IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm−2 in acidic media

  • Rui Li
  • , Haiyun Wang
  • , Fei Hu
  • , K. C. Chan
  • , Xiongjun Liu
  • , Zhaoping Lu
  • , Jing Wang
  • , Zhibin Li
  • , Longjiao Zeng
  • , Yuanyuan Li
  • , Xiaojun Wu
  • , Yujie Xiong

Research output: Journal article publicationJournal articleAcademic researchpeer-review

177 Citations (Scopus)

Abstract

A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm−2 at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm−2 at least 800 h with a negligible degradation rate of ~4 μV h−1. Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO2)n clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO2 clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers.

Original languageEnglish
Article number3540
JournalNature Communications
Volume12
Issue number1
DOIs
Publication statusPublished - Dec 2021

ASJC Scopus subject areas

  • General Chemistry
  • General Biochemistry,Genetics and Molecular Biology
  • General Physics and Astronomy

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