Author
Listed:
- Xiaoyu Li
(School of Chemistry, University of Bristol
Present address: Department of Polymer Materials, School of Material Science and Technology, Beijing Institute of Technology, Beijing 100081, China)
- Piotr J. Wolanin
(School of Chemistry, University of Bristol
Bristol Centre for Functional Nanomaterials, University of Bristol)
- Liam R. MacFarlane
(School of Chemistry, University of Bristol)
- Robert L. Harniman
(School of Chemistry, University of Bristol)
- Jieshu Qian
(School of Chemistry, University of Bristol
Present address: School of Environmental and Biological Engineering, Nanjing University of Science and Technology, 200 Xiao Ling Wei, Nanjing 210094, China)
- Oliver E. C. Gould
(School of Chemistry, University of Bristol
Bristol Centre for Functional Nanomaterials, University of Bristol)
- Thomas G. Dane
(European Synchrotron Radiation Facility)
- John Rudin
(Folium Optics Ltd)
- Martin J. Cryan
(University of Bristol)
- Thomas Schmaltz
(Laboratory of Macromolecular and Organic Materials, Institute of Materials, Ecole Polytechnique Fédérale de Lausanne (EPFL), EPFL–STI–IMX–LMOM)
- Holger Frauenrath
(Laboratory of Macromolecular and Organic Materials, Institute of Materials, Ecole Polytechnique Fédérale de Lausanne (EPFL), EPFL–STI–IMX–LMOM)
- Mitchell A. Winnik
(University of Toronto)
- Charl F. J. Faul
(School of Chemistry, University of Bristol)
- Ian Manners
(School of Chemistry, University of Bristol)
Abstract
Micelles formed by the self-assembly of block copolymers in selective solvents have attracted widespread attention and have uses in a wide variety of fields, whereas applications based on their electronic properties are virtually unexplored. Herein we describe studies of solution-processable, low-dispersity, electroactive fibre-like micelles of controlled length from π-conjugated diblock copolymers containing a crystalline regioregular poly(3-hexylthiophene) core and a solubilizing, amorphous regiosymmetric poly(3-hexylthiophene) or polystyrene corona. Tunnelling atomic force microscopy measurements demonstrate that the individual fibres exhibit appreciable conductivity. The fibres were subsequently incorporated as the active layer in field-effect transistors. The resulting charge carrier mobility strongly depends on both the degree of polymerization of the core-forming block and the fibre length, and is independent of corona composition. The use of uniform, colloidally stable electroactive fibre-like micelles based on common π-conjugated block copolymers highlights their significant potential to provide fundamental insight into charge carrier processes in devices, and to enable future electronic applications.
Suggested Citation
Xiaoyu Li & Piotr J. Wolanin & Liam R. MacFarlane & Robert L. Harniman & Jieshu Qian & Oliver E. C. Gould & Thomas G. Dane & John Rudin & Martin J. Cryan & Thomas Schmaltz & Holger Frauenrath & Mitche, 2017.
"Uniform electroactive fibre-like micelle nanowires for organic electronics,"
Nature Communications, Nature, vol. 8(1), pages 1-9, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15909
DOI: 10.1038/ncomms15909
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Cited by:
- Michael D. Dore & Muhammad Ghufran Rafique & Tianxiao Peter Yang & Marlo Zorman & Casey M. Platnich & Pengfei Xu & Tuan Trinh & Felix J. Rizzuto & Gonzalo Cosa & Jianing Li & Alba Guarné & Hanadi F. S, 2024.
"Heat-activated growth of metastable and length-defined DNA fibers expands traditional polymer assembly,"
Nature Communications, Nature, vol. 15(1), pages 1-13, December.
- Huanzhi Yang & Yunjun Luo & Bixin Jin & Shumeng Chi & Xiaoyu Li, 2024.
"Convoluted micellar morphological transitions driven by tailorable mesogenic ordering effect from discotic mesogen-containing block copolymer,"
Nature Communications, Nature, vol. 15(1), pages 1-10, December.
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