Author
Listed:
- Zhen Chen
(School of Engineering, The University of Tokyo
RIKEN Center for Emergent Matter Science)
- Yi-Tsu Chan
(School of Engineering, The University of Tokyo
RIKEN Advanced Science Institute)
- Daigo Miyajima
(RIKEN Center for Emergent Matter Science
RIKEN SPring-8 Center)
- Takashi Kajitani
(RIKEN Advanced Science Institute
Chemical Resources Laboratory, Tokyo Institute of Technology)
- Atsuko Kosaka
(RIKEN Advanced Science Institute
Chemical Resources Laboratory, Tokyo Institute of Technology)
- Takanori Fukushima
(RIKEN Advanced Science Institute
Chemical Resources Laboratory, Tokyo Institute of Technology)
- Jose M. Lobez
(School of Engineering, The University of Tokyo
RIKEN Advanced Science Institute)
- Takuzo Aida
(School of Engineering, The University of Tokyo
RIKEN Center for Emergent Matter Science
RIKEN Advanced Science Institute)
Abstract
How to orient polymers homeotropically in thin films has been a long-standing issue in polymer science because polymers intrinsically prefer to lie down. Here we provide a design principle for polymers that are processable into a 2D homeotropic order. The key to this achievement was a recognition that cylindrical polymers can be designed to possess oppositely directed local dipoles in their cross-section, which possibly force polymers to tightly connect bilaterally, affording a 2D rectangular assembly. With a physical assistance of the surface grooves on Teflon sheets that sandwich polymer samples, homeotropic ordering is likely nucleated and gradually propagates upon hot-pressing towards the interior of the film. Consequently, the 2D rectangular lattice is constructed such that its b axis (side chains) aligns along the surface grooves, while its c axis (polymer backbone) aligns homeotropically on a Teflon sheet. This finding paves the way to molecularly engineered 2D polymers with anomalous functions.
Suggested Citation
Zhen Chen & Yi-Tsu Chan & Daigo Miyajima & Takashi Kajitani & Atsuko Kosaka & Takanori Fukushima & Jose M. Lobez & Takuzo Aida, 2016.
"A design principle of polymers processable into 2D homeotropic order,"
Nature Communications, Nature, vol. 7(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13640
DOI: 10.1038/ncomms13640
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