Catalyst-solvent interactions in a dinuclear Ru-based water oxidation catalyst.
Catalyst-solvent interactions in a dinuclear Ru-based water oxidation catalyst.
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DOI:
10.1039/c6dt03789e
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发表时间:
2016-11
影响因子:
4
通讯作者:
A. Shatskiy;R. Lomoth;A. F. Abdel-Magied;Wangchuk Rabten;Tanja M. Laine;Hong Chen;Junliang Sun;P. Andersson;M. Kärkäs;Eric V. Johnston;B. Åkermark
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文献类型:
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作者:
A. Shatskiy;R. Lomoth;A. F. Abdel-Magied;Wangchuk Rabten;Tanja M. Laine;Hong Chen;Junliang Sun;P. Andersson;M. Kärkäs;Eric V. Johnston;B. Åkermark
Photocatalytic water oxidation represents a key process in conversion of solar energy into fuels and can be facilitated by the use of molecular transition metal-based catalysts. A novel straightforward approach for covalent linking of the catalytic units to other moieties is demonstrated by preparation of a dinuclear complex containing two [Ru(pdc)(pic)3]-derived units (pdc = 2,6-pyridinedicarboxylate, pic = 4-picoline). The activity of this complex towards chemical and photochemical oxidation of water was evaluated and a detailed insight is given into the interactions between the catalyst and acetonitrile, a common co-solvent employed to increase solubility of water oxidation catalysts. The solvent-induced transformations were studied by electrochemical and spectroscopic techniques and the relevant quantitative parameters were extracted.