Published 2016 | Version v1
Journal article

A highly active and stable IrOx/SrIrO3 catalyst for the oxygen evolution reaction

  • 1. Stanford University, Stanford, CA (United States)
  • 2. SLAC National Accelerator Laboratory, Menlo Park, CA (United States)

Description

Oxygen electrochemistry plays a key role in renewable energy technologies such as fuel cells and electrolyzers, but the slow kinetics of the oxygen evolution reaction (OER) limit the performance and commercialization of such devices. Here we report an iridium oxide/strontium iridium oxide (IrOx/SrIrO3) catalyst formed during electrochemical testing by strontium leaching from surface layers of thin films of SrIrO3. This catalyst has demonstrated specific activity at 10 milliamps per square centimeter of oxide catalyst (OER current normalized to catalyst surface area), with only 270 to 290 millivolts of overpotential for 30 hours of continuous testing in acidic electrolyte. Here, density functional theory calculations suggest the formation of highly active surface layers during strontium leaching with IrO3 or anatase IrO2 motifs. The IrOx/SrIrO3 catalyst outperforms known IrOx and ruthenium oxide (RuOx) systems, the only other OER catalysts that have reasonable activity in acidic electrolyte.

Availability note (English)

Available from http://www.osti.gov/pages/biblio/1349300; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period

Additional details

Publishing Information

Journal Title
Science (Washington, D.C.)
Journal Volume
353
Journal Issue
6303
Journal Page Range
p. 1011-1014
ISSN
0036-8075

Optional Information

Contract/Grant/Project number
AC02-76SF00515
Funding organization
USDOE Office of Science - SC, Basic Energy Sciences (BES) (SC-22) (United States)
Secondary number(s)
OSTIID--1349300