From operando investigations to implementation of Ni-MOF-74 oxygen evolution electrocatalysts
Creators
- 1. Paul Scherrer Institute (PSI) Center for Energy and Environmental Sciences, Villigen, Aargau, Switzerland
- 2. Paul Scherrer Institute (PSI) Center for Photon Science, Villigen, Aargau, Switzerland
- 3. Department of Energy Conversion and Storage, Technical University of Denmark, Kongens Lyngby, Denmark
- 4. Eidgenössische Technische Hochschule Zürich (ETHZ), Institute of Molecular Physical Science, Zürich, Switzerland
* Contact person
Description
Metal-organic frameworks (MOFs) as electrocatalysts for the alkaline oxygen evolution reaction (OER) show promising catalytic activity by offering great variability and high surface areas, enabling performance optimization and mechanistic studies. However, their stability during reaction and the structure-performance relationship defining the origin of the high OER activity, are still vigorously debated. Herein, we leverage operando X-ray absorption spectroscopy and operando X-ray diffraction to unveil the structural and electronic transformations of Ni-MOF-74 during OER. We identify the irreversible destruction of the MOF-74 crystal into a highly OER active, amorphous NiOOH-metal organic compound. Based on these findings, we propose an amorphous Ni metal organic compound (Ni-MOC*) for achieving high current densities both in a three-electrode cell (14 A gNi-1 at 1.5 VRHE) and in an anion exchange membrane water electrolyzer (AEM-WE) with a stable AEM-WE performance exceeding 100 h at 500 mA cm-2.
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References
Journal reference J. Linke, T. Rohrbach, A. H. Clark, M. Andrzejewski, N. P. M. Casati, F. L. Buchauer, M. R. Kraglund, C. Chatzichristodoulou, E. Meade, M. Ranocchiari, T. J. Schmidt, E. Fabbri, Advanced Energy Materials (submitted).