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Additive-Free MXene Liquid Crystals and Fibers

Lookup NU author(s): Dr Shayan SeyedinORCiD

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This is the final published version of an article that has been published in its final definitive form by American Chemical Society, 2020.

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Abstract

The discovery of liquid crystalline (LC) phases in dispersions of two-dimensional (2D) materials has enabled the development of macroscopically aligned three-dimensional (3D) macrostructures. Here, we report the first experimental observation of self-assembled LC phases in aqueous Ti₃C₂T_x MXene inks without using LC additives, binders, or stabilizing agents. We show that the transition concentration from the isotropic to nematic phase is influenced by the aspect ratio of MXene flakes. The formation of the nematic LC phase makes it possible to produce fibers from MXenes using a wet-spinning method. By changing the Ti₃C₂T_x flake size in the ink formulation, coagulation bath, and spinning parameters, we control the morphology of the MXene fibers. The wet-spun Ti₃C₂T_x fibers show a high electrical conductivity of ∼7750 S cm^–1, surpassing existing nanomaterial-based fibers. A high volumetric capacitance of ∼1265 F cm^–3 makes Ti₃C₂T_x fibers promising for fiber-shaped supercapacitor devices. We also show that Ti₃C₂T_x fibers can be used as heaters. Notably, the nematic LC phase can be achieved in other MXenes (Mo₂Ti₂C₃T_x and Ti₂CT_x) and in various organic solvents, suggesting the widespread LC behavior of MXene inks.

Publication metadata

Author(s): Zhang J, Uzun S, Seyedin S, Lynch PA, Akuzum B, Wang Z, Qin S, Alhabeb M, Shuck CE, Lei W, Kumbur EC, Yang W, Wang X, Dion G, Razal JM, Gogotsi Y

Publication type: Article

Publication status: Published

Journal: ACS Central Science

Year: 2020

Volume: 6

Issue: 2

Pages: 254-265

Print publication date: 26/02/2020

Online publication date: 06/02/2020

Acceptance date: 16/01/2020

Date deposited: 08/07/2020

ISSN (electronic): 2374-7951

Publisher: American Chemical Society

URL: https://doi.org/10.1021/acscentsci.9b01217

DOI: 10.1021/acscentsci.9b01217

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