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无模板合成三维 Nb(3)O(7)F 分级纳米结构及其增强的光催化活性。

Template-free synthesis of 3D Nb(3)O(7)F hierarchical nanostructures and enhanced photocatalytic activities.

机构信息

State Key Laboratory of Advanced Metallurgy, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing (USTB), Beijing, 100083, PR China.

出版信息

Phys Chem Chem Phys. 2013 Mar 7;15(9):3249-55. doi: 10.1039/c2cp44326k. Epub 2013 Jan 24.

Abstract

Single-crystalline niobium oxide fluoride (Nb(3)O(7)F) hierarchical nanostructures are firstly prepared via a facile hydrothermal method without using any template or surfactant. The results of scanning electron microscopy and transmission electron microscopy showed that the hierarchical morphology of Nb(3)O(7)F could be effectively controlled by adjusting the reaction time. Ultraviolet-visible spectra showed that such nanostructures have a narrow absorption peak at around 400 nm compared to Nb(2)O(5). Based on the first-principles plane-wave ultrasoft pseudo potential (USPP) method, the crystal structures of Nb(3)O(7)F was optimally calculated for the total density of states (TDOS) and the partial density of states (PDOS) of Nb, O and F atoms. According to the observations of architectures formation, a possible growth mechanism was proposed to explain the transformation of nanoparticles to hierarchical nanostructures via an Ostwald ripening mechanism followed by self-assembly. In particular, the excellent photocatalytic activity of the Nb(3)O(7)F hierarchical nanostructures was confirmed by photodegradation of methylene blue, methyl orange and rhodamine B molecules.

摘要

本文首次通过简便的水热法,在不使用任何模板或表面活性剂的情况下制备出了单晶氧化铌氟化物(Nb(3)O(7)F)的分级纳米结构。扫描电子显微镜和透射电子显微镜的结果表明,通过调节反应时间,可以有效地控制 Nb(3)O(7)F 的分级形貌。紫外-可见光谱表明,与 Nb(2)O(5)相比,这种纳米结构在 400nm 左右有一个较窄的吸收峰。基于第一性原理平面波超软赝势(USPP)方法,对 Nb(3)O(7)F 的晶体结构进行了总态密度(TDOS)和 Nb、O 和 F 原子的分态密度(PDOS)的最佳计算。根据结构形成的观察,提出了一个可能的生长机制来解释纳米颗粒到分级纳米结构的转变,这是通过奥斯特瓦尔德熟化机制和自组装来实现的。特别地,通过亚甲基蓝、甲基橙和罗丹明 B 分子的光降解实验,证实了 Nb(3)O(7)F 分级纳米结构具有优异的光催化活性。

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