Synergistic oxygen substitution and heterostructure construction in polymeric semiconductors for efficient water splitting

Herein, we present a synergistic oxygen-substitution and heterostructure construction strategy to produce a two-dimensional oxygenated-triazine-heptazine-conjugated carbon nitride nanoribbon (TOH-CN). The TOH-CN was proved to have an internal donor-acceptor heterostructure that could promote interfacial charge separation and transport, while the oxygen substitution effect modulated the nanoribbon morphology with increased surface/edge active sites and tuned the electronic structure to extend visible-light absorption as well as to improve band structure alignment. Benefiting from these advantages, the TOH-CN served as an efficient bifunctional photocatalyst for both H 2 and O 2 evolution under visible-light irradiation, exhibiting a 16 times higher photocatalytic H 2 evolution rate than that of its melon-based carbon nitride (g-C 3 N 4 ) counterpart, and a remarkable apparent quantum yield of 7.9% at 420 nm. The O 2 evolution rate was 6 times higher than that of g-C 3 N 4 , even much higher than those of most bifunctional carbon nitride-based photocatalysts. The developed synergistic strategy of oxygen substitution and heterostructure construction will provide an alternative route for the synthesis of efficient polymeric semiconductors toward efficient solar-to-chemical conversion. A synergistic oxygen substitution and heterostructure construction strategy was developed to synthesize oxygenated-triazine-heptazine-conjugated polymer nanoribbons for photocatalytic water splitting.