Fractal diffusion in high temperature polymer electrolyte fuel cell membranes

© 2018 Author(s). The performance of fuel cells depends largely on the proton diffusion in the proton conducting membrane, the core of a fuel cell. High temperature polymer electrolyte fuel cells are based on a polymer membrane swollen with phosphoric acid as the electrolyte, where proton conduction takes place. We studied the proton diffusion in such membranes with neutron scattering techniques which are especially sensitive to the proton contribution. Time of flight spectroscopy and backscattering spectroscopy have been combined to cover a broad dynamic range. In order to selectively observe the diffusion of protons potentially contributing to the ion conductivity, two samples were prepared, where in one of the samples the phosphoric acid was used with hydrogen replaced by deuterium. The scattering data from the two samples were subtracted in a suitable way after measurement. Thereby subdiffusive behavior of the proton diffusion has been observed and interpreted in terms of a model of fractal diffusion. For this purpose, a scattering function for fractal diffusion has been developed. The fractal diffusion dimension dw and the Hausdorff dimension df have been determined on the length scales covered in the neutron scattering experiments

Hydrogen diffusivity and electrolyte permeability of the Zirfon PERL separator for alkaline water elctrolysis

The hydrogen and oxygen evolved during alkaline water electrolysis with liquid KOH electrolytes are typically separated using porous separators such as Zirfon PERL (Agfa), a commercially available composite of zirconium oxide and polysulfone. In this study, the hydrogen diffusivity (driven by concentration differences) and electrolyte permeability (driven by differential pressures) of the Zirfon PERL separator were characterized as a function of the temperature and molarity of the KOH filling. The diffusivity of hydrogen in the separator was found to be approximately 16% of that of the electrolyte filling inside its pores. With respect to water electrolysis conditions, the extent of hydrogen cross-permeation caused by the convection of the cross-permeating electrolyte was estimated and compared to that caused by diffusion. On the basis of the physically characterized mechanisms, smaller pores were predicted to reduce the differential pressure driven gas cross-permeation