4.7 Article

Heptanuclear Co5IICo2III Cluster as Efficient Water Oxidation Catalyst

期刊

INORGANIC CHEMISTRY
卷 56, 期 3, 页码 1591-1598

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b02698

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资金

  1. NSFC [21571115, 21201110]
  2. Natural Science Foundation of Shandong Province [ZR2014BM027]
  3. Young Scholars Program of Shandong University [2015WLJH24]
  4. Fundamental Research Funds of Shandong University [104.205.2.5]

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Inspired by the transition-metal-oxo cubical Mn4CaO5 in photosystem II, we herein report a disc-like heptanudear mixed-valent cobalt cluster, [(Co5Co2III)-Co-II(mdea)(4)(N-3)(2)(CH3CN)(6)(OH)(2)(H2O)(2)center dot 4ClO(4)] (1, H(2)Mdea = N-methyldiethanolamine), for photocatalytic oxygen evolution. The topology of the Co-7 core resembles a small piece of cobaltate protected by terminal H2O, N-3(-), CH3CN, and multidentate N-methyldiethanolamine at the periphery. Under the optimal photocatalytic conditions, 1 exhibits water oxidation activity with a turnover number (TON) of 210 and a turnover frequency (TOFinital) of 0.23 s(-1). Importantly, electrospray mass spectrometry (ESI-MS) was used to not only identify the possible main active species in the water oxidation reaction but also monitor the evolutions of oxidation states of cobalt during the photocatalytic reactions. These results shed light on the design concept of new water oxidation catalysts and mechanism-related issues such as the key active intermediate and oxidation state evolution in the oxygen evolution process. The magnetic properties of 1 were also discussed in detail.

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