This approach improves photocatalytic hydrogenation efficiency in CO2 to methanol, suggesting a method for renewable energy production.
Light-driven methanol synthesis from CO₂ provides a sustainable fuel source and approach to carbon neutralization. Mimicking natural photosynthesis could improve gas-solid photocatalytic efficiency, but it remains highly challenging due to the absence of well-organized mass and charge transfer networks in artificial materials. Herein, we report a chlorophyll-mimicking, nano-pigment nickel gallium oxide, which facilitates discrete light/dark reactions and proton-mediated charge transfer for efficient photocatalytic hydrogenation of CO₂ to methanol. This nano-pigment features surface frustrated Lewis pairs, enabling heterolytic hydrogen splitting into H⁻ and H⁺. The H⁻ acts analogously to nicotinamide adenine dinucleotide phosphate in natural photosynthesis, with Ni(II)/Ni(III) and OH(-I) respectively serving as conduits for ion transport of H⁻ and H⁺ to the Ni site, where they subsequently react with CO₂, mimicking natural carbon fixation. This approach establishes a chlorophyll-mimetic structure for photocatalytic stepwise CO₂ hydrogenation, achieving 3.0% quantum efficiency, 3.20 mmol·h⁻¹·g⁻¹ methanol activity, and 79.6% selectivity.
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Song et al. (2025) studied this question.
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