Simultaneous integration of the photosensitizer hemin and biocatalyst nanoferrihydrite into a single protein nanocage for selectively photocatalytic CO2 reduction

Abstract

The artificial photoreduction of CO2 into fuels with precious metal-based photosensitizers such as Ru, Re, and Ir represents a potential way to minimize global warming caused by the growing concentration of CO2, but these noble metal-based photosensitizers present unsustainable and negative environmental impact issues, thereby limiting their applications. Herein, bioinspired by the inherent ability of Escherichia coli ferritin (EcBFR) to bind to hemin, we constructed a photocatalytic-CO2-conversion platform by using a single shell-like EcBFR molecule where up to 12 of hemin molecules can be incorporated into its intersubunit interfaces as photosensitizers, while the semiconductor photocatalysts nanoferrihydrites are catalytically synthesized and encapsulated within the protein inner cavity. Consequently, the constructed platform can selectively, effectively reduce CO2 to formic acid with 1-benzyl-1,4-dihydronicotinamide (BNAH) as the electron donor in aqueous solution under mild conditions. To improve the recyclability of the above platform, we designed a three-dimensional (3D) protein crystalline framework with the above constructed hybrid molecules as building blocks through π-π interactions. Notably, such protein framework enables the recyclability to be improved up to at least 5 cycles as compared to the individual protein nanocage. All these findings pave the way for CO2 photoreduction by naturally occurring heme as the photosensitizer in an environmentally friendly manner.