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具有增强可见光光催化活性的Ag3PO4/TiO2纳米管异质结的原位制备。

In situ fabrication of Ag3PO4/TiO2 nanotube heterojunctions with enhanced visible-light photocatalytic activity.

作者信息

Tong Zhen Wei, Yang Dong, Sun Yuan Yuan, Tian Yao, Jiang Zhong Yi

机构信息

Key Laboratory for Green Technology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.

出版信息

Phys Chem Chem Phys. 2015 May 14;17(18):12199-206. doi: 10.1039/c4cp05851h.

Abstract

Ag3PO4/TiO2 nanotube (TNT) heterojunctions were fabricated via a facile in situ growth method. Hemispherical Ag3PO4 nanocrystals were uniformly grown on the TNT surface, and their size was confined to 5-10 nm. A joint area was distinctly observed between the Ag3PO4 nanocrystals and TNT, indicating the formation of a Ag3PO4/TNT heterojunction. Compared with pure Ag3PO4, the Ag3PO4/TNT heterojunction possesses more active sites, less bulk defects, more efficient electron-hole separation, as well as better dye adsorption properties, and thus exhibits a significantly elevated photocatalytic activity for Rhodamine B (RhB) degradation. The study of the reactive species demonstrates that the photocatalytic degradation of RhB over the Ag3PO4/TNT heterojunction is primarily driven by both photogenerated h(+) and ˙OH radicals. This easily-fabricated Ag3PO4/TNT heterojunction with promising photocatalytic activity may find potential applications in energy and environmental related areas.

摘要

通过一种简便的原位生长方法制备了Ag3PO4/TiO2纳米管(TNT)异质结。半球形的Ag3PO4纳米晶体均匀地生长在TNT表面,其尺寸限制在5-10纳米。在Ag3PO4纳米晶体和TNT之间明显观察到一个结合区域,表明形成了Ag3PO4/TNT异质结。与纯Ag3PO4相比,Ag3PO4/TNT异质结具有更多的活性位点、更少的体缺陷、更有效的电子-空穴分离以及更好的染料吸附性能,因此对罗丹明B(RhB)降解表现出显著提高的光催化活性。对反应物种的研究表明,Ag3PO4/TNT异质结上RhB的光催化降解主要由光生h(+)和˙OH自由基驱动。这种易于制备且具有良好光催化活性的Ag3PO4/TNT异质结可能在能源和环境相关领域找到潜在应用。

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