No abstract

A metal-free organic semiconductor of mesoporous graphitic carbon nitride (C3N4) coupled with a Ru(II) binuclear complex (RuRu') containing photosensitizer and catalytic units selectively reduced CO2 into HCOOH under visible light (λ > 400 nm) in the presence of a suitable electron donor with high durability, even in aqueous solution. Modification of C3N4 with Ag nanoparticles resulted in a RuRu'/Ag/C3N4 photocatalyst that exhibited a very high turnover number (>33000 with respect to the amount of RuRu'), while maintaining high selectivity for HCOOH production (87-99%). This turnover number was 30 times greater than that reported previously using C3N4 modified with a mononuclear Ru(II) complex, and by far the highest among the metal-complex/semiconductor hybrid systems reported to date. The results of photocatalytic reactions, emission decay measurements, and time-resolved infrared spectroscopy indicated that Ag nanoparticles on C3N4 collected electrons having lifetimes of several milliseconds from the conduction band of C3N4, which were transferred to the excited state of RuRu', thereby promoting photocatalytic CO2 reduction driven by two-step photoexcitation of C3N4 and RuRu'. This study also revealed that the RuRu'/Ag/C3N4 hybrid photocatalyst worked efficiently in water containing a proper electron donor, despite the intrinsic hydrophobic nature of C3N4 and low solubility of CO2 in an aqueous environment.

Highly efficient water oxidation utilizing visible photons of up to 600 nm is a crucial step in artificial photosynthesis. Here we present a highly active photocatalyst for visible-light-driven water oxidation, consisting of single-crystalline meso- and macroporous LaTiO(2)N (LTON) with a band gap of 2.1 eV, and earth-abundasnt cobalt oxide (CoO(x)) as a cocatalyst. The optimized CoO(x)/LTON had a high quantum efficiency of 27.1 ± 2.6% at 440 nm, which substantially exceeds the values reported for previous particulate photocatalysts with a 600-nm absorption edge.