Electrically conductive porous Ti3C2T x MXene-polymer composites from high internal phase emulsions (HIPEs)

材料科学 聚合物 复合材料 多孔性 聚合 X射线光电子能谱 扫描电子显微镜 相(物质) 渗透(认知心理学) 化学工程 电导率 有机化学 物理化学 神经科学 化学 工程类 生物
作者
Huaixuan Cao,Yifei Wang,Anubhav Sarmah,Kaiwei Liu,Zeyi Tan,Kailash Arole,Jodie L. Lutkenhaus,Miladin Radović,Micah J. Green,Emily Pentzer
出处
期刊:2D materials [IOP Publishing]
卷期号:9 (4): 044004-044004 被引量:12
标识
DOI:10.1088/2053-1583/ac914c
摘要

Abstract Porous MXene-polymer composites have gained attention due to their low density, large surface area, and high electrical conductivity, which can be used in applications such as electromagnetic interference shielding, sensing, energy storage, and catalysis. High internal phase emulsions (HIPEs) can be used to template the synthesis of porous polymer structures, and when solid particles are used as the interfacial agent, composites with pores lined with the particles can be realized. Here, we report a simple and scalable method to prepare conductive porous MXene/polyacrylamide structures via polymerization of the continuous phase in oil/water HIPEs. The HIPEs are stabilized by salt flocculated Ti 3 C 2 T x nanosheets, without the use of a co-surfactant. After polymerization, the polyHIPE structure consists of porous polymer struts and pores lined with Ti 3 C 2 T x nanosheets, as confirmed by scanning electron microscopy, energy dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The pore size can be tuned by varying the Ti 3 C 2 T x concentration, and the interconnected Ti 3 C 2 T x network allows for electrical percolation at low Ti 3 C 2 T x loading; further, the electrical conductivity is stable for months indicating that in these composites, the nanosheets are stable to oxidation at ambient conditions. The polyHIPEs also exhibit rapid radio frequency heating at low power (10 °C s −1 at 1 W). This work demonstrates a simple approach to accessing electrically conductive porous MXene/polymer composites with tunable pore morphology and good oxidation stability of the nanosheets.
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