Enhanced photocatalytic performance of poly(3,4-ethylenedioxythiophene)-coated TiO2 nanotube electrodes

被引:9
|
作者
Abdelnasser, Shady [1 ]
Park, Geunsu [2 ]
Han, Hyunwoo [2 ]
Toth, Rita [3 ]
Yoon, Hyeonseok [2 ,4 ]
机构
[1] Amer Univ Cairo, Dept Mech Engn, AUC Ave,POB 74, New Cairo 11835, Egypt
[2] Chonnam Natl Univ, Dept Polymer Engn, Grad Sch, 77 Yongbong Ro, Gwangju 61186, South Korea
[3] Swiss Fed Labs Mat Sci & Technol, Lab High Ceram, EMPA, CH-8600 Dubendorf, Switzerland
[4] Chonnam Natl Univ, Sch Polymer Sci & Engn, 77 Yongbong Ro, Gwangju 61186, South Korea
基金
新加坡国家研究基金会; 瑞士国家科学基金会;
关键词
Conducting polymers; Nanotubes; Charge transport; Energy conversion; SOLAR HYDROGEN-PRODUCTION; VISIBLE-LIGHT; NANOWIRE ARRAYS; WATER; NITROGEN; FILMS; NANOMATERIALS; BEHAVIOR; INDIUM;
D O I
10.1016/j.synthmet.2019.03.018
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study presents the design of a mixed organic-inorganic system to be utilized in solar-light chemical energy conversion applications, where the visible-light absorption properties of the conducting polymer, poly(3,4-ethylenedioxythiophene) (PEDOT), are combined with the enhanced charge transport properties of TiO2 nanotubes, thus creating an efficient photoelectrode. A dispersion of PEDOT doped with p-toluenesulfonate (tosylate) ions was synthesized using a simple solution-casting polymerization process, which was then spin-coated onto an ordered array of anodically fabricated TiO2 nanotubes to be used for solar energy conversion. Electron microscopy observation confirmed the presence of PEDOT in the hybrid (PEDOT-TiO2) and Fourier transform infrared spectroscopy verified the vibrational modes of the polymerized PEDOT. The ultraviolet-visible diffuse reflectance data indicated a change in the absorption edge of the pure TiO2 nanotubes to longer wavelengths after PEDOT coating. The developed photo-electrodes exhibited a significant increase in photocurrent response and lower charge transfer resistance with respect to the pure TiO2 nanotubes, as verified by electrochemical impedance spectroscopy.
引用
收藏
页码:120 / 126
页数:7
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