Assembly of poly-3-(hexylthiophene) nanocrystals in marginal solvent: The role of PCBM

Marta Da Pian, Michele Maggini, G. Julius Vancso, Valerio Causin, Edmondo M. Benetti (Corresponding Author)

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Abstract

Poly-3-(hexyl thiophene) (P3HT) represents the benchmark semiconducting polymer for the fabrication of organic photovoltaics (OPVs), where it acts as electron donor component in combination with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), as electron acceptor counterpart. The assembly of P3HT under marginal solvent conditions to form dispersions of fibrillar nanocrystals (NCs) is a particularly attractive method for the subsequent fabrication of highly crystalline films, if compared to depositions involving polymer solutions followed by relatively harsh thermal/solvent treatments, which are often incompatible with sensitive substrates. However, the mechanisms that drive the assembly of P3HT to NCs in marginal solvents are not fully understood, while the effects induced by the presence of PCBM during polymer assembly are still debated. In order to shed light into these processes, we systematically investigated the aggregation/crystallization behaviour of P3HT to NCs under different marginal-solvent conditions and in the presence of different relative contents of PCBM. The starting concentration of P3HT was shown to influence assembly kinetics, the micro-/nano-morphology and the photophysical properties of the formed NCs, as demonstrated by combining atomic force microscopy (AFM) and UV–vis adsorption spectroscopy. Polymer assembly to NCs was also highly dependent on the relative concentration of PCBM, within P3HT:PCBM mixtures typically applied in OPVs. In particular, the combination of UV–vis, AFM and wide-angle X-ray scattering (WAXD) highlighted that PCBM confined the aggregation/crystallization process of P3HT NCs, allowing the formation of extended crystallites, while at high concentrations it hindered the formation of NCs slowing down their assembly.

Original languageEnglish
Pages (from-to)222-228
Number of pages7
JournalEuropean polymer journal
Volume109
DOIs
Publication statusPublished - 1 Dec 2018

Fingerprint

Thiophenes
Butyric acid
Butyric Acid
butyric acid
Thiophene
thiophenes
Nanocrystals
esters
Esters
nanocrystals
assembly
polymers
Crystallization
Atomic force microscopy
Polymers
Agglomeration
atomic force microscopy
crystallization
Semiconducting polymers
Fabrication

Keywords

  • UT-Hybrid-D
  • Nanocrystals
  • Poly-3-(hexyl thiophene)
  • Polymer crystallization
  • X-ray scattering
  • Atomic force microscopy

Cite this

Da Pian, Marta ; Maggini, Michele ; Vancso, G. Julius ; Causin, Valerio ; Benetti, Edmondo M. / Assembly of poly-3-(hexylthiophene) nanocrystals in marginal solvent : The role of PCBM. In: European polymer journal. 2018 ; Vol. 109. pp. 222-228.
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abstract = "Poly-3-(hexyl thiophene) (P3HT) represents the benchmark semiconducting polymer for the fabrication of organic photovoltaics (OPVs), where it acts as electron donor component in combination with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), as electron acceptor counterpart. The assembly of P3HT under marginal solvent conditions to form dispersions of fibrillar nanocrystals (NCs) is a particularly attractive method for the subsequent fabrication of highly crystalline films, if compared to depositions involving polymer solutions followed by relatively harsh thermal/solvent treatments, which are often incompatible with sensitive substrates. However, the mechanisms that drive the assembly of P3HT to NCs in marginal solvents are not fully understood, while the effects induced by the presence of PCBM during polymer assembly are still debated. In order to shed light into these processes, we systematically investigated the aggregation/crystallization behaviour of P3HT to NCs under different marginal-solvent conditions and in the presence of different relative contents of PCBM. The starting concentration of P3HT was shown to influence assembly kinetics, the micro-/nano-morphology and the photophysical properties of the formed NCs, as demonstrated by combining atomic force microscopy (AFM) and UV–vis adsorption spectroscopy. Polymer assembly to NCs was also highly dependent on the relative concentration of PCBM, within P3HT:PCBM mixtures typically applied in OPVs. In particular, the combination of UV–vis, AFM and wide-angle X-ray scattering (WAXD) highlighted that PCBM confined the aggregation/crystallization process of P3HT NCs, allowing the formation of extended crystallites, while at high concentrations it hindered the formation of NCs slowing down their assembly.",
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Assembly of poly-3-(hexylthiophene) nanocrystals in marginal solvent : The role of PCBM. / Da Pian, Marta; Maggini, Michele; Vancso, G. Julius; Causin, Valerio; Benetti, Edmondo M. (Corresponding Author).

In: European polymer journal, Vol. 109, 01.12.2018, p. 222-228.

Research output: Contribution to journalArticleAcademicpeer-review

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T1 - Assembly of poly-3-(hexylthiophene) nanocrystals in marginal solvent

T2 - The role of PCBM

AU - Da Pian, Marta

AU - Maggini, Michele

AU - Vancso, G. Julius

AU - Causin, Valerio

AU - Benetti, Edmondo M.

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PY - 2018/12/1

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AB - Poly-3-(hexyl thiophene) (P3HT) represents the benchmark semiconducting polymer for the fabrication of organic photovoltaics (OPVs), where it acts as electron donor component in combination with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), as electron acceptor counterpart. The assembly of P3HT under marginal solvent conditions to form dispersions of fibrillar nanocrystals (NCs) is a particularly attractive method for the subsequent fabrication of highly crystalline films, if compared to depositions involving polymer solutions followed by relatively harsh thermal/solvent treatments, which are often incompatible with sensitive substrates. However, the mechanisms that drive the assembly of P3HT to NCs in marginal solvents are not fully understood, while the effects induced by the presence of PCBM during polymer assembly are still debated. In order to shed light into these processes, we systematically investigated the aggregation/crystallization behaviour of P3HT to NCs under different marginal-solvent conditions and in the presence of different relative contents of PCBM. The starting concentration of P3HT was shown to influence assembly kinetics, the micro-/nano-morphology and the photophysical properties of the formed NCs, as demonstrated by combining atomic force microscopy (AFM) and UV–vis adsorption spectroscopy. Polymer assembly to NCs was also highly dependent on the relative concentration of PCBM, within P3HT:PCBM mixtures typically applied in OPVs. In particular, the combination of UV–vis, AFM and wide-angle X-ray scattering (WAXD) highlighted that PCBM confined the aggregation/crystallization process of P3HT NCs, allowing the formation of extended crystallites, while at high concentrations it hindered the formation of NCs slowing down their assembly.

KW - UT-Hybrid-D

KW - Nanocrystals

KW - Poly-3-(hexyl thiophene)

KW - Polymer crystallization

KW - X-ray scattering

KW - Atomic force microscopy

U2 - 10.1016/j.eurpolymj.2018.09.049

DO - 10.1016/j.eurpolymj.2018.09.049

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