Electrochemical and Photocatalytic Properties of Ru-doped TiO2 Nanostructures for Degradation of Methyl Orange Dye

被引:10
|
作者
Gong, Baoshan [1 ,2 ]
Wu, Pei [1 ,2 ]
Yang, Jia [1 ,2 ]
Peng, Xuanwei [1 ,2 ]
Deng, Hongwen [1 ,2 ]
Yin, Gaohong [1 ,2 ]
机构
[1] Chongqing Univ Sci & Technol, Sch Civil Engn & Architecture, Chongqing 401331, Peoples R China
[2] Environm Protect Res Co Ltd, Chongqing Xin Yun Chuang Inst, Chongqing 402566, Peoples R China
来源
INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE | 2021年 / 16卷 / 02期
关键词
Photodegradation; Methyl orange dye; Ru-doped TiO2; Electrochemical impedance spectroscopy; Degradation efficiency; TITANIUM-DIOXIDE; OPTICAL-PROPERTIES; THIN-FILMS; NANOPARTICLE; PERFORMANCE; DESIGN;
D O I
10.20964/2021.02.18
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This study was focused on chemical synthesis of the pure TiO2 nanorods and Ru-doped TiO2 nanorods and their applications as photocatalyst for photodegradation of the methyl orange (MO) dye under UV and visible irradiations. The morphology, crystallinity, optical, electrochemical and photocatalyst properties of prepared films were characterized by FESEM, XRD, UV-visible absorption, electrochemical impedance spectroscopy (EIS) and photodegradation analyses. The FESEM and XRD studies showed both of films were synthesized in nanorod shape and anatase crystal phase. The optical studies indicate that the optical band gap values were obtained 3.37 eV and 3.22 eV for nanostructured pure TiO2 and Ru-doped TiO2 films, respectively. EIS analysis indicates that Ru-doped TiO2 film exhibited lower recombination rate of photo-excited carriers through effective separation of the photogenerated electron-hole pairs. Photodegradation studies of MO show that the degradation rate significantly was improved by Ru doping and the complete removal of MO were obtained after 55 and 45 minutes under UV and sunlight irradiation, respectively. While, degradation efficiency of MO on pure TiO2 photocatalyst were achieved 57.0 % and 4.8 % after 60 minutes UV and sunlight irradiations, respectively. Therefore, the photodegradation rate of doped film was remarkably enhanced under both UV and sunlight irradiations. Moreover, photocatalytic activity was remarkably promoted under sunlight on doped photocatalyst because of narrowing optical band gaps.
引用
收藏
页码:1 / 12
页数:12
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