Self-Assembly Behavior of an Oligothiophene-Based Conjugated Liquid Crystal and Its Implication for Ionic Conductivity Characteristics

ZW Liu and BX Dong and M Misra and YY Sun and J Strzalka and SN Patel and FA Escobedo and PF Nealey and CK Ober, ADVANCED FUNCTIONAL MATERIALS, 29, 1805220 (2019).

DOI: 10.1002/adfm.201805220

In this work, a joint experimental and computational study on the synthesis, self-assembly, and ionic conduction characteristics of a new conjugated liquid crystal quaterthiophene/poly(ethylene oxide) (PEO4) consisting of terminal tetraethyleneglycol monomethyl ether groups on both ends of a quaterthiophene core is performed. In agreement with molecular dynamic simulations, temperature-dependent grazing-incidence wide angle X-ray scattering and X-ray diffraction indicate that the molecule spontaneously forms a smectic phase at ambient temperature as characterized both in bulk and thin film configurations. Significantly, this smectic phase is maintained upon blending with bis(trifluoro- methanesulfonyl)imide as ion source at a concentration ratio up to r = Li+/EO = 0.05. Nanosegregation between oligothiophene and PEO moieties and pi-pi stacking of thiophene rings lead to the formation of efficient 2D pathways for ion transport, resulting in thin-film in-plane ionic conductivity as high as 5.2 x 10(-4) S cm(-1) at 70 degrees C and r = 0.05 as measured by electrochemical impedance spectroscopy. Upon heating the samples above a transition temperature around 95 degrees C, an isotropic phase forms associated with a pronounced drop in ionic conductivity. Upon cooling, partial and local reordering of the conducting smectic domains leads to an ionic conductivity decrease compared to the as-cast state.

Return to Publications page