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Spectral Signatures of Oxidation States in a Manganese-Oxo Cubane Water Oxidation Catalyst
被引:4
|作者:
Mai, Sebastian
[1
]
Klingler, Sarah
[2
]
Trentin, Ivan
[3
]
Kund, Julian
[2
]
Holzer, Marcus
[1
]
Andreeva, Anastasia
[1
]
Stach, Robert
[2
,4
]
Kranz, Christine
[2
]
Streb, Carsten
[3
]
Mizaikoff, Boris
[2
]
Gonzalez, Leticia
[1
]
机构:
[1] Univ Vienna, Fac Chem, Inst Theoret Chem, Wahringer Str 17, A-1090 Vienna, Austria
[2] Ulm Univ, Inst Analyt & Bioanalyt Chem, Albert Einstein Allee 11, D-89081 Ulm, Germany
[3] Ulm Univ, Inst Inorgan Chem 1, Albert Einstein Allee 11, D-89081 Ulm, Germany
[4] Hahn Schickard, Sedanstr 14, D-89077 Ulm, Germany
基金:
奥地利科学基金会;
关键词:
Density functional calculations;
IR spectroscopy;
Polyoxometalates;
UV;
Vis spectroscopy;
Water splitting;
DENSITY-FUNCTIONAL THEORY;
PHOTOSYSTEM-II;
BASIS-SETS;
ENERGY;
APPROXIMATION;
EVOLUTION;
D O I:
10.1002/chem.202102583
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We report IR and UV/Vis spectroscopic signatures that allow discriminating between the oxidation states of the manganese-based water oxidation catalyst [(Mn4O4)(V4O13)(OAc)(3)](3-). Simulated IR spectra show that V=O stretching vibrations in the 900-1000 cm(-1) region shift consistently by about 20 cm(-1) per oxidation equivalent. Multiple bands in the 1450-1550 cm(-1) region also change systematically upon oxidation/reduction. The computed UV/Vis spectra predict that the spectral range above 350 nm is characteristic of the managanese-oxo cubane oxidation state, whereas transitions at higher energy are due to the vanadate ligand. The presence of absorption signals above 680 nm is indicative of the presence of Mn-III atoms. Spectroelectrochemical measurements of the oxidation from [Mn2III Mn2IV ] to [Mn4IV ] showed that the change in oxidation state can indeed be tracked by both IR and UV/Vis spectroscopy.
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页码:17078 / 17086
页数:9
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