Abstract
While mixing iridium (Ir) with ruthenium oxide (RuO2) has proven to be an effective strategy for reducing Ir loading in anode catalysts for proton-exchange membrane (PEM) water electrolysers, achieving industrially relevant long-term stability typically requires an Ir-rich, Ru-lean combination. Here, by combining density functional theory with Metropolis Monte Carlo methods, we discovered that sufficient stabilization in the RuO2 lattice could be achieved with less than 50 at.% of Ir, and that Ir in the first subsurface layer plays a critical role. By effectively dispersing Ir dopants within the RuO2 lattice, we demonstrated an Ir:Ru atomic ratio of only 1:6 that exhibited exceptional stability for over 1,500 h of continuous water electrolysis at 2 A cm−2. Our Ru6IrOx catalyst has the potential to reduce Ir loading by 80% compared with current commercial PEM water electrolysers, and its stability was further validated under industrial testing conditions in a 25-cm2 PEM electrolyser.
| Original language | English |
|---|---|
| Journal | Nature Nanotechnology |
| DOIs | |
| State | Accepted/In press - 2025 |
Funding
This work was supported by the Robert A. Welch Foundation (grant no. C-2051-20230405), the the David and Lucile Packard Foundation (grant 2020-71371) and National Science Foundation (grant no. 2143941). Electron microscopy research was supported by the Center for Nanophase Materials Sciences (CNMS), which is a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. This research used the Inner Shell Spectroscopy (ISS, 8-ID) of the National Synchrotron Light Source II, a US Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under contract no. DE-SC0012704. We acknowledge the use of the Shared Equipment Authority and Electron Microscopy Center at Rice University for their contributions to this research.