Particle-assembled SrNbO2N photoanodes were obtained using flux-assisted nitridation reaction. The optimal experimental parameters were studied for SrNbO2N particles with minimum surface defects and high crystallinity.

Graphitic carbon nitride (g-C3N4) has been regarded as an intriguing photocatalyst applying to hydrogen generation but suffering rapid recombination of photoinduced electron-hole pairs and insufficient absorption under visible light. We developed a novel one-pot thermal copolymerization method of melamine as a precursor and 7,7,8,8-tetracyanoquinodimethane (TCNQ) as a comonomer to synthesize modified g-C3N4 (abbreviated as X% TCNQ) for the first time, aiming to directly incorporate TCNQ molecular into carbon nitride skeleton for the substitution of low-electronegative carbon for high-electronegative nitride atom. Results revealed that the as-prepared photocatalysts by copolymerization of melamine with TCNQ retained the original framework of g-C3N4, and dramatically altered the electronic and optical properties of carbon nitride. Various measurements confirmed that as-synthesized samples exhibited larger specific surface areas, faster photogenerated charge transfer and broader optical absorption by decreasing the π-deficiency and extending the π-conjugated system, thus facilitating the photocatalytic activity. Specifically, the 0.3% TCNQ exhibited as high as seven times than the pristine g-C3N4 on photocatalytic H2 generation and kept its photoactivity for five circles. This work highlights a feasible approach of chemical protocols for the molecular design to synthesize functional carbon nitride photocatalysts by copolymerizing appropriate g-C3N4 precursor and comonomers.

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The 5% TCNQ-C3N4 exhibits optimal photoactivity with good stability, which is ascribed to synergistic effects via intermolecular interaction between TCNQ and g-C3N4, with improved optical absorption and promoted separation of photoinduced carriers.