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分层氮掺杂铌酸铋结构的可控合成及其优异的光催化活性。

Hierarchical nitrogen doped bismuth niobate architectures: controllable synthesis and excellent photocatalytic activity.

机构信息

School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083, China.

出版信息

J Hazard Mater. 2012 May 30;217-218:177-86. doi: 10.1016/j.jhazmat.2012.03.009. Epub 2012 Mar 14.

DOI:10.1016/j.jhazmat.2012.03.009
PMID:22459972
Abstract

Nitrogen doped bismuth niobate (N-Bi(3)NbO(7)) hierarchical architectures were synthesized via a facile two-step hydrothermal process. XRD patterns revealed that the defect fluorite-type crystal structure of Bi(3)NbO(7) remained intact upon nitrogen doping. Electron microscopy showed the N-Bi(3)NbO(7) architecture has a unique peony-like spherical superstructure composed of numerous nanosheets. UV-vis spectra indicated that nitrogen doping in the compound results in a red-shift of the absorption edge from 450nm to 470nm. XPS indicated that [Bi/Nb]N bonds were formed by inducing nitrogen to replace a small amount of oxygen in Bi(3)NbO(7-x)N(x), which is explained by electronic structure calculations including energy band and density of states. Based on observations of architectures formation, a possible growth mechanism was proposed to explain the transformation of polyhedral-like nanoparticles to peony-like microflowers via an Ostwald riping mechanism followed by self-assembly. The N-Bi(3)NbO(7) architectures due to the large specific surface area and nitrogen doping exhibited higher photocatalytic activities in the decomposition of organic pollutant under visible-light irradiation than Bi(3)NbO(7) nanoparticles. Furthermore, an enhanced photocatalytic performance was also observed for Ag/N-Bi(3)NbO(7) architectures, which can be attributed to the synergetic effects between noble metal and semiconductor component.

摘要

氮掺杂铌酸铋(N-Bi(3)NbO(7))分级结构是通过一种简便的两步水热法合成的。XRD 图谱表明,氮掺杂后 Bi(3)NbO(7)的缺陷萤石型晶体结构保持完整。电子显微镜显示,N-Bi(3)NbO(7)结构具有独特的牡丹状球形超结构,由许多纳米片组成。紫外-可见光谱表明,化合物中氮掺杂导致吸收边缘从 450nm 红移到 470nm。XPS 表明,[Bi/Nb]N 键是通过诱导氮取代 Bi(3)NbO(7-x)N(x)中的少量氧形成的,这可以通过电子结构计算包括能带和态密度来解释。基于结构形成的观察,提出了一种可能的生长机制,以解释多面体纳米颗粒通过奥斯特瓦尔德(Ostwald)剥蚀机制转化为牡丹状微花,然后通过自组装。由于具有较大的比表面积和氮掺杂,N-Bi(3)NbO(7)结构在可见光照射下分解有机污染物的光催化活性高于 Bi(3)NbO(7)纳米粒子。此外,Ag/N-Bi(3)NbO(7)结构也表现出增强的光催化性能,这可以归因于贵金属和半导体组分之间的协同效应。

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