Light induced catalytic and electrochemical enhancement in metal nanoparticles crafted one dimensional TiO2 nanotubes

Author(s):  
Priyanka Bamola ◽  
Saurabh Rawat ◽  
Charu Dwivedi ◽  
Himani Sharma
2017 ◽  
Vol 5 (18) ◽  
pp. 4379-4383 ◽  
Author(s):  
Junais Habeeb Mokkath ◽  
Joel Henzie

Ordered arrangements of metal nanoparticles have attracted significant interest due to their ability to focus and confine light to deeply subwavelength scales.


RSC Advances ◽  
2016 ◽  
Vol 6 (73) ◽  
pp. 68653-68662 ◽  
Author(s):  
Chao Xue ◽  
Xiaoqing Yan ◽  
Shujiang Ding ◽  
Guidong Yang

A novel ternary Ag–AgBr/TiO2 plasmonic nanotube heterojunction photocatalyst was fabricated, showing a very high-performance for decomposition of organic pollutants.


2017 ◽  
Vol 9 (34) ◽  
pp. 28233-28242 ◽  
Author(s):  
Rudolf Kupcik ◽  
Pavel Rehulka ◽  
Zuzana Bilkova ◽  
Hanna Sopha ◽  
Jan M. Macak

Nanoscale ◽  
2013 ◽  
Vol 5 (13) ◽  
pp. 5801 ◽  
Author(s):  
Guanhua Zhang ◽  
Huigao Duan ◽  
Bingan Lu ◽  
Zhi Xu

2009 ◽  
Vol 9 (1) ◽  
pp. 45-49 ◽  
Author(s):  
Xiwang Zhang ◽  
Jia Hong Pan ◽  
Weijiong Fu ◽  
Alan Jiahong Du ◽  
Darren D Sun

Heterogeneous photocatalysis is a promising technology in addressing the incapability of current water technology. In this present paper, we proposed the fabrication of one-dimensional TiO2 nanotubes through hydrothermal method. Various techniques were used to characterize the nanotubes, i.e. FESEM, HRTEM, XRD and BET. Subsequently, the evaluation of photocatalytic oxidative (PCO) properties of TiO2 nanotubes are compared with the commercial TiO2 P25 (i.e. TiO2 powder) in PCO batch reactor. The TiO2 nanotubes show excellent performance with complete photodegradation of humic acid (HA) in comparison with the 97.7% removal efficiency of P25. The TiO2 nanotubes are also tested in membrane filtration for verification of catalyst separation and recovery. The TiO2 nanotubes were totally separated and recovered with membrane filtration. Lastly, its stability is tested in repeated reuse experiments. No catalyst deactivation is observed after five consecutive PCO experiments of newly added HA. Therefore, our novel nanostructured photoctalyst is an advancement in photocatalytic technology that has significant impact for current water technology.


Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1195 ◽  
Author(s):  
Marcin Pisarek ◽  
Piotr Kędzierzawski ◽  
Mariusz Andrzejczuk ◽  
Marcin Hołdyński ◽  
Anna Mikołajczuk-Zychora ◽  
...  

In the present work, the magnetron sputtering technique was used to prepare new catalysts of formic acid electrooxidation based on TiO2 nanotubes decorated with Pt (platinum), Pd (palladium) or Pd + Pt nanoparticles. TiO2 nanotubes (TiO2 NTs) with strictly defined geometry were produced by anodization of Ti foil and Ti mesh in a mixture of glycerol and water with ammonium fluoride electrolyte. The above mentioned catalytically active metal nanoparticles (NPs) were located mainly on the top of the TiO2 NTs, forming ‘rings’ and agglomerates. A part of metal nanoparticles decorated also TiO2 NTs walls, thus providing sufficient electronic conductivity for electron transportation between the metal nanoparticle rings and Ti current collector. The electrocatalytic activity of the TiO2 NTs/Ti foil, decorated by Pt, Pd and/or Pd + Pt NPs was investigated by cyclic voltammetry (CV) and new Pd/TiO2 NTs/Ti mesh catalyst was additionally tested in a direct formic acid fuel cell (DFAFC). The results so obtained were compared with commercial catalyst—Pd/Vulcan. CV tests have shown for carbon supported catalysts, that the activity of TiO2 NTs decorated with Pd was considerably higher than that one decorated with Pt. Moreover, for TiO2 NTs supported Pd catalyst specific activity (per mg of metal) was higher than that for well dispersed carbon supported commercial catalyst. The tests at DFAFC have revealed also that the maximum of specific power for 0.2 Pd/TiO2 catalyst was 70% higher than that of the commercial one, Pd/Vulcan. Morphological features, and/or peculiarities, as well as surface composition of the resulting catalysts have been studied by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), and chemical surface analytical methods (X-ray photoelectron spectroscopy—XPS; Auger electron spectroscopy—AES).


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