A simple preparation method and characterization of B and N co-doped TiO2 nanotube arrays with enhanced photoelectrochemical performance

被引:47
作者
Georgieva, J. [1 ]
Valova, E. [1 ]
Armyanov, S. [1 ]
Tatchev, D. [1 ]
Sotiropoulos, S. [2 ]
Avramova, I. [3 ]
Dimitrova, N. [1 ]
Hubin, A. [4 ]
Steenhaut, O. [4 ]
机构
[1] Bulgarian Acad Sci, Rostislaw Kaischew Inst Phys Chem, Akad G Bonchev Str,Bldg 11, BU-1113 Sofia, Bulgaria
[2] Aristotle Univ Thessaloniki, Dept Chem, Thessaloniki, Greece
[3] Bulgarian Acad Sci, Inst Gen & Inorgan Chem, Sofia, Bulgaria
[4] Vrije Univ Brussel, Res Grp Electrochem & Surface Engn SURF, Sofia, Bulgaria
关键词
TiO2 nanotube arrays (TNTA); B; N-co-doped TNTA; Ti anodization; Photoelectrochemical property; Photoelectrocatalysis; VISIBLE-LIGHT PHOTOCATALYSIS; TITANIA NANOTUBES; ANATASE TIO2; FILMS; OXIDE;
D O I
10.1016/j.apsusc.2017.04.055
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Highly ordered TiO2 nanotube arrays (TNTA) have attracted much attention due to the excellent photocatalytic, optical and electrical properties. However, their absorption range is limited to ultraviolet (UV) spectrum only due to the wide band gap (3.2 eV). One of the strategies to overcome this problem is doping with boron and nitrogen. They are produced via titanium sheet anodization and subsequent electrochemical treatment of titania in an electrolyte containing boric acid. The as-prepared B-TNTA are annealed in N-2 atmosphere at 500 degrees C for 2h to obtain B,N-TNTA. The samples are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV vis diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS). The B,N-TNTA consist of uniform and well aligned nanotubes with an average inner diameter of 80-100 nm and a length not exceeding 1 mu m. The photocurrent response measurements of undoped TNTA, N-doped and B,N-co-doped samples are performed under UV and visible light (Vis) illumination and a comparison is made. The obtained results show that the B,N-doping leads to remarkable photocurrent enhancement and better photocatalytic activity for methyl orange (MO) degradation due to the synergistic effects of B,N-co-doping and lower electron-hole recombination rates. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:284 / 291
页数:8
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