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Tuneable Phase, Morphology, and Performance of Bismuth Oxyhalide Photocatalysts via Microwave-Assisted Synthesis

光催化 材料科学 形态学(生物学) 化学工程 相(物质) 微波食品加热 纳米技术 催化作用 有机化学 光电子学 冶金 化学 电信 生物 计算机科学 遗传学 工程类
作者
Melissa Marks,Henrik S. Jeppesen,Nina Lock
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (20): 23496-23506 被引量:33
标识
DOI:10.1021/acsami.2c03837
摘要

In this study, a facile microwave-assisted synthesis approach was used to produce a series of bismuth oxyhalide photocatalysts, with systematic changes in synthesis pH between 1 and 14 allowing control over a broad range of material properties and characteristics. Detailed structural and morphological investigations with powder X-ray diffraction (PXRD), Rietveld refinements, pair distribution function (PDF) analysis, and scanning electron microscopy (SEM) show that thin particles of BiOCl, BiOBr, Bi24O31Cl10, and Bi24O31Br10 were selectively produced, with progressive changes in morphology, facet dominance, and phase as a function of pH. The impact of these changes on photocatalytic performance was evaluated by studying the aerobic oxidation of benzylamine to N-benzylidenebenzylamine, with all materials exhibiting photocatalytic abilities under UV or blue light. While a combination of material properties and characteristics influenced the photocatalytic performance, certain factors such as surface area, facet dominance, amorphous content, and band gap were found to have a larger impact on the photocatalytic yield. Overall, this study demonstrates the possibilities of phase, morphology, and performance of bismuth oxyhalide photocatalysts over the entire pH range, produced using a fast and facile microwave-assisted synthesis technique as an alternative to the more widely applied hydrothermal synthesis approach. Additionally, the detailed structural and morphological investigations of the materials contribute to a greater understanding of bismuth oxyhalide photocatalysts in general, while also highlighting some of the most desirable properties for improved photocatalytic performance of these materials.
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