期刊
ACS APPLIED NANO MATERIALS
卷 4, 期 3, 页码 3262-3272出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c00481
关键词
BiVO4; BiOCl; BiOI; BiOBr; halide effects; Pd; photocatalysis
资金
- National Science Foundation [1903649]
- University of Miami
- Ball State University
- Sylvester Comprehensive Cancer Center
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1903649] Funding Source: National Science Foundation
In this study, nanoscale BiVO4/BiOX/Pd materials were successfully synthesized using a single pot approach, and the effect of halide identity on photocatalytic properties was investigated. Results showed that BiOCl and BiOBr structures exhibited enhanced reactivity compared to BiOI, with potential environmental applications demonstrated in degradation experiments using natural water samples.
In this contribution, a single pot approach was employed to synthesize nanoscale BiVO4/BiOX/Pd, where the halogen was varied over Cl, Br, and I. These materials were used to study the effect of the halide identity in the BiOX nanoplate component for its ability to modulate/maximize the photocatalytic properties of the materials. Once the nanomaterials were fully characterized via a suite of approaches, their reactivity for the degradation of rhodamine B, a model pollutant, was examined. All of the materials demonstrated high photocatalytic rates, reaching completion in <10 min in most cases. The results demonstrated that the BiVO4/BiOCl/Pd and BiVO4/BiOBr/Pd have significantly enhanced reactivity compared to the BiVO4/BiOI/Pd structures. Further studies using the BiVO4/BiOBr/Pd in the degradation of rhodamine B in natural water samples indicated that the materials retained their reactivity, demonstrating their potential use in environmental systems.
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