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.
Song et al. (Wed,) studied this question.