Preparation of Electron/Ion-Mixed Conducting Gel Using Liquid Metal and Ionic Liquid

离子液体 材料科学 化学工程 离子电导率 聚合物 离子键合 热稳定性 离子 复合材料 化学 有机化学 物理化学 电极 电解质 催化作用 工程类
作者
Juri Asada,Aya Saruwatari,Ryota Tamate,Hiroki Ota,Masayoshi Watanabe,Kazuhide Ueno
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2020-02 (59): 2967-2967
标识
DOI:10.1149/ma2020-02592967mtgabs
摘要

Introduction Eutectic gallium-indium (Ga-In) has excellent properties, such as low melting point of 15.3 °C, high thermal and electronic conductivity, and metallic luster. Ga-In has promise as a liquid electron-conducting material owing to its low viscosity, negligible vapor pressure and low toxicity. 1, 2) On the other hand, ionic liquids are ambient temperature molten salts that have attracted considerable attention because of unique properties such as high ionic conductivity, non-volatility and thermal stability. We proposed that ion gels, composed of macromolecular networks swollen with ionic liquids, exhibit self-standing film-forming ability in addition to the unique properties of ionic liquids. In this study, we prepared composite gel materials containing ionic liquid and Ga-In. This composite gel (metal gel) might have high electronic conductivity based on Ga-In and high ionic conductivity originated from the ionic liquid, as well as good mechanical properties based on the polymer, such as flexibility and strechability. These new materials are applicable to flexible or stretchable devices in wearable and flexible electronics applications. Experimental We chose hydrogen bonding copolymers of N,N -dimethylacrylamide (DMAAm) and acrylic acid (AAc) (P(DMAAm- r -AAc)) as the matrix polymers. This copolymer was combined with a hydrophobic ionic liquid, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide ([C 2 mim][NTf 2 ]) to form an ion gel. 3) In order to improve dispersibility of Ga-In in the composite gel, bulk Ga-In was ultra-sonicated in ethanol and the suspension of Ga-In microdroplets was mixed with P(DMAAm- r -AAc) and [C 2 mim][NTf 2 ]. The composite gels were prepared by solution casting method either in the air where thin oxide layer is formed on the Ga-In particles 4) or under inert atmosphere to examine the effects of preparation conditions on their properties. Results and Discussion In tensile tests, Young’s modulus increased with increasing volume fraction of Ga-In in the composite gels. In rheological measurements, storage modulus was higher than loss modulus, confirming soft solid-like behavior of the composite gels. In both measurements, modulus of composite gels was higher than that of ion gels. We found difference in the temperature dependent rheological properties between the composite gels prepared in air and under inert atmosphere. The presence/absence of the surface oxide layer on the Ga-In particles was likely responsible for the difference in the rheological responses. Electronic conductivity was improved by a factor of 10 6 for the composite gels prepared under inert atmosphere compared to that of the composite gels prepared in the air. It was found that the oxide layers on the Ga-In particles had a significant impact on the rheological and electronic properties. However, electronic conductivity of the composite gels prepared under inert atmosphere was still low compared to that of bulk Ga-In. To achieve high electronic conductivity comparable to the bulk value, volume fraction of Ga-In microdroplets needs to be increased in the composite gels. In order to improve dispersibility of high-loading Ga-In in the composite gel, Ga-In microdroplets were prepared with dispersants. The results suggested that there is a trade-off between dispersibility of the Ga-In microdroplets and the electronic conductivity: better dispersibility of Ga-In microdroplets resulted in lower electronic conductivity. Acknowledgement This study was supported in part by Core Research for Evolutionary Science and Technology (CREST) of the Japan Science and Technology Agency (JST). References 1) Kazem, N. et al , Adv. Mater., 2017 , 29, 1-14. 2) Anderson, T. J. et al , Phase Equilibria, 1991 , 12, 64-72. 3) Tamate, R. et al , Adv. Mater , 2018 , 30, 1802792 4) Ren, L. et al , Adv. Funct. Mater., 2016 , 26, 8111-8118. Figure 1

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