In-Situ Self-Transformation Growth of Binary g-C3N4/CdS Heterojunctions for Efficient Hydrogen Evolution and Wastewater Treatment
摘要
Developing uniformly dispersed heterojunction photocatalysts with highly coupled interfaces is critical for increasing the photocatalytic efficiency of semiconductor photocatalysts. We used an in-situ self-transformation technique to create an efficient heterojunction photocatalyst from g-C3N4 and CdS. Melamine-CdS composites were used as a precursor in this synthesis. The microscopic observations revealed that CdS nanoparticles were distributed uniformly on the g-C3N4 base. FTIR and XRD spectra ascertained that g-C3N4 and CdS cohabit in the photocatalyst samples. The synthesized binary photocatalysts were used for hydrogen evolution and the degradation of synthetic dyes from wastewater under simulated sunlight irradiation. Rhodamine B and Methyl orange in solution were decomposed under induced visible light exposure. The g-C3N4/CdS showed catalytic dye removal efficiency of 74.03% and 84.03% against methyl orange and Rhodamine B, respectively. During water splitting experiments, g-C3N4/CdS heterojunction showed a reasonable H2 production rate of 2910 µmolh−1 g−1 after five hours of light exposure. The catalytic activity, rate constant, and stability of the composite photocatalyst were significantly higher than pure g-C3N4 and CdS.