Green solvent-processable poly(3-hexylthiophene) derivative maintains high hole mobility in diodes

The development of environmentally sustainable fabrication methods for organic solar cells (OSCs) is critical to enable their large-scale adoption. Conventional solution-processed OSCs often rely on halogenated, toxic solvents that pose health and environmental risks, limiting their scalability. This is because π-conjugated polymers tend to have a low solubility in non-halogenated solvents. A common strategy to enhance solubility in alternative solvents is through the incorporation of polar solubilizing groups, often on every repeat unit of at least one monomer. However, too many polar side chains tend to disrupt favorable morphology and decrease charge transport properties. In this study, we demonstrate that a minimal degree of side chain functionalization can improve green solvent processability while preserving electrical performance. We tested this hypothesis using our previously reported random copolymer derivative of poly(3-hexylthiophene) (P3HT) where ∼10 mol% of the side chains are 6-pentanoatehexyl side chains. We find that this low-level functionalization significantly broadens the solvents that can be used to process P3HT to less toxic solvents such as o -xylene and anisole. Furthermore, the copolymer processed from greener solvents showed high hole mobilities (∼10⁻ 3 cm 2 /Vs by the Space-Charge Limiting Current method in diodes), comparable to P3HT films cast from toxic chloroform. These findings suggest that minimal side-chain modification is a viable strategy for expanding green solvent compatibility while preserving electrical performance, paving the way toward more sustainable organic semiconductor designs. • Conventional solution-processing on P3HT uses toxic chlorinated solvents. • We tested a random copolymer of P3HT with 10 mol% 6-pentanoatehexyl side chains. • Minimal side-chain changes expanded green solvent processing of P3HT. • The morphology and crystallinity were preserved using the less toxic solvents. • Films processed from the greener solvents maintain a high hole mobility.

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Publication Details

Journal
Synthetic Metals
Published
2025-08-12
DOI
https://doi.org/10.1016/j.synthmet.2025.117940
Primary Topic
Organic Electronics and Photovoltaics
Type
article
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article

Green solvent-processable poly(3-hexylthiophene) derivative maintains high hole mobility in diodes

Quynh Tran, Lei Zhu, Lexi R. Knight, Geneviève Sauvé et al.
Synthetic Metals
Organic Electronics and Photovoltaics
article

Green solvent-processable poly(3-hexylthiophene) derivative maintains high hole mobility in diodes

Quynh Tran, Lei Zhu, Lexi R. Knight, Geneviève Sauvé, Honghu Zhang, Maia M. Tritt
article en

Abstract

The development of environmentally sustainable fabrication methods for organic solar cells (OSCs) is critical to enable their large-scale adoption. Conventional solution-processed OSCs often rely on halogenated, toxic solvents that pose health and environmental risks, limiting their scalability. This is because π-conjugated polymers tend to have a low solubility in non-halogenated solvents. A common strategy to enhance solubility in alternative solvents is through the incorporation of polar solubilizing groups, often on every repeat unit of at least one monomer. However, too many polar side chains tend to disrupt favorable morphology and decrease charge transport properties. In this study, we demonstrate that a minimal degree of side chain functionalization can improve green solvent processability while preserving electrical performance. We tested this hypothesis using our previously reported random copolymer derivative of poly(3-hexylthiophene) (P3HT) where ∼10 mol% of the side chains are 6-pentanoatehexyl side chains. We find that this low-level functionalization significantly broadens the solvents that can be used to process P3HT to less toxic solvents such as o -xylene and anisole. Furthermore, the copolymer processed from greener solvents showed high hole mobilities (∼10⁻ 3 cm 2 /Vs by the Space-Charge Limiting Current method in diodes), comparable to P3HT films cast from toxic chloroform. These findings suggest that minimal side-chain modification is a viable strategy for expanding green solvent compatibility while preserving electrical performance, paving the way toward more sustainable organic semiconductor designs. • Conventional solution-processing on P3HT uses toxic chlorinated solvents. • We tested a random copolymer of P3HT with 10 mol% 6-pentanoatehexyl side chains. • Minimal side-chain changes expanded green solvent processing of P3HT. • The morphology and crystallinity were preserved using the less toxic solvents. • Films processed from the greener solvents maintain a high hole mobility.

Synthetic MetalsVol. 314
Brookhaven National Laboratory (US), Case Western Reserve University (US)
Affordable and clean energy
Openalex Percentile: Top 81%
Organic Electronics and Photovoltaics
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