Cost reduction and
fast scale-up of electrolyzer technologies are
essential for decarbonizing several crucial branches of industry.
For polymer electrolyte water electrolysis, this requires a dramatic
reduction of the expensive and scarce iridium-based catalyst, making
its efficient utilization a key factor. The interfacial properties
between the porous transport layer (PTL) and the catalyst layer (CL)
are crucial for optimal catalyst utilization. Therefore, it is essential
to understand the relationship between this interface and electrochemical
performance. In this study, we fabricated a matrix of two-dimensional
interface layers with a well-known model structure, integrating them
as an additional layer between the PTL and the CL. By characterizing
the performance and conducting an in-depth analysis of the overpotentials,
we were able to estimate the catalyst utilization at different current
densities, correlating them to the geometric properties of the model
PTLs. We found that large areas of the CL become inactive at increasing
current density either due to dry-out, oxygen saturation (under the
PTL), or the high resistance of the CL away from the pore edges. We
experimentally estimated the water penetration in the CL under the
PTL to be ≈20 μm. Experimental results were corroborated
using a 3D-multiphysics model to calculate the current distribution
in the CL and estimate the impact of membrane dry-out. Finally, we
observed a strong pressure dependency on performance and high-frequency
resistance, which indicates that with the employed model PTLs, a significant
gas phase accumulates in the CL under the lands, hindering the distribution
of liquid water. The findings of this work can be extrapolated to
improve and engineer PTLs with advanced interface properties, helping
to reach the required target goals in cost and iridium loadings.