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Articles

Dielectric analysis of the interaction of nematic liquid crystals with carbon nanotubes

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Pages 450-458 | Received 19 Mar 2017, Accepted 20 Jun 2017, Published online: 29 Jun 2017
 

ABSTRACT

Multi-walled carbon nanotubes (MWCNTs) have been shown to self-organise, and when added as a guest to form a nanocomposite, their director couples with an organic liquid crystal (LC) host. Here, effects of MWCNTs on the low-frequency dielectric properties and Fréedericksz transition of the LC 4-cyano-4ʹ-pentylbiphenyl (5CB) are studied. Anti-parallel electro-optic cells were filled with nanocomposites at weight percent concentrations of MWCNT to 5CB of: 0 (neat), 0.01, 0.10, 0.20, and 0.50. Low concentration was chosen to minimise Van der Waals attraction normally responsible for aggregation of MWCNTs. Dielectric relaxation spectroscopy was used to study interactions between MWCNTs and 5CB at frequencies from 20 Hz to 1 MHz. We propose a mechanism based upon measurements of the complex dielectric function which suggests that MWCNTs act as a slow-moving boundary within the sample cell at low frequencies and low applied electric fields, where the MWCNTs reorient along with the 5CB LC molecules. At higher frequencies and larger applied electric fields, the 5CB molecules rotate about their long axes while motion of the MWCNTs is frozen out.

GRAPHICAL ABSTRACT

Acknowledgments

For support of this research, the authors thank the National Science Foundation, Polymers Program of the Division of Materials Research, through DMR 1206010 and DMR 1608125. GG thanks Assumption College for a Faculty Development Grant and financial support and The Natural Science Department at Assumption College. TJA is supported by a Cottrell Award from the Research Corporation for Science Advancement.

Disclosure statement

No potential conflict of interest was reported by the authors.

Supplemental data

Supplemental data for this article can be accessed here.

Additional information

Funding

For support of this research, the authors thank the National Science Foundation, Polymers Program of the Division of Materials Research, through DMR 1206010 and DMR 1608125. GG thanks Assumption College for a Faculty Development Grant and financial support. TJA is supported by a Cottrell Award from the Research Corporation for Science Advancement.

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