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Updated: Oct 11, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
Solar-Driven CO2 Reduction Using a Semiconductor/Molecule Hybrid Photosystem: From Photocatalysts to a Monolithic
Takeshi Morikawa1, Shunsuke Sato1, Keita Sekizawa1
1Toyota Central R&D Laboratories., Inc., Nagakute, Aichi 480-1192, Japan.
Abstract:
The synthesis of organic chemicals from H2O and CO2 using solar energy is important for recycling CO2 through cyclical use of chemical ingredients produced from CO2 or molecular energy carriers based on CO2. Similar to photosynthesis in plants, the CO2 molecules are reduced by electrons and protons, which are extracted from H2O molecules, to produce O2. This reaction is uphill; therefore, the solar energy is stored as the chemical bonding energy in the organic molecules. This artificial photosynthetic technology mimicking green vegetation should be implemented as a self-standing system for on-site direct solar energy storage that supports CO2 recycling in a circular economy. Herein, we explain our interdisciplinary fusion methodology to develop hybrid photocatalysts and photoelectrodes for an artificial photosynthetic system for the CO2 reduction reaction (CO2RR) in aqueous solutions. The key factor for the system is the integration of uniquely different functions of molecular transition-metal complexes and solid semiconductors. A metal complex catalyst and a semiconductor appropriate for a CO2RR and visible-light absorption, respectively, are linked, and they function complementary way to catalyze CO2RR under visible-light irradiation as a particulate photocatalyst dispersion in solution. It has also been proven that Ru complexes with bipyridine ligands can catalyze a CO2RR as photocathodes when they are linked with various semiconductor surfaces, such as those of doped tantalum oxides, doped iron oxides, indium phosphides, copper-based sulfides, selenides, silicon, and others. These photocathodes can produce formate and carbon monoxide using electrons and protons extracted from water through potential-matched connections with photoanodes such as TiO2 or SrTiO3 for oxygen evolution reactions (OERs). Benefiting from the very low overpotential of an aqueous CO2RR at metal complexes approaching the theoretical lower limit, the semiconductor/molecule hybrid system demonstrates a single tablet-formed monolithic electrode called "artificial leaf." This single electrode device can generate formate (HCOO-) from H2O and CO2 in a water-filled single-compartment reactor without requiring a separation membrane under unassisted or bias-free conditions, either electrically or chemically. The reaction proceeds with a stoichiometric electron/hole ratio and stores solar energy with a solar-to-chemical energy conversion efficiency of 4.6%, which exceeds that of plants. In this Account, the key results that marked our milestones in technological progress of the semiconductor/molecule hybrid photosystem are concisely explained. These results include design, proof of the principle, and understanding of the phenomena by time-resolved spectroscopies, synchrotron radiation analyses, and DFT calculations. These results enable us to address challenges toward further scientific progress and the social implementation, including the use of earth-abundant elements and the scale-up of the solar-driven CO2RR system.
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