Scinovex
articleTop 1% cited

Hydrogen Production by Photocatalytic Water Splitting over Pt/TiO<sub>2</sub> Nanosheets with Exposed (001) Facets

The Journal of Physical Chemistry C · 2010 · Vol. 114(30) · pp. 13118–13125
Jiaguo YuLifang QiMietek Jaroniec

Abstract

Pt/TiO2 nanosheets with exposed (001) facets were fabricated by a simple hydrothermal route in a Ti(OC4H9)4-HF-H2O mixed solution followed by a photochemical reduction deposition of Pt nanoparticles on TiO2 nanosheets under xenon lamp irradiation. The prepared samples were characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, nitrogen adsorption−desorption isotherms, UV−vis diffuse reflectance spectroscopy, and photoluminescence (PL) spectroscopy. Production of •OH radicals on the TiO2 surface was detected by the PL technique using coumarin as a probe molecule. The effects of Pt loading on the rates of photocatalytic hydrogen production of the as-prepared samples in ethanol aqueous solution were investigated and discussed. The results showed that the photocatalytic hydrogen production rates of TiO2 nanosheets from the ethanol aqueous solutions were significantly enhanced by loaded Pt on the TiO2 nanosheets, and the latter with a 2 wt % of deposited Pt exhibited the highest photocatalytic activity. All fluorinated TiO2 nanosheets exhibited much higher photocatalytic activity than Degussa P25 TiO2 and pure TiO2 nanoparticles prepared in pure water due to the synergistic effect of surface fluorination and exposed (001) facets.

Advanced Photocatalysis TechniquesTiO2 Photocatalysis and Solar CellsCatalytic Processes in Materials SciencePhotocatalysisX-ray photoelectron spectroscopyMaterials scienceAqueous solutionHydrogen productionDiffuse reflectance infrared fourier transformHigh-resolution transmission electron microscopyPhotoluminescenceSpectroscopyCatalysis
Citations
1,160
FWCI
28.98
field-weighted impact
References
61
Percentile
100%
vs. same field & year
Citations per year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.