Abstract

Inspired by the natural oxygen evolution\nreaction of Photosystem\nII, the earth-abundant and inexpensive manganese oxides (MnO<sub><i>x</i></sub>) have been recognized for their great potential\nas highly efficient and robust materials for water oxidation reaction\n(WORs). To date, most of the heterogeneous, synthesized MnO<sub><i>x</i></sub> catalysts still exhibit lower activities for WORs,\nin comparison to RuO<sub>2</sub> and IrO<sub>2</sub>. Herein, we report\na single-step and scalable synthesis method for mesoporous MnO<sub><i>x</i></sub> materials that is developed through a soft-templated\nmethod. This method allowed precise control of Mn<sup>3+</sup>-rich\nMn<sub>2</sub>O<sub>3</sub> structure as well as pore sizes and crystallinity\nof these mesoporous MnO<sub><i>x</i></sub>. These catalysts\nwere investigated for both photochemical and electrochemical water\noxidation, and they presented a superior activity for water oxidation.\nThe highest turnover frequency of 1.05 × 10<sup>–3</sup> s<sup>–1</sup> was obtained, which is comparable with those\nfor precious metal oxide based catalysts (RuO<sub>2</sub> and IrO<sub>2</sub>). Our results illustrate a guideline to the design and synthesis\nof inexpensive and highly active heterogeneous catalysts for water\noxidation.

Keywords:
Catalysis Mesoporous material Manganese Oxide Manganese oxide Metal Oxygen

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