Titanium Dioxide Nanotubes as Model Systems for Electrosorption Studies

Highly ordered titanium dioxide nanotubes (TiO<sub>2</sub> NTs) were fabricated through anodization and tested for their applicability as model electrodes in electrosorption studies. The crystalline structure of the TiO<sub>2</sub> NTs was changed without modifying the nanost...

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Main Authors: Li, Xian (Author), Pustulka, Samantha (Author), Pedu, Scott (Author), Xue, Yuan (Author), Richter, Christiaan (Author), Taboada-Serrano, Patricia (Author), Close, Thomas Charles (Contributor)
Format: Article
Language:English
Published: Multidisciplinary Digital Publishing Institute, 2018-06-26T14:54:03Z.
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Online Access:Get fulltext
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100 1 0 |a Li, Xian  |e author 
100 1 0 |a Close, Thomas Charles  |e contributor 
700 1 0 |a Pustulka, Samantha  |e author 
700 1 0 |a Pedu, Scott  |e author 
700 1 0 |a Xue, Yuan  |e author 
700 1 0 |a Richter, Christiaan  |e author 
700 1 0 |a Taboada-Serrano, Patricia  |e author 
700 1 0 |a Close, Thomas Charles  |e author 
245 0 0 |a Titanium Dioxide Nanotubes as Model Systems for Electrosorption Studies 
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856 |z Get fulltext  |u http://hdl.handle.net/1721.1/116618 
520 |a Highly ordered titanium dioxide nanotubes (TiO<sub>2</sub> NTs) were fabricated through anodization and tested for their applicability as model electrodes in electrosorption studies. The crystalline structure of the TiO<sub>2</sub> NTs was changed without modifying the nanostructure of the surface. Electrosorption capacity, charging rate, and electrochemical active surface area of TiO<sub>2</sub> NTs with two different crystalline structures, anatase and amorphous, were investigated via chronoamperometry, cyclic voltammetry, and electrochemical impedance spectroscopy. The highest electrosorption capacities and charging rates were obtained for the anatase TiO<sub>2</sub> NTs, largely because anatase TiO<sub>2</sub> has a reported higher electrical conductivity and a crystalline structure that can potentially accommodate small ions within. Both electrosorption capacity and charging rate for the ions studied in this work follow the order of Cs<sup>+</sup> > Na<sup>+</sup> > Li<sup>+</sup>, regardless of the crystalline structure of the TiO<sub>2</sub> NTs. This order reflects the increasing size of the hydrated ion radii of these monovalent ions. Additionally, larger effective electrochemical active surface areas are required for larger ions and lower conductivities. These findings point towards the fact that smaller hydrated-ions experience less steric hindrance and a larger comparative electrostatic force, enabling them to be more effectively electrosorbed. 
655 7 |a Article 
773 |t Nanomaterials