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Light induced carbon dioxide reduction by water at binuclear ZrOCoII unit coupled to ir oxide nanocluster catalyst

Authors
Kim, W.Yuan, G.McClure, B.A.Frei, H.
Issue Date
Aug-2014
Publisher
American Chemical Society
Citation
Journal of the American Chemical Society, v.136, no.31, pp 11034 - 11042
Pages
9
Journal Title
Journal of the American Chemical Society
Volume
136
Number
31
Start Page
11034
End Page
11042
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159306
DOI
10.1021/ja504753g
ISSN
0002-7863
1520-5126
Abstract
An all-inorganic polynuclear unit consisting of an oxo-bridged binuclear ZrOCo group coupled to an iridium oxide nanocluster (IrO x) was assembled on an SBA-15 silica mesopore surface. A photodeposition method was developed that affords coupling of the IrO x water oxidation catalyst with the Co donor center. The approach consists of excitation of the ZrOCo metal-to-metal charge-transfer (MMCT) chromophore with visible light in the presence of [Ir(acac)3] (acac: acetylacetonate) precursor followed by calcination under mild conditions, with each step monitored by optical and infrared spectroscopy. Illumination of the MMCT chromophore of the resulting ZrOCo-IrOx units in the SBA-15 pores loaded with a mixture of CO2 and H2O vapor resulted in the formation of CO and O 2 monitored by FT-IR and mass spectroscopy, respectively. Use of O labeled water resulted in the formation of O 2 product. This is the first example of a closed photosynthetic cycle of carbon dioxide reduction by water using an all-inorganic polynuclear cluster featuring a molecularly defined light absorber. The observed activity implies successful competition of electron transfer between the IrOx catalyst cluster and the transient oxidized Co donor center with back electron transfer of the ZrOCo light absorber, and is further aided by the instant deso
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