The Effect of the Heating Rate on Anatase Crystal Orientation and Its Impact on the Photoelectrocatalytic Performance of TiO2 Nanotube Arrays

被引:11
|
作者
Sierra-Uribe, Harrison [1 ]
Maria Cordoba-Tuta, Elcy [1 ,2 ]
Acevedo-Pena, Prospero [3 ]
机构
[1] Univ Ind Santander, Grp Invest Desarrollo & Tecnol Nuevos Mat, Bucaramanga, Colombia
[2] Univ Ind Santander, Grp Invest Minerales Biohidromet & Ambiente, Bucaramanga, Colombia
[3] IPN, CONACyT, Ctr Invest Ciencia Aplicada & Tecnol Avanzada, Unidad Legaria, Mexico City 11500, DF, Mexico
关键词
SENSITIZED SOLAR-CELLS; BARRIER LAYER PROPERTIES; PHOTOELECTROCHEMICAL PROPERTIES; 001; FACETS; ELECTROCHEMICAL PROPERTIES; PHOTOCATALYTIC ACTIVITY; ELECTRON-TRANSPORT; AQUEOUS-MEDIA; FABRICATION; MORPHOLOGY;
D O I
10.1149/2.0241706jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Tuning the degree of anatase crystal orientation in TiO2 nanotube arrays has emerged as a new strategy to control their photoelectrochemical performance, since electron transport through the nanotubular film is favored. However, the existing literature fails to provide an accurate approach to evaluate the impact of anatase crystal orientation, since it is normally studied using TiO2 nanotube films synthesized in different anodizing baths, which in turn affects the properties of the films. In this work, anatase crystal orientation was controlled by changing the heating rate during sample heat-treatment (450 degrees C for 30 min), which resulted in randomly oriented anatase crystals when the film was taken from room temperature to 450 degrees C, to highly crystalline films with preferential anatase crystal orientation when the heating rate was decreased to 5 degrees C min(-1) and 1 degrees C min(-1). Even though the physicochemical properties of the films were almost unaltered, increasing anatase crystal orientation resulted in higher photocurrents and photoelectrocatalytic methyl orange discoloration, showing a maximum for the film treated at a heating rate of 5 degrees C min(-1). (C) 2017 The Electrochemical Society. All rights reserved.
引用
收藏
页码:H279 / H285
页数:7
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