Abstract
A new subporphyrin was synthesized for use as a molecular sensitizer in electrochemical and dye-sensitized photoelectrochemical water oxidation. A photoelectrochemical cell with a TiO2 electrode modified with the sensitizer and a molecular water oxidation catalyst generated higher photocurrent than reference cells that have electrodes modified with either the photosensitizer or the catalyst under visible light (λ > 500 nm) illumination. Oxygen evolution was confirmed after photolysis by GC and GC-MS analyses using isotope-labeling experiments. The large molar extinction coefficients of the ring-contracted porphyrin in the visible region enabled kinetic analysis by time-resolved transient absorption spectroscopy, which also supported the photocatalytic activity.
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