4.7 Article

Synergistic effects of single/multi-walls carbon nanotubes in TiO2 and process optimization using response surface methodology for photo-catalytic H2 evolution

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ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2019.103361

关键词

Photo-catalysis; MW/TiO2/SW Monohybrid; Fast charges separation; Response surface methodology; H-2 evolution

资金

  1. University Technology Malaysia (UTM), Malaysia under RUG (Research University Grant) [Vot 17H06]

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Nobel metals free MW/SW supported TiO2 nanocatalysts were prepared via wet impregnation assisted sol-gel method and tested for photocatalytic H-2 evolution. The photoactivity of TiO2 mediated by MW/SW was considerably improved due to superior charges separation. More importantly, hydrogen production depends on wall numbers such as multiwall or single wall carbon nanotubes, works as electrons acceptor and promoted charges separation. The maximum H-2 evolution rate of 11,060 ppm h(-1) g-cat(-1) was achieved over MW/TiO2/SW, 1.24 folds higher than SW/TiO2 and 1.42 times higher than MW/TiO2 composites. This improved productivity was due to synergistic effects between SW/MW, which greatly promoted charge carriers separations and enables absorption of visible light. Besides, more H-2 production with SW/TiO2 compared to MW/TiO2 was due to more trapping of electrons by single wall than using multi-walls. The activity of composite further enhanced with methanol as hole-scavenger, higher in order of methanol > ethanol > propanol due to presence of a-hydrogen atoms bonded with C-atoms. Response surface methodology (RSM) approach of full factorial design applied to investigate significance and influence of reaction time, loading of catalyst and methanol-water concentration on H-2 yield. The interaction between parameters reveals that catalyst loading has more influence on H-2 evolution compared to other factors. Therefore, this study provides a new approach for noble-metals free synthesis of composite with enhanced visible light H-2 evolution and optimization of parameters for maximum photo-catalytic H-2 production.

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