Nature Communications (Aug 2025)

Tunnel-structured IrOx unlocks catalytic efficiency in proton exchange membrane water electrolyzers

  • Mingcheng Zhang,
  • Wei An,
  • Qianqian Liu,
  • Yuzhu Jiang,
  • Xiao Zhao,
  • Hui Chen,
  • Yongcun Zou,
  • Xiao Liang,
  • Xiaoxin Zou

DOI
https://doi.org/10.1038/s41467-025-62861-0
Journal volume & issue
Vol. 16, no. 1
pp. 1 – 15

Abstract

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Abstract Proton exchange membrane water electrolyzers face challenges due to high iridium loading and sluggish oxygen evolution reaction kinetics when using conventional rutile-structured iridium oxide nanocatalysts. Here we find that iridium oxide catalysts with a specific tunnel-type crystal structure exhibit highly localized reactivity, where regions at tunnel mouths drive oxygen evolution far more efficiently than tunnel-wall regions. The intrinsic activity of tunnel mouths is 25-fold higher than that of tunnel walls, with shorter nanorods achieving a better balance between active site exposure and electron/mass transport efficiency. When implemented in proton exchange membrane water electrolyzers, this engineered catalyst achieves notable performance at low iridium loading (0.28 mgIr cm−2), delivering over 2.0 A cm−2 at 1.8 V (80 °C) and operating stably for 1800 h—notably outperforming conventional catalysts. Our work identifies catalytic hotspots in tunnel-structured oxides and demonstrates their rational integration into high-performance, durable electrolyzer systems.