首页> 外文期刊>ACS Sustainable Chemistry & Engineering >A General and Facile Approach to Heterostructured Core/Shell BiVO4/BiOI p-n Junction: Room-Temperature in Situ Assembly and Highly Boosted Visible-Light Photocatalysis
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A General and Facile Approach to Heterostructured Core/Shell BiVO4/BiOI p-n Junction: Room-Temperature in Situ Assembly and Highly Boosted Visible-Light Photocatalysis

机译:异质结构核/壳BiVO4 / BiOI p-n结的通用且简便的方法:室温原位组装和高度增强的可见光催化

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摘要

Development of core/shell heterostructures and semiconductor p-n junctions is of great concern for environmental and energy applications. Herein, we develop a facile in situ deposition route for fabrication of a BiVO4/BiOI composite integrating both the core/shell heterostructure and semiconductor p-n junction at room temperature. In the BiVO4/BiOI core/shell heterostructure, the BiOI nanosheets are evenly assembled on the surface of the BiVO4 cores. The photocatalytic performance is evaluated by monitoring the degradation of the dye model Rhodamine B (RhB), colorless contaminant phenol, and photocurrent generation under visible-light irradiation. The heterostructured BiVO4/BiOI core/shell photocatalyst shows drastically enhanced photo-catalysis properties compared to the pristine BiVO4 and BiOI. This remarkable enhancement is attributed to the intimate interfacial interactions derived from the core/shell heterostructure and formation of the p-n junction between the p-type BiOI and n-type BiVO4. Separation and transfer of photogenerated electron-hole pairs are hence greatly facilitated, thereby resulting in the improved photocatalytic performance as confirmed by electrochemical, photoelectrochemical, radicals trapping, and superoxide radical (·O2~-) quantification results. Moreover, the core/shell BiVO4/BiOI also displays high photochemical stability. This work sheds new light on the construction of high-performance photocatalysts with core/shell heterostructures and matchable band structures in a simple and efficient way.
机译:核/壳异质结构和半导体p-n结的开发对于环境和能源应用非常重要。在本文中,我们开发了一种在室温下集成了核/壳异质结构和半导体p-n结的BiVO4 / BiOI复合材料的便捷原位沉积路线。在BiVO4 / BiOI核/壳异质结构中,BiOI纳米片均匀地组装在BiVO4核的表面上。通过监测染料模型若丹明B(RhB),无色污染物苯酚的降解以及在可见光照射下产生的光电流来评估光催化性能。与原始的BiVO4和BiOI相比,异质结构的BiVO4 / BiOI核/壳型光催化剂显示出显着增强的光催化性能。这种显着增强归因于源自核/壳异质结构的亲密界面相互作用以及p型BiOI和n型BiVO4之间p-n结的形成。因此,极大地促进了光生电子-空穴对的分离和转移,从而导致改善的光催化性能,如通过电化学,光电化学,自由基捕获和超氧化物自由基(·O2〜-)定量结果所证实的。此外,核/壳BiVO4 / BiOI也显示出高的光化学稳定性。这项工作为以简单有效的方式构建具有核/壳异质结构和可匹配的能带结构的高性能光催化剂提供了新的思路。

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