Enhanced photocatalytic degradation of Congo red by a BiVO4/ZnIn2S4 composite: performance and mechanism
Abstract
High-performance visible-light-driven photocatalysts have emerged as a research hotspot in environmental pollution; however, the photocatalytic degradation mechanisms of Congo red using bismuth semiconductor composites are not fully understood. Herein, BiVO4/ZnIn2S4 was successfully synthesized via a hydrothermal method, and the photocatalytic performance of the composite was assessed by carrying out photocatalysis experiments to decompose Congo red. The phase composition, carrier separation capability, interface electron interactions, and morphological features were characterized by XRD, PL, XPS, and TEM analyses, respectively. The results showed that a Z-scheme heterostructure was successfully constructed between the BiVO4 and ZnIn2S4. Electrons in the conduction band of BiVO4 migrated to the valence band of ZnIn2S4, which effectively enhanced the separation of photogenerated charge carriers and improved the degradation capability. Compared with pure BiVO4, 7% BiVO4/ZnIn2S4 displayed superior photocatalytic capability and could completely remove Congo red (100 mg L−1) in 60 min under visible light. Radical trapping experiments combined with electron paramagnetic resonance characterization revealed that the superoxide anion (˙O2−) and holes (h+) acted as the key reactive species driving Congo red degradation. In addition, six cycles of experiments were performed to verify that the BiVO4/ZnIn2S4 composite retains its high stability. This study provides a feasible strategy for fabricating effective photocatalysts to treat organic pollutants in wastewater.

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