The ion and water transport properties of K+ and Na+ form perfluorosulfonic acid polymer. (20th August 2018)

• Record Type: Journal Article
• Authors: Peng, Jing; Tian, Mengkun; Cantillo, Nelly M.; Zawodzinski, Thomas
• Is Part Of: Electrochimica acta. Volume 282(2018)
• Page Start: 544
• Page End: 554
• Publication Date: 2018-08-20
• Subjects: Cation exchange membrane -- Partitioning -- Conductivity -- Ionic mobility -- Cluster; Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2018.06.035
• Languages: English
• ISSNs: 0013-4686

Abstract

Abstract: In this work, we explore the behavior of membranes under conditions that are relevant to ion-exchange membranes used in a variety of electrochemical engineering applications, extending beyond the heavily-studied fuel cell application and previous studies of fully hydrated systems. We report the water uptake, density and conductivity of membranes determined at various hydration states of K +, Na + and K + /Na + mixed form perfluorosulfonate membranes. Water uptake decreases with increasing K + content in the membrane, consistent with increasing average cation size and decreasing hydration energy. However, for membranes at the same water content, the conductivity increased with increasing K + fraction, in spite of the fact that the size of K + is larger than that of Na + . Analysis of data on the basis of percentage conducting volume reveals that the membranes with higher K + content show a much higher conductivity (with higher cation mobility) at percentage conducting volumes higher than 10%. One reason for this behavior may be due to a higher extent of dissociation for K + from the fixed anion site. TEM results show a larger cluster size in K + form membranes, another possible reason for faster K + transport. Pulsed field gradient (PFG) Nuclear Magnetic Resonance (NMR) shows that water diffusion coefficient in the membranes with higher K + fraction is higher than for samples with lower K + fraction. FT-IR bands shift with the change of cation content, supporting the suggestion of a higher degree of cation-sulfonate dissociation and weaker hydrogen bonding interactions between cation and water molecules for membranes with higher K + content.