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A Ru-Co hybrid material based on a molecular photosensitizer and a heterogeneous catalyst for light-driven water oxidation
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Molecular Biomimetics.
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2014 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 16, no 8, 3661-3669 p.Article in journal (Refereed) Published
Abstract [en]

A novel approach to anchor a molecular photosensitizer onto a heterogeneous water oxidation catalyst via coordination bonds is presented. A photosensitizer (1) based on [Ru(bpy)(3)](2+) and decorated with two methylenediphosphonate (M2P) groups has been designed and synthesized for this purpose. The M2P groups in complex 1 allow for coordination of cobalt ions to afford a novel molecular-heterogeneous hybrid material P1. Scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS) were used to characterize P1 as an amorphous, non-uniform material that contains Ru and Co in a ratio of 1:2. A suspension of P1 in a buffered aqueous solution is active as a light-driven water oxidation catalyst in the presence of persulfate (S2O82-) as electron acceptor. The yield of oxygen is higher when P1 is prepared in situ by mixing and illuminating 1 and Co2+ in the presence of S2O82-. After oxygen evolution ceases, a second material P2 can be isolated from the reaction mixture. P2 is characterized by a lower Ru content than P1, and contains Co in a higher oxidation state. Interestingly, P2 as a freshly prepared suspension is also active for light-driven water oxidation. It is shown that 1 resides in the interior of P1 and P2, and is thus in a location where undesirable quenching pathways of the photo-excited state of 1 limit the oxygen production yields for both P1 and P2.

Place, publisher, year, edition, pages
2014. Vol. 16, no 8, 3661-3669 p.
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Chemical Sciences
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URN: urn:nbn:se:uu:diva-220935DOI: 10.1039/c3cp54500hISI: 000330779700036OAI: oai:DiVA.org:uu-220935DiVA: diva2:707373
Available from: 2014-03-24 Created: 2014-03-24 Last updated: 2017-12-05Bibliographically approved

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Liu, JiaZhu, JiefangStyring, StenbjornOtt, SaschaThapper, Anders

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