4.8 Article

Pyridine End-Capped Polymer to Stabilize Organic Nanoparticle Dispersions for Solar Cell Fabrication through Reversible Pyridinium Salt Formation

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 30, Pages 36044-36052

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07219

Keywords

poly(3-hexylthiophene); end-capped polymer; nanoparticle dispersion; bulk-heterojunction; organic solar cells

Funding

  1. Australian Renewable Energy Agency (ARENA) within the Australian Centre for Advanced Photovoltaics (ACAP)
  2. German Federal Ministry for Education and Research [03EK3571]
  3. ARC Centre of Excellence in Exciton Science [CE170100026]

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The stability of P3HT:indene-C-60 bis-adduct (ICBA) nanoparticle dispersions is enhanced by incorporating pyridine end-capped poly(3-hexylthiophene) (P3HT-Py) as an additive, allowing for smaller nanoparticle sizes and higher concentrations. This approach results in improved shelf-life and performance of the solar cells with a minimal impact on device efficiency.
Bulk-heterojunction nanoparticle dispersions in water or alcohol can be employed as eco-friendly inks for the fabrication of organic solar cells by printing or coating. However, one major drawback is the need for stabilizing surfactants, which facilitate nanoparticle formation but later hamper device performance. When surfactant-free dispersions are formulated, a strong limitation is imposed by the dispersion concentration due to the tendency of nanoparticles to aggregate. In this work, pyridine end-capped poly(3-hexylthiophene) (P3HT-Py) is synthesized and included as an additive for the stabilization of P3HT:indene-C-60 bis-adduct (ICBA) nanoparticle dispersions. In the presence of acetic acid (AcOH), a surface-active pyridinium acetate end-capped P3HT ion pair, P3HT-PyH+AcO-, is formed which effectively stabilizes the dispersion and hence allows the formation of dispersions with smaller nanoparticle sizes and higher concentrations of up to 30 mg/mL in methanol. The dispersions exhibit an enhanced shelf-lifetime of at least 60 days at room temperature. After the deposition of light-harvesting layers from the nanoparticle dispersions, the ion-pair formation is reversed at elevated temperatures leading to regeneration of P3HT-Py and AcOH. The AcOH evaporates from the active layer, while the performance of the corresponding solar cells is not affected by the residual P3HT-Py in the devices. Enhanced nanoparticle stability is achieved with only 0.017 wt % pyridine in the P3HT/ICBA formulation.

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