Chung-Hao Kuo (1290198)IslamM. Mosa (1443739)Altug S. Poyraz (1642678)Sourav Biswas (1574509)Abdelhamid M. El-Sawy (1601320)Wenqiao Song (1525879)Zhu Luo (1525882)Sheng-Yu Chen (1497346)JamesF. Rusling (1642681)Jie He (132999)Steven L. Suib (1290195)
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.
Chung‐Hao KuoIslam M. MosaAltuğ S. PoyrazSourav BiswasAbdelhamid M. El‐SawyWenqiao SongZhu LuoSheng-Yu ChenJames F. RuslingJie HeSteven L. Suib
Prashanth W. MenezesArindam IndraOphir LevyKamalakannan KailasamVitaly GutkinJohannes PfrommerMatthias Drieß
Mostafa Malek‐mohammadiAkram Heydari‐turkmaniSaeed ZakaviNasser Nikfarjam