Photochemical synthesis and photocatalytic activity in simulated solar light of nanosized Ag doped TiO2 nanoparticle composite

2011 ◽  
Vol 42 (3) ◽  
pp. 579-583 ◽  
Author(s):  
Seonghyuk Ko ◽  
Chandra K. Banerjee ◽  
Jagannathan Sankar
2020 ◽  
Vol 01 ◽  
Author(s):  
S. Akel ◽  
R. Dillert ◽  
D.W. Bahnemann

Aims: cobalt doped TiO2 composites were synthesized with the aim to decrease the TiO2 band gap which results in enhanced visible absorption and then loaded with 1 wt.% of platinum for promoting the formation of molecular hydrogen. Background: Controversial results of the cobalt-based compounds create doubts about the photocatalytic activity of the cobalt doped TiO2 materials. Thus, cobalt doped TiO2 composites were synthesized, and the photocatalytic activity was checked for the hydrogen generation. Objective: The objective of this study is the synthesis of photocatalysts that are highly active for the photocatalytic hydrogen evolution. Methods: The TiO2 and Co-TiO2 photocatalysts were synthesized using two different methods that are reflux and hydrothermal synthesis. Additionally, The Pt deposition on the prepared TiO2 and Co-TiO2 catalysts (1 wt.% Pt) was performed by the photoplatinization method. Result: The results showed that the reduction of protons over bare TiO2 and Co-TiO2 materials is possible from the thermodynamic point of view. The evolution of molecular hydrogen from aqueous methanol employing 1 wt.% platinum loaded on 0.5 wt.% Co-TiO2 photocatalysts under simulated solar light irradiation was investigated. The platinized CoTiO2 composites along with the platinized TiO2 samples have shown high photocatalytic hydrogen evolution. Higher hydrogen evolution rates were determined in the presence of all platinized materials, and a maximum of 317 μmol h-1 is observed on a Pt/Co-TiO2 photocatalyst prepared by a hydrothermal method. Conclusion: EPR results confirmed that the defects observed in the sample prepared within the hydrothermal processing were in the surface and have better crystallinity, while the defects detected on the samples prepared by reflux synthesis were less crystalline. The nature of semiconductor materials was explored through the determination of the flatband potential using the Mott–Schottky equation. The Mott−Schottky analysis of electrochemical impedance measurements showed that all semiconductors were n-type semiconductors and that cobalt doping induces impurity level within the band gap of TiO2. The experimental results of photocatalytic hydrogen generation from methanol-reforming showed that the Co- doping does not affect the photocatalytic activity of both Pt/Co-TiO2 catalysts. Despite that, the Pt/Co-TiO2-HT was the best photocatalyst under simulated solar light and show a maximum hydrogen evolution rate of 317 ± 44 μmol h-1. Other: Based on the experimental results, a possible mechanism for the continuous photocatalytic activity of Pt/Co-TiO2 photocatalysts under simulated solar light is proposed.


2012 ◽  
Vol 509 ◽  
pp. 259-265
Author(s):  
Hao Xie ◽  
Tao Zeng ◽  
Xue Lai Wang ◽  
Xiu Jian Zhao

Three-dimensionally (3D) ordered macroporous ZnO film was fabricated on a glass slide by layer-by-layer depositing and hydrolysis of Zn(CH3COO)2using 3D-ordered latex film as template followed by calcination at 450 °C for 2 h to remove the organic template. The as-prepared 3D-ordered macroporous ZnO film was characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), diffusive reflectance UV-visible absorption spectra (DRUV-VIS), photoluminescence (PL), and photoelectrochemical measurement. Its photocatalytic activity was evaluated by the photocatalytic degradation of crystal violet (CV) aqueous solution at ambient temperature under the irradiation of simulated solar light. It was found that the 3D-ordered ZnO film exhibits efficient photocatalytic activity for photodegradation of CV under the irradiation of simulated solar light.


2015 ◽  
Vol 3 (34) ◽  
pp. 17858-17865 ◽  
Author(s):  
Xiaohong Hu ◽  
Qi Zhu ◽  
Xinlong Wang ◽  
Naoki Kawazoe ◽  
Yingnan Yang

P/Ag/Ag2O/Ag3PO4/TiO2 composite photocatalyst has been successfully prepared by a sol–gel method. It shows highly enhanced photocatalytic ability and stability under simulated solar light irradiation.


2013 ◽  
Vol 807-809 ◽  
pp. 557-561 ◽  
Author(s):  
Wen Tao Yi ◽  
Chun Yan Yan ◽  
Peng Yan ◽  
Shu Yin Liu

AgCl-TiO2 nanocomposites with a core-shell structure were successfully prepared by hydrothermal treatment. And the products were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), Brunauer Emmett teller (BET) Analysis, and UV-vis diffuse reflectance spectroscopy (DRS). It is found that the composites consist of anatase TiO2 and cubic phase AgCl, which has higher surface area, stronger spectral response in visible region compared with pure TiO2. The photocatalytic activity of these samples was evaluated by photocatalytic decoloration of methyl orange (MO) under simulated solar light. The results show AgCl-TiO2 composite has much higher photocatalytic activity than that of pure TiO2, and it also has very good stability. The kinetic study showed that this photocatalytic process coincided with the Langmuir-Hinshelwood (L-H) pseudo first order reaction model.


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