4.8 Article

Ion Transport in 2D Nanostructured π-Conjugated Thieno[3,2-b]thiophene-Based Liquid Crystal

Journal

ACS NANO
Volume 16, Issue 12, Pages 20714-20729

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c07789

Keywords

ion conduction; pi-conjugated liquid crystal; molecular dynamics simulation; thin film electrochemical impedance spectroscopy; X-ray diffraction pattern

Funding

  1. NSF DMREF Award [1922259]
  2. U.S. Department of Energy (DOE) [DE-AC02-06CH11357]
  3. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource of the National Science Foundation's National Nanotechnology Coordinated Infrastructure [NSF ECCS-2025633]
  4. National Science Foundation [DMR-2011854, ACI-1053575]
  5. NSF MRSEC program [ACI-1053575]

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Leveraging the self-assembling behavior of liquid crystals for controlling ion transport is of great significance. In this study, a liquid crystal material was designed and prepared, which showed ion-conducting behavior by adding an ion-conducting salt. The material maintained a well-ordered smectic phase within a certain concentration range. The study also found that forming irregular interfaces and expanding the film can enhance ion conduction.
Leveraging the self-assembling behavior of liquid crystals designed for controlling ion transport is of both fundamental and technological significance. Here, we have designed and prepared a liquid crystal that contains 2,5-bis(thien-2-yl)thieno[3,2-b]thiophene (BTTT) as mesogenic core and conjugated segment and symmetric tetra(ethylene oxide) (EO4) as polar side chains for ion-conducting regions. Driven by the crystallization of the BTTT cores, BTTT/dEO4 exhibits well-ordered smectic phases below 71.5 degrees C as confirmed by differential scanning calorimetry, polarized optical microscopy, temperature-dependent wide-angle X-ray scattering, and grazing incidence wideangle X-ray scattering (GIWAXS). We adopted a combination of experimental GIWAXS and molecular dynamics (MD) simulations to better understand the molecular packing of BTTT/dEO4 films, particularly when loaded with the ionconducting salt lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). Ionic conduction of BTTT/dEO4 is realized by the addition of LiTFSI, with the material able to maintain smectic phases up to r = [Li+]/[EO] = 0.1. The highest ionic conductivity of 8 x 10(-3) S/cm was attained at an intermedium salt concentration of r = 0.05. It was also found that ion conduction in BTTT/dEO4 is enhanced by forming a smectic layered structure with irregular interfaces between the BTTT and EO4 layers and by the lateral film expansion upon salt addition. This can be explained by the enhancement of the misalignment and configurational entropy of the side chains, which increase their local mobility and that of the solvated ions. Our molecular design thus illustrates how, beyond the favorable energetic interactions that drive the assembly of ion solvating domains, modulation of entropic effects can also be favorably harnessed to improve ion conduction.

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