4.8 Article

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

Journal

SCIENCE
Volume 353, Issue 6303, Pages 1011-1014

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aaf5050

Keywords

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Funding

  1. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences [DE-SC0008685]
  2. SUNCAT Center for Interface Science and Catalysis
  3. Center on Nanostructuring for Efficient Energy Conversion at Stanford University, an Energy Frontier Research Center - DOE, Office of Science [DE-SC0001060]
  4. DARE (Diversifying Academia, Recruiting Excellence) Doctoral Fellowship - Vice Provost for Graduate Education at Stanford University
  5. DOE, Office of Science, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-AC02-76SF00515]
  6. Global Climate and Energy Project at Stanford University
  7. NSF [DGE-114747]
  8. Morgridge Family Stanford Graduate Fellowship

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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. 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 rutheniumoxide (RuOx) systems, the only other OER catalysts that have reasonable activity in acidic electrolyte.

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