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Photodegradation of Unsymmetrical Dimethylhydrazine by TiO(2) Nanorod Arrays Decorated with CdS Nanoparticles Under Visible Light

Photocatalysis technology could utilize solar energy to degrade many toxic pollutants and provides possibility to deal with unsymmetrical dimethylhydrazine (UDMH) wastewater with less energy consumption. In this study, well-aligned TiO(2) nanorod arrays (TiO(2) NRAs) were grown directly on transpare...

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Detalles Bibliográficos
Autores principales: Gao, Xin, Liu, Xiangxuan, Wang, Xuanjun, Zhu, Zuoming, Xie, Zheng, Li, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104699/
https://www.ncbi.nlm.nih.gov/pubmed/27832525
http://dx.doi.org/10.1186/s11671-016-1718-9
Descripción
Sumario:Photocatalysis technology could utilize solar energy to degrade many toxic pollutants and provides possibility to deal with unsymmetrical dimethylhydrazine (UDMH) wastewater with less energy consumption. In this study, well-aligned TiO(2) nanorod arrays (TiO(2) NRAs) were grown directly on transparent conductive glass (FTO) via a hydrothermal method, and TiO(2) NRAs/CdS heterostructure films were prepared by decorating TiO(2) NRAs with CdS nanoparticles through successive ion layer adsorption and reaction (SILAR). Under visible light, the TiO(2) NRAs/CdS heterostructure displays enhanced photodegrading capacity compared with the bare TiO(2) NRAs, and the highest photodegradation rate, 27.5% higher than that of the bare TiO(2) NRAs, was achieved by the sample with 15 SILAR cycles. Additionally, the solution pH had some influence on the degradation process, which shows that the best degradation rate can be achieved in the neutral solution (pH is ca. 7.2), and the photodegradation process can be better in alkaline solution than in the acid solution. Moreover, the visible photocatalytic stability of the TiO(2) NRAs/CdS sample was investigated. Finally, the underlying photocatalytic mechanism was discussed according to the photoelectrochemical and photoluminescence results. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s11671-016-1718-9) contains supplementary material, which is available to authorized users.