Toward an Active and Stable Catalyst for Oxygen Evolution in Acidic Media: Ti‐Stabilized MnO2 |
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Authors: | Rasmus Frydendal Elisa A Paoli Ib Chorkendorff Jan Rossmeisl Ifan E L Stephens |
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Institution: | 1. Center for Individual Nanoparticle Functionality, Department of Physics, Building 312, Technical University of Denmark, Kgs. Lyngby, Denmark;2. Center for Atomic‐scale Materials Design, Department of Physics, Building 307, Technical University of Denmark, Kgs. Lyngby, Denmark;3. Department of Chemistry, University of Copenhagen, K?benhavn ?, Denmark |
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Abstract: | Catalysts are required for the oxygen evolution reaction, which are abundant, active, and stable in acid. MnO2 is a promising candidate material for this purpose. However, it dissolves at high overpotentials. Using first‐principles calculations, a strategy to mitigate this problem by decorating undercoordinated surface sites of MnO2 with a stable oxide is developed here. TiO2 stands out as the most promising of the different oxides in the simulations. This prediction is experimentally verified by testing sputter‐deposited thin films of MnO2 and Ti–MnO2. A combination of electrochemical measurements, quartz crystal microbalance, inductively coupled plasma mass spectrometry measurements, and X‐ray photoelectron spectroscopy is performed. Small amounts of TiO2 incorporated into MnO2 lead to a moderate improvement in stability, with only a small decrease in activity. This study opens up the possibility of engineering surface properties of catalysts so that active and abundant nonprecious metal oxides can be used in acid electrolytes. |
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Keywords: | catalysis corrosion density functional theory electrochemistry oxygen evolution |
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