Published August 2021 | Version v1
Journal article

Understanding degradation mechanisms in SrIrO3 oxygen evolution electrocatalysts. Chemical and structural microscopy at the nanoscale

  • 1. SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, Menlo Park, CA, 94205 (United States)
  • 2. Department of Chemical Engineering, Stanford University, Stanford, CA, 94305 (United States)
  • 3. Department of Materials Science and Engineering, Stanford University, Stanford, CA, 94305 (United States)
  • 4. Department of Physics, Stanford University, Stanford, CA, 94305 (United States)
  • 5. Stanford Institute for Materials and Energy Sciences, SLAC National Accelerator Laboratory, Menlo Park, CA, 94205 (United States)
  • 6. Stanford Synchrotron Radiation Light Source, SLAC National Accelerator Laboratory, Menlo Park, CA, 94025 (United States)
  • 7. Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831 (United States)
  • 8. Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831 (United States)
  • 9. Department of Applied Physics, Stanford University, Stanford, CA, 94305 (United States)
  • 10. Department of Chemical Engineering, McMaster University, Hamilton, Ontario, L8S 4L8 (Canada)

Description

Designing acid-stable oxygen evolution reaction electrocatalysts is key to developing sustainable energy technologies such as polymer electrolyte membrane electrolyzers but has proven challenging due to the high applied anodic potentials and corrosive electrolyte. This work showcases advanced nanoscale microscopy techniques supported by complementary structural and chemical characterization to develop a fundamental understanding of stability in promising SrIrO3 thin film electrocatalyst materials. Cross-sectional high-resolution transmission electron microscopy illustrates atomic-scale bulk and surface structure, while secondary ion mass spectrometry imaging using a helium ion microscope provides the nanoscale lateral elemental distribution at the surface. After accelerated degradation tests under anodic potential, the SrIrO3 film thins and roughens, but the lateral distribution of Sr and Ir remains homogeneous. A layer-wise dissolution mechanism is hypothesized, wherein anodic potential causes the IrOx-rich surface to dissolve and be regenerated by Sr leaching. The characterization approaches utilized herein and mechanistic insights into SrIrO3 are translatable to a wide range of catalyst systems. (© 2021 Wiley‐VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/adfm.202101542

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Functional Materials (Internet)
Journal Volume
31
Journal Issue
34
Journal Page Range
p. 1-11
ISSN
1616-3028

Optional Information

Notes
AID: 2101542