Understanding degradation mechanisms in SrIrO oxygen evolution electrocatalysts. Chemical and structural microscopy at the nanoscale
Creators
- Ben‐Naim, Micha1, 2
- Burke Stevens, Michaela1, 2
- Jaramillo, Thomas F.1, 2
- Liu, Yunzhi3
- Wette, Melissa R.3
- Clemens, Bruce M.3
- Sinclair, Robert3
- Lee, Kyuho4, 5
- Boubnov, Alexey6
- Davis, Ryan C.6
- Bare, Simon R.6
- Trofimov, Artem A.7
- Ievlev, Anton V.8
- Belianinov, Alex8
- Hikita, Yasuyuki5
- Hwang, Harold Y.9, 5
- Higgins, Drew C.10, 1, 2
- 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 SrIrO 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 SrIrO 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 IrO-rich surface to dissolve and be regenerated by Sr leaching. The characterization approaches utilized herein and mechanistic insights into SrIrO 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.202101542Additional 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
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 53065299
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ELECTROCATALYSTS; ION MICROPROBE ANALYSIS; ION MICROSCOPY; IRIDIUM OXIDES; MASS SPECTROSCOPY; OXYGEN; STRONTIUM OXIDES; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; CATALYSTS; CHALCOGENIDES; CHEMICAL ANALYSIS; ELECTRON MICROSCOPY; ELEMENTS; IRIDIUM COMPOUNDS; MICROANALYSIS; MICROSCOPY; NONDESTRUCTIVE ANALYSIS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; REFRACTORY METAL COMPOUNDS; SPECTROSCOPY; STRONTIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Notes
- AID: 2101542