4.7 Article

Carbohydrate-attached fullerene derivative for selective localization in ordered carbohydrate-block-poly(3-hexylthiophene) nanodomains

Journal

CARBOHYDRATE POLYMERS
Volume 255, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2020.117528

Keywords

Carbohydrate-based semiconducting block copolymers; Self-assembly; Nanostructured bulk heterojunction; Fullerene derivative; Organic photovoltaics

Funding

  1. SweetMemory International France-Taiwan ANR project [ANR-14-CE08-0021]
  2. Institute Carnot PolyNat ANR [CARN-025-01]
  3. European Union [603519]
  4. JSPS [19H02769]
  5. Photoexcitonix Project (Hokkaido University)
  6. Creative Research Institute (CRIS, Hokkaido University)
  7. ANR under the Investissements d'avenir program [ANR-11-EQPX0010]
  8. CNRS
  9. Grenoble Alpes University

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A carbohydrate-based fullerene derivative was synthesized and applied to a lamellar-forming high-chi block copolymer system to realize an ordered donor/acceptor network. Through thermal annealing, a well-defined D/A lamellar structure with sub-10 nm domain features was achieved. The molecules of the derivative were localized in phase-separated nanodomains without disrupting the lamellar morphology, showing potential for new strategies in blend synthesis.
A carbohydrate-based fullerene derivative (AcMal(7)-C-61) is designed, synthesized and applied to a lamellar-forming high-chi block copolymer system, poly(3-hexylthiophene)-block-peracetylated maltoheptaose (P3HT-b-AcMal(7)), to actualize an ordered donor/acceptor (D/A) network. A well-defined D/A lamellar structure of the P3HT-b-AcMal(7) :AcMal(7)-C-61 blend with sub-10 nm domain features is achieved upon thermal annealing. The AcMal(7)-C-61 molecules are localized in the phase-separated AcMal(7) nanodomains without causing the formation of fullerene crystals while maintaining the lamellar morphology up to 1:0.5 (D:A) blending ratio. The cross-sectional TEM observation and GISAXS measurement reveals that the P3HT-b-AcMal(7) tends to spontaneously organize into lamellar structures oriented perpendicular to the film surface at the air/film interface while the domain orientation at the bottom interface depends on the nature of the substrate.

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