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具有双重修饰的高效双钒酸铋单晶纳米片:磷掺杂和选择性银修饰。

Highly efficient BiVOsingle-crystal nanosheets with dual modification: phosphorus doping and selective Ag modification.

作者信息

Fu Can, Xu Baoyun, Dong Lingling, Zhai Jinguo, Wang Xuefei, Wang De-Yi

机构信息

IMDEA Materials Institute, E-28906 Getafe, Madrid, Spain.

E.T.S. de Ingenieros de Caminos, Universidad Politécnica de Madrid, E-28040 Madrid, Spain.

出版信息

Nanotechnology. 2021 May 17;32(32). doi: 10.1088/1361-6528/abfc0b.

DOI:10.1088/1361-6528/abfc0b
PMID:33906165
Abstract

BiVO, a visible-light response photocatalyst, has shown tremendous potential because of abundant raw material sources, good stability and low cost. There exist some limitations for further applicaitions due to poor capability to separate electron-hole pairs. In fact, a single-component modification strategy is barely adequate to obtain highly efficient photocatalytic performance. In this work, P substituted some of the V atoms from VOoxoanions, namely P was doped into the V sites in the host lattice of BiVOby a hydrothermal route. Meanwhile, Ag as an attractive and efficient electron-cocatalyst was selectively modified on the (010) facet of BiVOnanosheets via facile photo-deposition. As a result, the obtained dually modified BiVOsheets exhibited enhanced photocatalytic degradation property of methylene blue (MB). In detail, photocatalytic rate constant () was 2.285 ming, which was 2.78 times higher than pristine BiVOnanosheets. Actually, P-doping favored the formation of O vacancies, led to more charge carriers, and facilitated photocatalytic reaction. On the other hand, metallic Ag loaded on (010) facet effectively transferred photogenerated electrons, which consequently helped electron-hole pairs separation. The present work may enlighten new thoughts for smart design and controllable synthesis of highly efficient photocatalytic materials.

摘要

BiVO₄是一种可见光响应光催化剂,因其原料来源丰富、稳定性好且成本低而展现出巨大潜力。由于电子 - 空穴对分离能力差,其进一步应用存在一些局限性。事实上,单一组分改性策略几乎不足以获得高效的光催化性能。在这项工作中,P取代了VOₓ氧阴离子中的一些V原子,即通过水热法将P掺杂到BiVO₄主体晶格的V位点中。同时,Ag作为一种有吸引力的高效电子助催化剂,通过简便的光沉积法选择性地修饰在BiVO₄纳米片的(010)晶面上。结果,所获得的双重改性BiVO₄纳米片表现出增强的亚甲基蓝(MB)光催化降解性能。具体而言,光催化速率常数(k)为2.285 min⁻¹,比原始BiVO₄纳米片高2.78倍。实际上,P掺杂有利于O空位的形成,导致更多的电荷载流子,并促进光催化反应。另一方面,负载在(010)晶面上的金属Ag有效地转移了光生电子,从而有助于电子 - 空穴对的分离。本工作可能为高效光催化材料的智能设计和可控合成提供新思路。

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