted comprehensive analyses using UV–vis–NIR spectroscopy and grazing incidence wide angle X-ray scattering (GIWAXS) measurements. The results revealed that films processed from high E T N solvents exhibit reduced paracrystallinity. By analyzing the solution-state behavior using optical microscopy and solution WAXS, we revealed polymer solubility differences in the various solvents and associated distinct polymer assembly pathways, elucidating why the high E T N solvent produces long-range ordered films. Notably, the high E T N solvent shows a pronounced preference for liquid-crystal (LC)-mediated assembly, providing a mechanistic explanation for the enhanced structural order. Therefore, these results demonstrate that solvent polarity, as evaluated by E T N, serves as an important parameter that plays a significant role in the DPP-DTT assembly pathway and resultant solid-state morphology. This work provides a strategy for integrating data science with experiments to identify critical parameters associated with complex polymer systems and helps guide rational process design for high-performance organic electronics.
Authors
- Nahyun Ahn (ORCID: https://orcid.org/0000-0003-3737-1617)
- Priyotosh Bairagya (ORCID: https://orcid.org/0000-0002-6912-391X)
- Ying Diao (ORCID: https://orcid.org/0000-0002-8984-0051)
- Elsa Reichmanis (ORCID: https://orcid.org/0000-0002-8205-8016)
- Myeongyeon Lee (ORCID: https://orcid.org/0000-0002-3035-9909)
- Martha A. Grover (ORCID: https://orcid.org/0000-0002-7036-776X)
- Sanghyun Jeon (ORCID: https://orcid.org/0000-0001-8148-9714)
- Azzaya Khasbaatar (ORCID: https://orcid.org/0000-0002-4145-3511)
- Yen-Chi Chen (ORCID: https://orcid.org/0009-0008-2323-9360)
- Chiwon Yu
Institutions
- Georgia Institute of Technology (US)
- University of Illinois Urbana-Champaign (US)
- Lehigh University (US)
Publication Details
- Journal
- Chemistry of Materials
- Published
- 2026-07-16
- DOI
- https://doi.org/10.1021/acs.chemmater.6c00358
- Primary Topic
- Organic Electronics and Photovoltaics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- U.S. Department of Energy
- Lehigh University
- Office of Science
- Multidisciplinary University Research Initiative
- Office of Naval Research
- Division of Materials Research
- Basic Energy Sciences
- Air Force Office of Scientific Research
- Argonne National Laboratory