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.
引用
收藏
页码:17078 / 17086
页数:9
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