Low-iridium stabilized ruthenium oxide anode catalyst for durable proton-exchange membrane water electrolysis

  • Chang Qiu
  • , Chase Sellers
  • , Zhen Yu Wu
  • , David A. Cullen
  • , Eli Stavitski
  • , Akhil Tayal
  • , Tae Ung Wi
  • , Mounika Kodali
  • , Bryan Erb
  • , Andrew Smeltz
  • , Feng Yang Chen
  • , Yuge Feng
  • , Zhou Yu
  • , Ahmad Elgazzar
  • , Tanguy Terlier
  • , Thomas P. Senftle
  • , Haotian Wang

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

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 languageEnglish
JournalNature Nanotechnology
DOIs
StateAccepted/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.

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