Mass transport losses (η mt x ) play a significant role at high current densities in polymer electrolyte water electrolyzers (PEWEs). Previous work has shown that η mt x depends on the porous transport layer (PTL) structure, although a clear correlation between the material morphology and η mt x has not been established. In this work, we experimentally determine the overpotential η H + C La associated with the proton transport in the anodic catalyst layer by measuring the ionic resistance in the catalyst layer using electrochemical impedance spectroscopy (EIS) and the transmission-line model. We found that overpotentials, including η H + C La , depend on the PTL morphologic surface properties.