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Sensitizing TiO2 nanoparticles with Ru(II) polypyridyl complexes containing anchoring nitrile groups for applications in solar cells
•Sensitization of TiO2 nanoparticles by dyes of ruthenium polypyridyl complexes.•Use of dyes with 1–2 nitrile anchoring units and different electron-donor groups X.•Characterization of Ru/TiO2 electrodes using Raman, UV–Vis and SEM.•DSSC device assembly and characterization by J-V curves and impedan...
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Published in: | Materials letters 2024-09, Vol.371, p.136916, Article 136916 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | •Sensitization of TiO2 nanoparticles by dyes of ruthenium polypyridyl complexes.•Use of dyes with 1–2 nitrile anchoring units and different electron-donor groups X.•Characterization of Ru/TiO2 electrodes using Raman, UV–Vis and SEM.•DSSC device assembly and characterization by J-V curves and impedance measurements.•DSSC efficiency (η) is the best for dyes with 2 nitriles anchors and X = − N(CH3)2.
In this work, five dyes-based on Ru(II) complexes with 2,2́- bipyridyl ligands substituted at the 4,4́-positions with a different number of nitrile anchoring groups and distinct −X electronic donor units were tested as TiO2 electrode sensitizers in solar cells (SCs). All dyes were PF6- salts: three complexes of formulae [Ru(4,4́-(X)2-bpy)2(Mebpy-CN)]2+ with one nitrile group and X = − CH3, –OCH, −N(CH3)2; and two of formulae [Ru(4,4′-(X)2-bpy)(Mebpy-CN)2]2+, with two nitrile units and X = –OCH3, −N(CH3)2. In all cases, bpy = 2,2′-bipyridine and Mebpy-CN = 4-methyl-2,2′-bipyridine-4′-carbonitrile. After characterizing the electrodes morphologically and optically, they were employed in DSSCs (dye-sensitized SCs) using Pt/FTO as counter-electrode (CE) and a KI/I2 in CH3CN as liquid electrolyte. Current density–voltage (J-V) and impedance spectroscopy (IS) measurements highlighted that the SC with the highest efficiency (η) is the one that contains − N(CH3)2 as donor units and two nitrile groups as anchoring entities. It could be concluded that higher electronic delocalization that occurs between the bpys substituted with strong electronic donor groups and the metal orbitals impose excellent properties to improve efficiency, which further improves if two anchoring groups are employed. |
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ISSN: | 0167-577X 1873-4979 |
DOI: | 10.1016/j.matlet.2024.136916 |