“…Strong photoinduced oxidants are valuable to a range of applications, including solar batteries, − solar-to-fuel devices, − solar-to-electric devices, − and chemical synthesis. , Generating a photoinduced oxidant via interfacial electron transfer to a semiconductor is attractive for many of these applications since interfacial charge separations are often dramatically longer lived than intramolecular charge transfers (milliseconds versus nanoseconds for many organic dyes). − Extending charge separation times is attractive for fundamental studies and for practical applications. The study of chromophores bound to metal oxide semiconductors using visible light to generate oxidants <∼1.0 V versus NHE are well-known through dye-sensitized solar cell and dye-sensitized photoelectrochemical cell literature; ,, however, systems significantly more positive in oxidation potential (>1.5 V versus NHE) are less frequently reported. , Designing chromophores that increase the oxidation potential is an important step toward enabling new visible light driven chemical transformations and using the full potential energy of early visible range photons to give larger potential energy separations of charge which are needed for high-voltage dye-sensitized solar cells (HV DSCs) and multijunction devices, such as sequential series multijunction dye-sensitized solar cells (SSM-DSCs). ,− …”