In situ Sn2+-incorporation synthesis of titanate nanotubes for photocatalytic dye degradation under visible light illumination

doi:10.1016/j.jallcom.2012.08.081

Chia Nan University of Pharmacy & Science Institutional Repository > 環境永續暨休閒學院 > 環境工程與科學系(所) > 期刊論文 > Item 310902800/27861

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/27861

標題:	In situ Sn2+-incorporation synthesis of titanate nanotubes for photocatalytic dye degradation under visible light illumination
作者:	Tsai, Chien-Cheng Chen, Liang-Che Yeh, Te-Fu Teng, Hsisheng
貢獻者:	環境工程與科學系
關鍵字:	Divalent Sn Ion Photocatalysis Titanate Nanotubes Visible Light
日期:	2013-01
上傳時間:	2014-05-26 10:46:39 (UTC+8)
出版者:	Elsevier Science Sa
摘要:	Sn2+-incorporated titanate nanotubes, prepared by washing a layered sodium titanate with a SnCl2 solution for tube formation, exhibit noticeable photocatalytic activity under visible light irradiation. This in situ synthesis results in a Sn/Ti ratio of approximately 0.6. Because of the introduction of Sn2+ ions, the Sn 5s orbital replaces the O 2p orbital as the top level of the valence band of titanate nanotubes. Optical absorption analysis shows that Sn doping reduces the bandgap of titanate nanotubes from 3.5 to 2.6 eV. Oxidation of the Sn2+-incorporated titanate nanotubes leads to oxidation of Sn2+ to Sn4+, hence, widening the bandgap. Under visible light irradiation, Sn2+-incorporated titanate nanotubes effectively degrade methylene blue in an aqueous solution, whereas the bare titanate nanotubes exhibit substantially lower photocatalytic activity. Photoluminescence analysis demonstrates that the induced charges from excitation of the Sn2+ ions tend to be relaxed through chemical interactions, rather than irradiative recombination. (C) 2012 Elsevier B.V. All rights reserved.
關聯:	Journal of Alloys And Compounds, v.546, pp.95-101
显示于类别:	[環境工程與科學系(所)] 期刊論文

文件中的档案:

档案	描述	大小	格式	浏览次数
index.html		0Kb	HTML	1483	检视/开启

在CNU IR中所有的数据项都受到原著作权保护.

TAIR相关文章

数据加载中.....