4.8 Article

Mechanistic Investigation of Water Oxidation Catalyzed by Uniform, Assembled MnO Nanoparticles

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 6, 页码 2277-2285

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b10657

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资金

  1. Global Frontier R&D Program of the Center for Multiscale Energy System - National Research Foundation under the Ministry of Science, ICT future, Korea [2011-0031571]
  2. KIST Institutional Program [0543-20160004]
  3. Ministry of Trade, Industry & Energy (MOTIE) under Industrial Strategic Technology Development Program, Korea [0417-2016-0019]
  4. Research Institute of Advanced Materials (RIAM) at Seoul National University
  5. C1 Gas Refinery Program through the NRF - Ministry of Science, ICT & Future Planning [2015M3D3A1A01064876]
  6. JSPS [26288092]
  7. [15J10583]
  8. National Research Foundation of Korea [2015M3D3A1A01064876] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  9. Grants-in-Aid for Scientific Research [26288092, 15J10583] Funding Source: KAKEN

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The development of active water oxidation catalysts is critical to achieve high efficiency in overall water splitting. Recently, sub 10 nm-sized monodispersed partially oxidized manganese oxide nanoparticles were shown to exhibit not only superior catalytic performance for oxygen evolution, but also unique electrokinetics, as compared to their bulk counterparts. In the present work, the water oxidizing mechanism of partially oxidized MnO nanoparticles was investigated using integrated in situ spectroscopic and electrokinetic analyses. We successfully demonstrated that, in contrast to previously reported manganese (Mn)-based catalysts, Mn(III) species are stably generated on the, surface of MnO nanoparticles via a proton-coupled electron transfer pathway. Furthermore, we confirmed as to MnO nanoparticles that the one-electron oxidation step from Mn(II) to Mn(III) is no longer the rate-determining step for water oxidation and that Mn(W)=O species are generated as reaction intermediates during catalysis.

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