Ferroelectric behavior of orthogonal smectic phase made of bent-core molecules

Lingfeng Guo, Ewa Gorecka, Damian Pociecha, Nataša Vaupotič, Mojca Čepič, R. Amaranatha Reddy, Kristina Gornik, Fumito Araoka, Noel A. Clark, David M. Walba, Ken Ishikawa, and Hideo Takezoe
Phys. Rev. E 84, 031706 – Published 21 September 2011

Abstract

Ferroelectric behavior in the recently reported orthogonal ferroelectric Sm-AdPF phase in an unsymmetric bent-core molecule with a carbosilane terminal group was studied. The ferroelectricity of the Sm-AdPF phase was unambiguously confirmed by optical second-harmonic generation activity in the absence of an electric field, ferroelectric response, and high dielectric strength. The long-range polar order is a consequence of weakened interlayer coupling due to the formation of carbosilane sublayers, which allows for the parallel order of dipole moments of bent-core molecules in the neighboring layers. It develops in the system gradually through the second-order phase transition from the orthogonal Sm-Ad phase. In the Sm-AdPF phase the strong surface anchoring results in the splay of polarization across the sample thickness. The polar surface anchoring also brings about strongly thickness-dependent polar fluctuations, as proved by the dielectric measurements (Goldstone-like mode). The relaxation frequency and dielectric strength vary more than one order of magnitude with cell thickness; in particular the dielectric strength attains more than 2000 in a 25 μm-thick cell and continues to increase for thicker cells. Simple theory developed qualitatively explains the experimental results, supporting the polarization splay model proposed.

  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
2 More
  • Received 3 July 2011

DOI:https://doi.org/10.1103/PhysRevE.84.031706

©2011 American Physical Society

Authors & Affiliations

Lingfeng Guo1, Ewa Gorecka2, Damian Pociecha2, Nataša Vaupotič3,4, Mojca Čepič4,5, R. Amaranatha Reddy6, Kristina Gornik3,5, Fumito Araoka1, Noel A. Clark7, David M. Walba6, Ken Ishikawa1, and Hideo Takezoe1,*

  • 1Department of Organic and Polymeric Materials, Tokyo Institute of Technology, 2-12-1-S8-42 O-okayama, Meguro-ku, Tokyo 152-8552, Japan
  • 2Chemistry Department,Warsaw University, Al. Zwirki i Wigury 101, PL-02-089 Warsaw, Poland
  • 3Department of Physics, Faculty of Natural Sciences and Mathematics, University of Maribor, Koroska 160, Sl-2000 Maribor, Slovenia
  • 4Jozef Stefan Institute, Jamova 39, Sl-1000 Ljubljana, Slovenia
  • 5Department of Physics and Technology, Faculty of Education, University of Ljubljana, Kardeljeva ploščad 16, Sl-1000 Ljubljana, Slovenia
  • 6Department of Chemistry and Biochemistry, Liquid Crystal Materials Research Center, University of Colorado, Boulder, Colorado 80309-0215, USA
  • 7Department of Physics, Liquid Crystal Materials Research Center, University of Colorado, Boulder, Colorado 80309-0390, USA

  • *takezoe.h.aa@m.titech.ac.jp

Article Text (Subscription Required)

Click to Expand

References (Subscription Required)

Click to Expand
Issue

Vol. 84, Iss. 3 — September 2011

Reuse & Permissions
Access Options
CHORUS

Article Available via CHORUS

Download Accepted Manuscript
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review E

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×