We present an investigation of the structure and rheological behavior of catalyst inks for low-temperature polymer electrolyte membrane water electrolyzers (PEMWE). The ink consists of iridium oxide (IrO2) catalyst particles… Click to show full abstract
We present an investigation of the structure and rheological behavior of catalyst inks for low-temperature polymer electrolyte membrane water electrolyzers (PEMWE). The ink consists of iridium oxide (IrO2) catalyst particles and Nafion ionomer dispersed in a mixture of 1-propanol and water. The effects of ionomer concentration and catalyst concentration on the microstructure of catalyst ink were studied. Studies on dilute inks (0.1 wt% IrO2) using zeta potential and dynamic light scattering (DLS) measurements indicated a strong adsorption of ionomer onto the catalyst particles which resulted in an increase in the ΞΆ-potential and the z-average diameter. Steady-shear and dynamic-oscillatory-shear rheological measurements of concentrated IrO2 dispersions (35 wt% IrO2) indicated that the particles are strongly agglomerated in the absence of ionomer. The addition of even a small amount of ionomer (2.4 wt% with respect to total solids) caused the rheology to transition from shear thinning to Newtonian due to significantly reduced agglomerated structure due to stabilization of the aggregates by the ionomer, consistent with the behavior of dilute inks. At intermediate ionomer loadings, between 2.4 wt% to 9 wt%, the viscosity increased with increasing ionomer wt%, though remained Newtonian, predominantly due to increasing ionomer volume fraction in the ink. For ionomer loadings greater than 9 wt%, the particles were found to be flocculated, likely induced by dispersed ionomer. The flocculated inks exhibited strong shear-thinning and gel-like behaviors in steady-shear and oscillatory shear rheology. The onset of flocculation was found to be sensitive to the catalyst concentration, where below 35 wt% of IrO2, flocculation was not observed. The rheological observations were further verified by ultra-small-angle X-ray scattering (USAXS).
               
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