Abstract

The efficient and visible-light-active graphitic carbon nitride (gC3N4) has attracted attention for green H2 production from solar energy through water splitting. However, the photocatalyst suffers faster recombination of photogenerated electron-hole pairs and a low visible light absorption efficiency. In this work, the ternary Ag-grafted gC3N4-gC3N4 heterostructures were synthesized using thermal polycondensation of urea and thiourea, followed by photo-deposition of the silver from silver nitrate. The formation of S-scheme heterojunction was confirmed through XRD, VB XPS, UV–Vis, Mott-Schottky, EPR and PL analyses. The X-ray photoelectron spectroscopy revealed the presence of nitrogen vacancies with Ag grafting. The H2 production rate was the highest at 10.1 mmol g−1h−1 with 2.5Ag/gC3N4-gC3N4, which was 3 and 8 times higher than that over gC3N4-gC3N4 and gC3N4, respectively. The addition of Ag mainly contributed to enhance the photocatalytic activity of the heterojunction due to its dual-function. Firstly, silver is attributed to enhance the localized surface plasmon resonance, which broadened the visible light absorption and secondly, the abundant electron capture due to the high Schottky barrier. Moreover, the existence of nitrogen vacancies further improved the separation of charge carriers and helped in carrier transportation. This work provides a new S-scheme heterostructure strategy for the sustainable utilization of solar radiation in the production of H2 from water splitting at higher rates.

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