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Ruthenium(ii)-polypyridyl zirconium(iv) metal–organic frameworks as a new class of sensitized solar cells
A series of Ru(ii)L(2)L′ (L = 2,2′-bipyridyl, L′ = 2,2′-bipyridine-5,5′-dicarboxylic acid), RuDCBPY, -containing zirconium(iv) coordination polymer thin films have been prepared as sensitizing materials for solar cell applications. These metal–organic framework (MOF) sensitized solar cells, MOFSCs,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953006/ https://www.ncbi.nlm.nih.gov/pubmed/29896356 http://dx.doi.org/10.1039/c5sc01565k |
Sumario: | A series of Ru(ii)L(2)L′ (L = 2,2′-bipyridyl, L′ = 2,2′-bipyridine-5,5′-dicarboxylic acid), RuDCBPY, -containing zirconium(iv) coordination polymer thin films have been prepared as sensitizing materials for solar cell applications. These metal–organic framework (MOF) sensitized solar cells, MOFSCs, each are shown to generate photocurrent in response to simulated 1 sun illumination. Emission lifetime measurements indicate the excited state quenching of RuDCBPY at the MOF–TiO(2) interface is extremely efficient (>90%), presumably due to electron injection into TiO(2). A mechanism is proposed in which RuDCBPY-centers photo-excited within the MOF-bulk undergo isotropic energy migration up to 25 nm from the point of origin. This work represents the first example in which a MOFSC is directly compared to the constituent dye adsorbed on TiO(2) (DSC). Importantly, the MOFSCs outperformed their RuDCBPY–TiO(2) DSC counterpart under the conditions used here and, thus, are solidified as promising solar cell platforms. |
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