Measuring the Proton Conductivity of Ion-Exchange Membranes Using Electrochemical Impedance Spectroscopy and Through-Plane Cell

2014 ◽  
Vol 118 (4) ◽  
pp. 1102-1112 ◽  
Author(s):  
Franciélli Müller ◽  
Carlos A. Ferreira ◽  
Denise S. Azambuja ◽  
Carlos Alemán ◽  
Elaine Armelin
2017 ◽  
Vol 541 ◽  
pp. 611-620 ◽  
Author(s):  
Carolina Fernandez-Gonzalez ◽  
John Kavanagh ◽  
Antonio Dominguez-Ramos ◽  
Raquel Ibañez ◽  
Angel Irabien ◽  
...  

2018 ◽  
Vol 11 (04) ◽  
pp. 1850065 ◽  
Author(s):  
Zhirong Xie ◽  
Qingyin Wu ◽  
Fengwei He ◽  
Limei Ai

A novel molybdenum- and vanadium-substituted quaternary heteropoly acid H5SiW9Mo2VO40[Formula: see text][Formula: see text][Formula: see text]13H2O has been synthesized and characterized by IR, UV, TG-DTA and XRD. The proton conductive performance was studied by the electrochemical impedance spectroscopy (EIS), which demonstrated that H5SiW9Mo2VO40[Formula: see text][Formula: see text][Formula: see text]13H2O shows excellent proton conduction performance with proton conductivity reaching [Formula: see text][Formula: see text]S[Formula: see text]cm[Formula: see text] at 60∘C and 80% relative humidity. In the temperature range of measurements, conductivity enhances with higher temperature. The proton conductive mechanism of this new heteropoly acid is the vehicle mechanism due to the activation energy of 31.91[Formula: see text]kJ [Formula: see text] mol[Formula: see text].


Membranes ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 771
Author(s):  
Wenjuan Zhang ◽  
Wei Cheng ◽  
Ramato Ashu Tufa ◽  
Caihong Liu ◽  
David Aili ◽  
...  

Ion-exchange membranes (IEMs) represent a key component in various electrochemical energy conversion and storage systems. In this study, electrochemical impedance spectroscopy (EIS) was used to investigate the effects of structural changes of anion exchange membranes (AEMs) on the bulk membrane and interface properties as a function of solution pH. The variations in the physico/electrochemical properties, including ion exchange capacity, swelling degree, fixed charge density, zeta potentials as well as membrane and interface resistances of two commercial AEMs and cation exchange membranes (CEMs, as a control) were systematically investigated in different pH environments. Structural changes of the membrane surface were analyzed by Fourier transform infrared and X-ray photoelectron spectroscopy. Most notably, at high pH (pH > 10), the membrane (Rm) and the diffusion boundary layer resistances (Rdbl) increased for the two AEMs, whereas the electrical double layer resistance decreased simultaneously. This increase in Rm and Rdbl was mainly attributed to the deprotonation of the tertiary amino groups (-NR2H+) as a membrane functionality. Our results show that the local pH at the membrane-solution interface plays a crucial role on membrane electrochemical properties in IEM transport processes, particularly for AEMs.


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