An Exceptionally Efficient Co-Co P@N, P-Codoped Carbon Hybrid Catalyst for Visible Light-Driven CO -to-CO Conversion.

Artificial photosynthesis has attracted wide attention, particularly the development of efficient solar light-driven methods to reduce CO to form energy-rich carbon-based products. Because CO reduction is an uphill process with a large energy barrier, suitable catalysts are necessary to achieve this transformation. In addition, CO adsorption on a catalyst and proton transfer to CO are two important factors for the conversion reaction, and catalysts with high surface area and more active sites are required to improve the efficiency of CO reduction. Here, a visible light-driven system for CO -to-CO conversion is reported, which consists of a heterogeneous hybrid catalyst of Co and Co P nanoparticles embedded in carbon nanolayers codoped with N and P (Co-Co P@NPC) and a homogeneous Ru -based complex photosensitizer. The average generation rate of CO of the system was up to 35 000 μmol h  g with selectivity of 79.1 % in 3 h. Linear CO production at an exceptionally high rate of 63 000 μmol h  g was observed in the first hour of reaction. Inspired by this highly active catalyst, Co@NC and Co P@NPC materials were also synthesized and their structure, morphology, and catalytic properties for CO photoreduction were explored. The results showed that the nanoparticle size, partially adsorbed H O molecules on the catalyst surface, and the hybrid nature of the systems influenced their photocatalytic CO reduction performance.