Bi-layered CeO2/SrTiO3 nanocomposite photoelectrode for energy storage and photocathodic protection

被引:40
|
作者
Yang, Yao [1 ]
Cheng, Y. Frank [1 ]
机构
[1] Univ Calgary, Dept Mech & Mfg Engn, Calgary, AB T2N 1N4, Canada
关键词
Photocathodic protection; Energy storage; Bi-layered nanocomposite photoelectrode; Corrosion protection; CORROSION PROTECTION; DOPED TIO2; CEO2; NANOSTRUCTURES; STRONTIUM-TITANATE; CERIUM OXIDE; CARBON-STEEL; THIN-FILMS; SOL-GEL; ANTICORROSION; PERFORMANCE;
D O I
10.1016/j.electacta.2017.09.044
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Photocathodic protection systems have been developed for corrosion control of metals using light energy, rather than supplied direct current or sacrificial anodes. However, one major challenge in photocathodic protection technique is that the anticorrosion performance of the photoelectrochemical response cannot be maintained in the absence of light illumination. This work, at its first time, reports the fabrication of a bi-layered CeO2/SrTiO3 nanocomposite photoelectrode to possess both the energy (photoelectron) storage and photocathodic protection abilities. Various analysis techniques including X-ray diffraction, scanning electron microscopy, energy dispersive spectrum and UV-visible spectroscopy were used to characterize the structure, morphology, composition and photo-response of the prepared photoelectrode. Cyclic voltammetry and electrochemical impedance spectroscopy were used to measure the electrochemical properties. Results demonstrate that the prepared CeO2/SrTiO3 nanocomposite photoelectrode can cathodically polarize the 304 stainless steel for photocathodic protection in 3.5 wt.% NaCl solution under illumination due to the generated photoelectrons by the outer SrTiO3 layer. The inner CeO2 layer can be charged at the photopotential. In the absence of illumination, the photoelectrode can maintain its anticorrosion performance by releasing the stored charges (photoelectrons) in the CeO2 layer to the steel for cathodic polarization. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:134 / 141
页数:8
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