期刊论文详细信息
Catalysts
CNT-TiO2−δ Composites for Improved Co-Catalyst Dispersion and Stabilized Photocatalytic Hydrogen Production
Peirong Chen3  Lidong Wang1  Ping Wang3  Aleksander Kostka2  Michael Wark3  Martin Muhler3  Radim Beranek1 
[1] Inorganic Chemistry, Ruhr-University Bochum, Universitätstrasse 150, 44780 Bochum, Germany; E-Mail:;Department of Microstructure Physics and Alloy Design, Max-Planck-Institut für Eisenforschung, Max-Planck-Strasse 1, 40237 Düsseldorf, Germany; E-Mail:;Laboratory of Industrial Chemistry, Ruhr-University Bochum, Universitätstrasse 150, 44780 Bochum, Germany; E-Mails:
关键词: carbon nanotubes;    TiO2;    oxygen deficiency;    photocatalytic hydrogen production;    platinum co-catalyst;    stability;   
DOI  :  10.3390/catal5010270
来源: mdpi
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【 摘 要 】

Composites consisting of carbon nanotubes (CNTs) grown directly on oxygen-deficient anatase TiO2 (TiO2−δ) were synthesized by a two-step chemical vapor deposition (CVD) method and applied in photocatalytic hydrogen production from aqueous methanol solutions using photodeposited Pt as the co-catalyst. Thermogravimetry coupled with mass spectroscopy, X-ray diffraction, scanning electron microscopy, photocurrent analysis, X-ray photoelectron spectroscopy, and (scanning) transmission electron microscopy were performed to investigate the physical and (photo)chemical properties of the synthesized CNT-TiO2−δ composites before and after photocatalytic methanol reforming. The initial photocatalytic activity of TiO2 was found to be significantly improved in the presence of oxygen vacancies. An optimized amount (~7.2 wt%) of CNTs grown on the TiO2−δ surface led to a highly effective stabilization of the photocatalytic performance of TiO2−δ, which is attributed to the improved dispersion and stability of the photodeposited Pt co-catalyst nanoparticles and enhanced separation efficiency of photogenerated electron-hole pairs, rendering the photocatalysts less prone to deactivation.

【 授权许可】

CC BY   
© 2015 by the authors; licensee MDPI, Basel, Switzerland.

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