Completing a Charge Transport Chain for Artificial Photosynthesis

• Published in: Journal of the American Chemical Society 2018-08, Vol.140 (31), p.9823-9826
• Main Authors: Eberhart, Michael S, Bowers, Leah M. Rader, Shan, Bing, Troian-Gautier, Ludovic, Brennaman, M. Kyle, Papanikolas, John M, Meyer, Thomas J
• Format: Article
• Language: English
• Subjects: catalysis (heterogeneous); catalysis (homogeneous); charge transport; electrodes - solar; hydrogen and fuel cells; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; materials and chemistry by design; photosynthesis (natural and artificial); solar (fuels); solar (photovoltaic); synthesis (novel materials); synthesis (self-assembly)
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.8b06740

A ruthenium polypyridyl chromophore with electronically isolated triarylamine substituents has been synthesized that models the role of tyrosine in the electron transport chain in photosystem II. When bound to the surface of a TiO2 electrode, electron injection from a Ru­(II) Metal-to-Ligand Charge Transfer (MLCT) excited state occurs from the complex to the electrode to give Ru­(III). Subsequent rapid electron transfer from the pendant triarylamine to Ru­(III) occurs with an observed rate constant of ∼1010 s–1, which is limited by the rate of electron injection into the semiconductor. Transfer of the oxidative equivalent away from the semiconductor surface results in dramatically reduced rates of back electron transfer, and a long-lived (τ = ∼165 μs) triarylamine radical cation that has been used to oxidize hydroquinone to quinone in solution.