Electrochemical, spectroelectrochemical and theoretical studies on the reduction and deprotonation of the photovoltaic sensitizer [(H3-tctpy)Ru(NCS)3] (H3-tctpy=2,2′:6′,2′′-terpyridine-4,4′,4′′-tricarboxylic acid) |
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Authors: | Georg Wolfbauer Alan M Bond Glen B Deacon Douglas R MacFarlane Leone Spiccia |
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Abstract: | The electrochemical reduction of the black dye photosensitizer (H3-tctpy)RuII(NCS)3]− (H3-tctpy=2,2′:6′,2′′-terpyridine-4,4′,4′′-tricarboxylic acid) used in photovoltaic cells has been found to be a complex process when studied in dimethylformamide. At low temperatures, fast scan rates and at a glassy carbon electrode, the chemically reversible ligand based one-electron reduction process (H3-tctpy)Ru(NCS)3]−+e−(H3-tctpy√−)Ru(NCS)3]2− is detected. This process has a reversible half-wave potential (Er1/2) of −1585±20 mV versus Fc/Fc+ at 25°C. Under other conditions, a deprotonation reaction occurs upon reduction, which produces (H3−x-tctpyx−)Ru(NCS)3](1+x)− and hydrogen gas. Mechanistic pathways giving rise to the final products are discussed. The Er1/2-value for the ligand based reductions of the deprotonated complex is 0.70 V more negative than for (H3-tctpy)Ru(NCS)3]−. Consequently, data obtained from molecular orbital calculations are consistent with the reaction (H3-tctpy)Ru(NCS)3]−+e−→(H2-tctpy−)Ru(NCS)3]2−+1/2H2 yielding the monodeprotonated complex as the major product obtained after electrochemical reduction of (H3-tctpy)Ru(NCS)3]−. The Er1/2-values for the metal based RuII/III process differ by 0.30 V when data obtained for the protonated and deprotonated forms of the black dye are compared. Electronic spectra obtained during the course of experiments in an optically transparent thin layer electrolysis configuration are consistent with the overall reaction scheme proposed on the basis of voltammetric measurements and molecular orbital calculations. Reduction studies on the free ligand, H3-tcpy, are consistent with results obtained with (H3-tctpy)Ru(NCS)3]−. |
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Keywords: | Photovoltaic sensitizer Reversible potential Cyclic voltammetry Reduction Deprotonation |
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