| Literature DB >> 26919725 |
Laia Francàs1, Craig Richmond1, Pablo Garrido-Barros1, Nora Planas1, Stephan Roeser1, Jordi Benet-Buchholz2, Lluís Escriche2, Xavier Sala2, Antoni Llobet3,4.
Abstract
Three distinct functionalisation strategies have been applied to the in,in-[{Ru(II)(trpy)}2(μ-bpp)(H2O)2](3+) (trpy=2,2':6',2''-terpyridine, bpp=bis(pyridine)pyrazolate) water-oxidation catalyst framework to form new derivatives that can adsorb onto titania substrates. Modifications included the addition of sulfonate, carboxylate, and phosphonate anchoring groups to the terpyridine and bis(pyridyl)pyrazolate ligands. The complexes were characterised in solution by using 1D NMR, 2D NMR, and UV/Vis spectroscopic analysis and electrochemical techniques. The complexes were then anchored on TiO2-coated fluorinated tin oxide (FTO) films, and the reactivity of these new materials as water-oxidation catalysts was tested electrochemically through controlled-potential electrolysis (CPE) with oxygen evolution detected by headspace analysis with a Clark electrode. The results obtained highlight the importance of the catalyst orientation with respect to the titania surface in regard to its capacity to catalytically oxidize water to dioxygen.Entities:
Keywords: organic-inorganic hybrid materials; redox chemistry; ruthenium; supported catalysts; surfaces and interfaces; water splitting
Year: 2016 PMID: 26919725 DOI: 10.1002/chem.201504015
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236