Abstract
Anion exchange membrane water electrolysis (AEMWE) is a promising technology to produce hydrogen from low-cost, renewable power sources. Recently, the efficiency and durability of AEMWE have improved significantly due to advances in the anion exchange polymers and catalysts. To achieve performances and lifetimes competitive with proton exchange membrane or liquid alkaline electrolyzers, however, improvements in the integration of materials into the membrane electrode assembly (MEA) are needed. In particular, the integration of the oxygen evolution reaction (OER) catalyst, ionomer, and transport layer in the anode catalyst layer has significant impacts on catalyst utilization and voltage losses due to the transport of gases, hydroxide ions, and electrons within the anode. This study investigates the effects of the properties of the OER catalyst and the catalyst layer morphology on performance. Using cross-sectional electron microscopy and in-plane conductivity measurements for four PGM-free catalysts, we determine the catalyst layer thickness, uniformity, and electronic conductivity and further use a transmission line model to relate these properties to the catalyst layer resistance and utilization. We find that increased loading is beneficial for catalysts with high electronic conductivity and uniform catalyst layers, resulting in up to 55% increase in current density at 2 V due to decreased kinetic and catalyst layer resistance losses, while for catalysts with lower conductivity and/or less uniform catalyst layers, there is minimal impact. This work provides important insights into the role of catalyst layer properties beyond intrinsic catalyst activity in AEMWE performance.
| Original language | English |
|---|---|
| Pages (from-to) | 10806-10819 |
| Number of pages | 14 |
| Journal | ACS Catalysis |
| Volume | 14 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 19 2024 |
Funding
We acknowledge financial support from the US DOE Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office, under the ElectroCat Consortium, DOE technology managers McKenzie Hubert and William Gibbons, and DOE program managers David Peterson and Dimitrios Papageorgopolous. This work was authored by the National Renewable Energy Laboratory, operated by Alliance for Sustainable Energy, LLC, for the U.S. Department of Energy (DOE) under Contract No. DE-AC36-08GO28308. This work was authored in part by Los Alamos National Laboratory operated by Triad National Security, LLC, under US DOE contract no. 89233218CNA000001 and by Oak Ridge National Laboratory operated by UT-Battelle, LLC, under contract no. DE-AC05-00OR22725. STEM research was conducted as part of a user project at the Center for Nanophase Materials Sciences (CNMS), which is a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. D.H.M., R.T.H., and T.F.J. acknowledge support from the Stanford Doerr School of Sustainability Accelerator for XPS studies. D.H.M. acknowledges support from a TomKat Center for Sustainable Energy fellowship for Translational Research. Part of this work was performed at the Stanford Nano Shared Facilities (SNSF), supported by the National Science Foundation under award ECCS-2026822. The views expressed in the article do not necessarily represent the views of the DOE or the U.S. Government. The U.S. Government retains, and the publisher, by accepting the article for publication, acknowledges that the U.S. Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this work or to allow others to do so for U.S. Government purposes.
Keywords
- anion exchange membrane
- catalyst layer
- electrocatalysis
- oxygen evolution reaction
- water electrolysis