Comparison of the photoelectrochemical performance of particulate and nanotube TiO2 photoanodes

被引:30
|
作者
Chatzitakis, A. [1 ]
Papaderakis, A. [1 ]
Karanasios, N. [2 ]
Georgieva, J. [3 ]
Pavlidou, E. [4 ]
Litsardakis, G. [2 ]
Poulios, I. [1 ]
Sotiropoulos, S. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Chem, Thessaloniki 54124, Greece
[2] Aristotle Univ Thessaloniki, Dept Elect Engn, Thessaloniki 54124, Greece
[3] Bulgarian Acad Sci, Rostislaw Kaischew Inst Phys Chem, Sofia 1113, Bulgaria
[4] Aristotle Univ Thessaloniki, Dept Phys, Thessaloniki 54124, Greece
关键词
TiO2; nanotubes; Sol-gel; Porous electrodes; Electrochemical impedance spectroscopy; Photoelectrocatalytic degradation; Chloramphenicol; SOL-GEL; THIN-FILMS; PHOTOCATALYTIC DEGRADATION; HYDROGEN GENERATION; HETEROGENEOUS PHOTOCATALYSIS; ELECTROCHEMICAL IMPEDANCE; TITANATE NANOTUBES; IMMITTANCE DATA; ARRAYS; ANODIZATION;
D O I
10.1016/j.cattod.2016.07.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this work has been the comparison of the photoelectrocatalytic properties of two types of TiO2-based photoanodes. Sol-gel particulate TiO2 (SGT) layers were grown on Ti substrates (using an isopropoxide precursor) and TiO2 nanotubes (TNTs) were formed by appropriate anodization of the same substrate in glycerin solutions. EIS spectroscopy was employed to determine the intrinsic photoelectrocatalytic activity and surface area of the photoanodes. The intrinsic catalytic activity was assessed by the product R(ct)Q(dl) (where R-ct is the charge transfer resistance). Photovoltammetry experiments showed that the incident photon-to-current efficiency (IPCE) of the TNTs electrodes was 3.5 times higher than that of the SGT ones due to a higher surface area and lower recombination rates. Furthermore, the photoelectrodes were tested against the photoelectrolysis of an antibiotic, where the TNTs showed a 4-fold enhancement in the Chloramphenicol photo-electrolytic degradation rate under +0.5 V reverse bias compared to the SGT. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 20
页数:7
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