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Автор Brennan, Bradley J
Автор Keirstead, Amy E
Автор Liddell, Paul A
Автор Vail, Sean A
Автор Moore, Thomas A
Автор Moore, Ana L
Автор Gust, Devens
Дата выпуска 2009-12-16
dc.description A triethanolamine-protected silane, 1-(3′-amino)propylsilatrane, was incorporated into the structure of porphyrin- and ruthenium-based dyes and used to link them to transparent semiconductor nanoparticulate metal oxide films. Silatrane reacts with the metal oxide to form strong, covalent silyl ether bonds. In this study, silatrane-functionalized dyes and analogous carboxylate-functionalized dyes were used as visible light sensitizers for porous nanoparticulate SnO<sub>2</sub> photoanodes. The performance of the dyes was compared in photoelectrochemical cells incorporating either non-regenerative or regenerative redox components. The non-regenerative cell used NADH (β-nicotinamide adenine dinucleotide) as a sacrificial electron donor and Hg<sub>2</sub>SO<sub>4</sub>/Hg as a sacrificial cathode, whereas the regenerative cell used the iodide/triiodide redox couple. Experiments showed that the silyl ether bonding gave the electrodes increased stability toward sensitizer desorption compared to carboxylate surface linkages. Porphyrin-silatrane dyes also demonstrated similar or better performance than their carboxylate analogs in photoelectrochemical cells. The improvement correlates with the results from transient absorbance spectroscopy, which show that the longer linker on the silatrane porphyrins slows charge recombination between oxidized porphyrin and the electrode surface. The improved photoelectrochemical cell efficiency and stability of the silatrane-based dyes compared to carboxylates demonstrate that silatranes are promising agents for bonding organic molecules to metal oxide surfaces.
Формат application.pdf
Издатель Institute of Physics Publishing
Копирайт IOP Publishing Ltd
Название 1-(3′-amino)propylsilatrane derivatives as covalent surface linkers to nanoparticulate metal oxide films for use in photoelectrochemical cells
Тип paper
DOI 10.1088/0957-4484/20/50/505203
Electronic ISSN 1361-6528
Print ISSN 0957-4484
Журнал Nanotechnology
Том 20
Первая страница 505203
Последняя страница 505212
Аффилиация Keirstead, Amy E;
Аффилиация Moore, Thomas A;
Аффилиация Moore, Ana L;
Аффилиация Gust, Devens;
Аффилиация Brennan, Bradley J; Department of Chemistry and Biochemistry, Center for Bioenergy and Photosynthesis, Arizona State University, Tempe, AZ 85287, USA
Аффилиация Liddell, Paul A; Department of Chemistry and Biochemistry, Center for Bioenergy and Photosynthesis, Arizona State University, Tempe, AZ 85287, USA
Аффилиация Vail, Sean A; Department of Chemistry and Biochemistry, Center for Bioenergy and Photosynthesis, Arizona State University, Tempe, AZ 85287, USA
Выпуск 50

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