Formation and growth of PbO2 inside TiO2 nanotubes for environmental applications

被引:58
作者
Cerro-Lopez, M. [1 ,3 ]
Meas-Vong, Y. [3 ]
Mendez-Rojas, M. A. [2 ]
Martinez-Huitle, C. A. [4 ]
Quiroz, M. A. [1 ]
机构
[1] Univ Las Amer Puebla, Lab Invest Electrocatalisis, Depto Cs Quim Biol, Puebla 72810, Mexico
[2] Univ Las Amer Puebla, Lab Nanotecnol, Depto Cs Quim Biol, Puebla 72810, Mexico
[3] Ctr Invest & Desarrollo Tecnol, Sanfandila 76703, Pedro Escobedo, Mexico
[4] Univ Fed Rio Grande do Norte, Ctr Ciencias Exatas, Depto Quim, BR-59056400 Lagoa Nova Natal, RN, Brazil
关键词
Photoelectrocatalysis; TiO2; nanotubes; PbO2; deposits; Methyl red bleaching; Ti/TiO2; NT-PbO2; anodes; LEAD DIOXIDE ANODE; OXYGEN-TRANSFER REACTIONS; WASTE-WATER TREATMENT; ELECTROCHEMICAL INCINERATION; PHOTOELECTROCATALYTIC DEGRADATION; ELECTROCATALYTIC OXIDATION; ORGANIC POLLUTANTS; AQUEOUS-SOLUTIONS; TITANIUM-OXIDE; OXALIC-ACID;
D O I
10.1016/j.apcatb.2013.07.018
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
The electrodeposition of lead dioxide (PbO2) in a Ti/TiO2 nanotube (TiO2 NT) array was achieved using a galvanostatic method at room temperature. The formation and growth of PbO2 inside the TiO2 NTs was followed as a function of the deposition time (t(d)). The TiO2 NT: :PbO2 (x s) samples, as well as the TiO2 NTs previously prepared by anodization of Ti sheets, were characterized by scanning electronic microscopy (SEM) and X-ray diffraction (XRD) techniques. It was found that PbO2 formation starts at the bottom of TiO2 nanotubes and grows inside them until a well-dispersed deposit is achieved (t(d) < 5 s) or until formation of PbO2 crystalline deposits or cauliflower-like clusters outside the TiO2 NTs at t(d) > 10 s. In any case, the PbO2 deposit always partially covered the TiO2 NT arrays. Photochemical activity results showed that TiO2 NT::PbO2 (x s) samples had higher photocurrent density values than TiO2 NTs. They also had better photoconversion efficiencies, which strongly suggest the occurrence of a photoelectro-synergistic effect due to electronic transfer assisted by the close contact between TiO2 and PbO2. This assumption was supported by the catalytic bleaching of methyl red (MR) dye solutions. Electrocatalytic (EC) and photoelectrocatalytic (PEC) results showed that, although the discoloration process is not entirely PEC dependent, its contribution is greater than the sum of the individual photocatalytic (PC) and EC processes, which confirms the synergic effect produced by the combination of TiO2 and PbO2 in a nanostructured array. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 181
页数:8
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