| Literature DB >> 30869187 |
Ailong Li1,2,3, Hideshi Ooka2, Nadège Bonnet2, Toru Hayashi2,4, Yimeng Sun1,3, Qike Jiang1, Can Li1, Hongxian Han1,5, Ryuhei Nakamura2,6.
Abstract
Efficient, earth-abundant, and acid-stable catalysts for the oxygen evolution reaction (OER) are missing pieces for the production of hydrogen via water electrolysis. Here, we report how the limitations on the stability of 3d-metal materials can be overcome by the spectroscopic identification of stable potential windows in which the OER can be catalyzed efficiently while simultaneously suppressing deactivation pathways. We demonstrate the benefits of this approach using gamma manganese oxide (γ-MnO2 ), which shows no signs of deactivation even after 8000 h of electrolysis at a pH of 2. This stability is vastly superior to existing acid-stable 3d-metal OER catalysts, but cannot be realized if there is a deviation as small as 50-mV from the stable potential window. A stable voltage efficiency of over 70 % in a polymer-electrolyte membrane (PEM) electrolyzer further verifies the availability of this approach and showcases how materials previously perceived to be unstable may have potential application for water electrolysis in an acidic environment.Entities:
Keywords: acidic conditions; manganese oxide; proton-exchange membrane electrolyzer; stable potential windows; water oxidation
Year: 2019 PMID: 30869187 DOI: 10.1002/anie.201813361
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336