High performance polyvinyl alcohol/calcium titanate nanocomposite anion-exchange membranes as separators in redox flow batteries

Low ionic conductivity and poor chemical stability are the two key parameters that limit the use of many anion-exchange membranes in electrochemical applications like rechargeable batteries and fuel cells. Herein we report a method for the synthesis of a high performance anion-exchange membrane fabr...

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Veröffentlicht in:Polymer bulletin (Berlin, Germany) Germany), 2018-10, Vol.75 (10), p.4409-4428
Hauptverfasser: Moly, P. P., Jeena, C. B., Elsa, P. J., Ambily, K. J., Joy, V. T.
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Sprache:eng
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Zusammenfassung:Low ionic conductivity and poor chemical stability are the two key parameters that limit the use of many anion-exchange membranes in electrochemical applications like rechargeable batteries and fuel cells. Herein we report a method for the synthesis of a high performance anion-exchange membrane fabricated by incorporating calcium titanate nanoparticles (CaTiO 3 ) into polyvinyl alcohol (PVA) matrix. The CaTiO 3 was synthesized by a new co-precipitation method from a solution of two simple precursors, viz potassium titanyl oxalate and calcium chloride. The XRD data of the synthesized nanoparticles indicate a phase pure orthorhombic perovskite structure. Morphological features investigated with SEM and TEM studies, reveal that the CaTiO 3 is having spherical shape with a diameter of approximately 200 nm. The PVA/CaTiO 3 nanocomposite membranes were fabricated by solution casting method from a well dispersed suspension of CaTiO 3 in PVA and characterized by FT-IR spectroscopy, TGA, SEM, AC impedance analysis and tensile strength measurements. The membranes with 30 wt% CaTiO 3 content possess ionic conductivity of 66 mS cm −1 at room temperature. The electrochemical performance of an all-iron redox flow cell was studied using galvanostatic charge–discharge tests using the above nanocomposite membrane as separator and the system exhibited a coulombic efficiency of 75% during the charge–discharge cycles.
ISSN:0170-0839
1436-2449
DOI:10.1007/s00289-018-2277-2