Structure and Nonlinear Index of Refraction of Sunset Yellow Lyotropic Chromonic Liquid Crystal in the Isotropic and Nematic Phases

TL;DR

This study investigates the nonlinear optical properties of sunset yellow lyotropic chromonic liquid crystals, measuring the nonlinear refractive index in different phases and conditions, revealing how molecular aggregation and phase order influence nonlinear optical responses.

Contribution

It extends nonlinear optics research to chromonic liquid crystals, providing new measurements of nonlinear refractive indices and their dependence on phase, concentration, and temperature.

Findings

Nonlinear refractive index $n_2$ doubles with increased concentration.

$n_{2,fast}$ is higher in the nematic phase than in isotropic phase at the same concentration.

$n_{2,fast}$ depends linearly on temperature.

Abstract

Lyotropic chromonic liquid crystals are formed by the self-assembly of aromatic compounds in concentrated solutions. Despite numerous applications of chromonic systems in optical and photonic devices, they all make use of the anisotropic linear optical properties of the nematic or columnar liquid crystalline phases. This paper extends the investigations of chromonic systems to the domain of nonlinear optics. For this purpose, the magnitude and sign of the nonlinear refractive indices, $n_2,$ were measured by the nonlinear ellipse rotation (NER) technique. This was performed on aqueous solutions of sunset yellow azo dye, the prototypical chromonic system. Samples with different concentrations and temperatures were used, both in the isotropic and nematic phases. In addition, the molecular aggregation states of the chromonic samples as a function of temperature and concentration were investigated by wide angle X-ray scattering. NER measurements as a function of the laser pulse width from $65\,fs$ to $\sim 5\,ps$ allowed the decomposition of $n_2$ into a fast contribution, $n_{2,fast},$ associated with molecular electronic processes, and a slow one $n_{2,slow},$ associated with molecular reorientational processes. It was shown that $n_{2,fast}$ doubled from the isotropic phases of the $15$ to the $30\,\%\,\text{w/w}$ samples, proportionally to the increase in mass fraction. However, $n_{2,fast}$ for the aligned nematic phase of $30\,\%\,\text{w/w}$ sample was higher than the double of the corresponding value for the $15\,\%\,\text{w/w}$ sample, showing an effect associated to the orientational order of this phase. Also, $n_{2,fast}$ was shown to depend linearly on temperature.