CdS and PbS nanoparticles co-sensitized TiO2 nanotube arrays and their enhanced photoelectrochemical property
•TiO2 nanotube arrays co-sensitized with CdS and PbS nanoparticles were prepared.•CdS and PbS nanoparticles with diameter of 20nm were deposited on TiO2 NTs by SILAR method.•The TiO2 NTs/CdS/PbS exhibited high visible light adsorption, photocurrent density, and the photocatalytic and photoelectrocat...
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Published in | Applied surface science Vol. 315; pp. 149 - 153 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
01.10.2014
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •TiO2 nanotube arrays co-sensitized with CdS and PbS nanoparticles were prepared.•CdS and PbS nanoparticles with diameter of 20nm were deposited on TiO2 NTs by SILAR method.•The TiO2 NTs/CdS/PbS exhibited high visible light adsorption, photocurrent density, and the photocatalytic and photoelectrocatalytic activity.
TiO2 nanotube arrays co-sensitized with CdS and PbS nanoparticles (TiO2 NTs/CdS/PbS) were successfully fabricated by a two-step process of anodization followed by successive ionic layer adsorption and reaction (SILAR) technique. The CdS and PbS nanoparticles grew uniformly on the walls of the TiO2 nanotubes in sequence, and the surface morphology, structure and photoelectrochemical performance of TiO2 NTs/CdS/PbS were investigated and discussed. The results show that the co-sensitization results in an increase in the visible light adsorption, photocurrent density, and photocatalytic and photoelectrocatalytic activity toward degradation of Rhodamine B (RhB). The corresponding mechanism of the TiO2 NTs/CdS/PbS for improving the photoelectrochemical property is tentatively proposed. Co-sensitization of TiO2 NTs by two semiconductors will be an effective way for the development of other high-performance energy-providing materials. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2014.07.116 |