Issue 44, 2015

Efficient visible light-induced photoelectrocatalytic hydrogen production using CdS sensitized TiO2 nanorods on TiO2 nanotube arrays

Abstract

A novel CdS/TiO2 nanorods/TiO2 nanotube array (CdS/TNRs/TNT) photocatalyst was prepared. The self-organized highly oriented TiO2 nanotube arrays (TNTs) were first synthesized by anodizing Ti sheets. The “flower-like” rutile TiO2 nanorods (TNRs) were then grafted on the TNTs by a hydrothermal method. Subsequently, the CdS quantum dots (CdS QDs) were deposited on the surface of the resulting TNRs/TNTs using a sequential-chemical bath deposition (S-CBD) method. UV-vis diffuse reflectance spectra indicated that the CdS/TNRs/TNTs sample showed significantly enhanced absorption in the range from 350 to 700 nm. The photoelectrocatalytic hydrogen production activities of all samples were evaluated by using Na2S and Na2SO3 as sacrificial reagents in water under a 300 W Xe lamp with a UV-light filter (λ > 420 nm). The results showed that CdS/TNRs/TNTs prepared by hydrothermal reactions for 4 h and S-CBD 15 cycles showed a hydrogen production rate approximately 14 times that of the TNTs. When compared to CdS/TNTs, CdS/TNRs/TNTs showed a 2.3 fold increase in hydrogen production, which can be attributed to the enlarged effective deposition area for CdS QDs by depositing “flower-like” rutile TiO2 nanorods on the TNTs. In addition, CdS/TNRs/TNTs exhibited excellent hydrogen production stability using Na2S and Na2SO3 as sacrificial reagents.

Graphical abstract: Efficient visible light-induced photoelectrocatalytic hydrogen production using CdS sensitized TiO2 nanorods on TiO2 nanotube arrays

Supplementary files

Article information

Article type
Paper
Submitted
07 Jun 2015
Accepted
20 Sep 2015
First published
02 Oct 2015

J. Mater. Chem. A, 2015,3, 22218-22226

Author version available

Efficient visible light-induced photoelectrocatalytic hydrogen production using CdS sensitized TiO2 nanorods on TiO2 nanotube arrays

J. Yu, C. Gong, Z. Wu, Y. Wu, W. Xiao, Y. Su, L. Sun and C. Lin, J. Mater. Chem. A, 2015, 3, 22218 DOI: 10.1039/C5TA04107D

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