Catalytic Reduction of Carbon Monoxide to Liquid Fuels with Recyclable Hydride Donors

Solar light absorption and catalysis are physically separated processes in natural photosynthesis. Natural cofactors, such as nicotinamide adenine dinucleotides (NADH), transport electrons and hydrogen to regulate and activate enzymes at remote locations. The physical separation of light absorption from catalysis provides some inspiration for artificial photosynthesis. One rather extreme implementation is to use copper wires to transport carriers from photovoltaic cells to dark electrodes, where catalysis occurs. Indeed, with a futuristic electrical grid powered solely by photovoltaics, solar capture could be separated from catalysis by hundreds of miles. An alternative approach, that bares more similarity to natural photosynthesis, employs mobile NADH/NAD⁺-like species that shuttle between the light absorber and a proximate, yet unilluminated, location where catalysis occurs. Such a remote approach to solar photocatalysis was recently proposed for the reduction of carbon oxides, CO₂ and CO, to methanol by cascade catalysis. This developing artificial photosynthetic approach offers the promise of catalytic generation of methanol and oxygen gas with sunlight as the sole energy source and CO₂ and water as the only chemical feedstocks. This Viewpoint evaluates the strengths and weaknesses of this approach with an emphasis on CO reduction catalysis with photorecyclable hydride donors while looking forward to what might reasonably be achieved with continued research.

Concepcion, J. J.; Sampaio, R. N.; Meyer, G. J. “Catalytic Reduction of Carbon Monoxide to Liquid Fuels with Recyclable Hydride Donors” ACS Catal., 2024, (14), 16562-16569. https://doi.org/10.1021/acscatal.4c05083