Abstract
Proton exchange membrane water electrolyzers rely on relatively expensive Ir-based catalysts for efficient and durable hydrogen production. To reduce system costs, Ir loadings can be reduced if performance and durability are maintained. Sputter deposition is a readily scalable method to synthesize uniform, low-loading catalyst layers with controlled composition. A catalyst applied directly to the porous transport layer can have advantages for performance, manufacturing simplicity, and catalyst recovery. Suitable porous transport layer porosity can minimize activity losses when reducing loadings. Here, methods are presented to deposit metallic Ir as well as amorphous and rutile Ir oxides. The activity and durability of these materials in the porous transport electrode architecture is evaluated. The metallic and amorphous forms have better initial activity, however, operation at 3 A cm−2 with 0.1 mg Ir cm−2 shows that only rutile IrO2 maintains performance beyond 100 h with a 50 mV improvement after 700 h. A >10x reduced dissolution rate is shown for rutile IrO2. With a low-porosity transport layer and 0.4 mg Ir cm−2, a steady-state voltage decay rate of 6 µV h−1 is achieved. The results demonstrate that sputter-deposited rutile IrO2 porous transport electrodes with low Ir loading can be operated at high current density to reduce hydrogen production costs.
| Original language | English |
|---|---|
| Journal | Advanced Science |
| DOIs | |
| State | Accepted/In press - 2026 |
Funding
This work was authored, in part, by the National Renewable Energy Laboratory for the U.S. Department of Energy (DOE) under Contract No. DE‐AC36‐08GO28308. Funding provided by the U.S. Department of Energy Office of Energy Efficiency and Renewable Energy Hydrogen and Fuel Cells Technologies Office. Electron microscopy research was supported by the Center for Nanophase Materials Sciences (CNMS), which is a U.S. Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. The Tescan SEM instrument at the Colorado School of Mines was supported by the National Science Foundation under grant No.DMR‐1828454. 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 allow others to do so, for U.S. Government purposes.
Keywords
- electrolysis
- iridium oxide
- oxygen evolution
- porous transport electrode
- rutile
- sputter deposition