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dc.contributor.author진경석-
dc.contributor.author박지민-
dc.contributor.author이주희-
dc.contributor.author양기동-
dc.contributor.author가젠드라-
dc.contributor.author심욱-
dc.contributor.author정동혁-
dc.contributor.author장해린-
dc.contributor.author박상백-
dc.contributor.author김동훈-
dc.contributor.author성낙언-
dc.contributor.author김선희-
dc.contributor.author한승우-
dc.contributor.author남기태-
dc.date.accessioned2015-12-03T02:08:38Z-
dc.date.available2015-12-03T02:08:38Z-
dc.date.issued201404-
dc.identifier.citationVOL 136, NO 20, 7435-7443-
dc.identifier.issn00027863-
dc.identifier.other45467-
dc.identifier.urihttp://pubs.kist.re.kr/handle/201004/50876-
dc.description.abstractThe development of a water oxidation catalyst has been a demanding challenge in realizing water splitting systems. The asymmetric geometry and flexible ligation of the biological Mn4CaO5 cluster are important properties for the function of photosystem II, and these properties can be applied to the design of new inorganic water oxidation catalysts. We identified a new crystal structure, Mn3(PO4)2·3H2O, that precipitates spontaneously in aqueous solution at room temperature and demonstrated its high catalytic performance under neutral conditions. The bulky phosphate polyhedron induces a less-ordered Mn geometry in Mn3(PO4)2·3H2O. Computational analysis indicated that the structural flexibility in Mn3(PO4)2·3H2O could stabilize the Jahn−Teller-distorted Mn(III) and thus facilitate Mn(II) oxidation. This study provides valuable insights into the interplay between atomic structure and catalytic activity.-
dc.publisherJournal of the American Chemical Society-
dc.subjectWater Splitting-
dc.subjectCatalysis-
dc.subjectBiomimetics-
dc.subjectMn phosphate-
dc.subjectMn structure-
dc.subjectDFT calculation-
dc.titleHydrated Manganese (II) Phosphate (Mn3(PO4)2-3H2O) as a Water Oxidation Catalyst-
dc.typeArticle-
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