Conductivity study of Zeolitic Imidazolate Frameworks, Tetrabutylammonium hydroxide doped with Zeolitic Imidazolate Frameworks, and mixed matrix membranes of Polyetherimide/Tetrabutylammonium hydroxide doped with Zeolitic Imidazolate Frameworks for proton conducting applications

沸石咪唑盐骨架 咪唑酯 聚醚酰亚胺 兴奋剂 氢氧化物 金属有机骨架 电导率 材料科学 电解质 无机化学 分析化学(期刊) 化学工程 化学 吸附 聚合物 物理化学 色谱法 复合材料 电极 工程类 生物化学 光电子学
作者
J. Vega,Andreu Andrio,A.A. Lemus,L. F. del Castillo,Vicente Compañ
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:258: 153-166 被引量:34
标识
DOI:10.1016/j.electacta.2017.10.095
摘要

ZIF-8 (Z8), ZIF-67 (Z67), and ZMix, a Zn/Co bimetallic zeolitic imidazolate framework (ZIF), were synthesized and doped with tetrabutylammonium hydroxide (ZIFsT). The obtained powders were used as fillers for polyetherimide (PEI) at a concentration of 20 wt %. The presence of the three ZIFsT in the polymeric matrix enhanced proton transport relative to that observed for PEI or ZIFs alone. The real and imaginary parts of the complex conductivity were obtained for each of the six materials, and the temperature and frequency dependence of the real part was analyzed. The results at different temperatures show that the dc-conductivity are about three orders of magnitude higher for the doped ZIFsT materials than for the PEI/ZIFsT membranes. In addition, the conductivity of the PEI/ZIFsT membranes increases five or six times when the temperature is changed from 25 °C to 55 °C. For these materials, the conductivity measurements have a linear dependency with frequency, which allowed for the creation of a master curve. It was also found that the PEI/ZMixT membrane activation energy is four times smaller than that of PEI/Z8T membranes and five times smaller than that of PEI/Z67T. Similarly, the real and imaginary parts of the complex dielectric constant were obtained, and the tan δ was evaluated. Using this value, the diffusion coefficient and the charge carrier density were obtained. A discussion of the proton transport mechanism through the membrane is given, and a comparison of this work with those on similar electrolyte membranes is included.
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