Synthesis and Characterization of the Optical Properties of Pt-TiO2 Nanotubes

Composite Pt-doped TiO2 nanotubes (Pt-TNTs) were synthesized via alkaline fusion-hydrothermal method (AFHM) under ambient atmosphere pressure. Further systematic characterization of Pt-TNTs was performed by using XPS, surface photovoltage spectroscopy (SPS), electric field-induced surface photovolta...

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Bibliographic Details
Main Authors: Zhuwu Jiang, Jingling Li, Wei Liao, Gongduan Fan, Hualiang Yu, Lihong Chen, Zhaoyue Su
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Journal of Nanomaterials
Online Access:http://dx.doi.org/10.1155/2017/6759853
Description
Summary:Composite Pt-doped TiO2 nanotubes (Pt-TNTs) were synthesized via alkaline fusion-hydrothermal method (AFHM) under ambient atmosphere pressure. Further systematic characterization of Pt-TNTs was performed by using XPS, surface photovoltage spectroscopy (SPS), electric field-induced surface photovoltage spectroscopy (FISPS), UV-Vis diffuse reflectance spectrophotometry (UV-Vis), TEM, and XRD. XPS spectrum showed double peaks which accounted for the presence of platinum dioxide and platinum oxide (PtO2 and PtO, PtOxδ+). Composition analysis showed that the particulate matters on surface of Pt-TNTs were composed of PtOxδ+ and TiO2. The results of SPS and FISPS demonstrated that the bound exciton showed sub-band gap transition characteristics with the asymmetric changes of photoelectric property corresponding to changes in polarity and strength of the external electric field. Furthermore, the influence of the changed microstructure morphology of Pt-doped TNTs on both the photovoltage spectroscopy and the lifetime of photogenerated carriers which occurred at the interfaces of Pt-TNTs was observed. Result of XRD indicated that a mixture of anatase and rutile phases prevailed in Pt-TNTs. Contact potential barriers consisting of PtOxδ+, anatase, rutile, and PtOxδ+ are presumed to form upon PtOxδ+ particle that deposited on the surface of Pt-TNTs.
ISSN:1687-4110
1687-4129