A precursor-engineering strategy coupled with a microwave molten-salt process (PE-MWMS) is developed to synthesize graphitic carbon nitride (g-C3 N4 ) with an isotype triazine/heptazine-based g-C3 N4 heterojunction as a photocatalyst for the hydrogen evolution reaction (HER) under visible light illumination. Four hybrid precursor combinations-thiourea/melamine, thiourea/dicyandiamide, urea/melamine, and urea/dicyandiamide-are used to synthesize g-C3 N4 heterojunctions by the PE-MWMS process. Control experiments indicate that the precursor components and microwave treatment have a great effect on the HER performance of the g-C3 N4 samples. Samples synthesized with the optimal molar ratios of thiourea/melamine (2:1), thiourea/dicyandiamide (2:1), urea/melamine (3:1), and urea/dicyandiamide (3:1), exhibit the highest HER rates of 3135, 2519, 2844, and 2565 μmol g-1 h-1 , respectively. The amounts of heptazine and triazine units in the g-C3 N4 samples can be easily adjusted by changing the ratios of the hybrid precursors and play a decisive role in improving the photocatalytic HER activity. Because of the unique composition and microstructure, the efficient separation of electron-hole pairs, the broadened photo-absorption edges, and the narrowed band gaps, the as-obtained triazine/heptazine-based g-C3 N4 nanostructures exhibit promising activity for HER application.
Keywords: carbon nitride; heterojunctions; hydrogen evolution; photocatalysis; precursor engineering.
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