Abstract

The dielectric behavior of alkylcyanobiphenyls (5CB and 8CB) confined in porous matrices with randomly oriented, interconnected pores with two different mean pore sizes (1000 and 100 \AA{}) has been investigated by means of broadband dielectric spectroscopy in the frequency range from 1 mHz to 1.5 GHz. The confinement has a strong influence on the dielectric properties of liquid crystals (LCs), which resulted in the appearance of a low frequency relaxation process $(f<~$ 10 kHz) not present in bulk and a second new process due to the presence of surface layer at solid pore wall-LC interface. Bulklike relaxation processes due to the rotation of molecules around the short axis and due to tumbling of molecules are also observed. All observed relaxation processes are of non-Debye type. Other observed differences between bulk and confined behavior are as follows: (a) the relaxation processes in confined LCs are not frozen even at temperatures about 20 degrees below the bulk crystallization temperature; (b) in the temperature range corresponding to the anisotropic phase in pores, the temperature dependence of the relaxation times $(\ensuremath{\tau})$ of the process due to the rotation of molecules around the short axis is non-Arrhenius; (c) the retardation factor $g=\ensuremath{\tau}/{\ensuremath{\tau}}_{\mathrm{is}}$ is $\ensuremath{\simeq}1.5,$ whereas the typical value of $g$ in bulk nematic LCs is $\ensuremath{\simeq}4.$ At the nematic-isotropic phase transition in pores smooth and small changes in $\ensuremath{\tau}$ suggest that the "isotropic" phase of LCs in pores is not bulklike isotropic phase with complete disorder in molecular orientations, and some degree of orientational order still persists.

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