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Photo-catalytic production of hydrogen form ethanol over M/TiO2 catalysts (M = Pd, Pt or Rh)

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TLDR
In this article, the photo-catalytic production of hydrogen from liquid ethanol, a renewable bio-fuel, over Rh/TiO2, Pd/PdO2 and Pt/PtO2 anatase has been studied.
Abstract
The photo-catalytic production of hydrogen from liquid ethanol, a renewable bio-fuel, over Rh/TiO2, Pd/TiO2 and Pt/TiO2, anatase, has been studied. In the absence of the metal, TiO2 shows negligible production of molecular hydrogen. The addition of Pd or Pt dramatically increases the production of hydrogen and a quantum yield of about 10% is reached at 350 K. On the contrary, the Rh doped TiO2 is far less active. The low activity of Rh compared to that of Pd and Pt is not due to poor dispersion or low available Rh sites on the surface, as analyzed by XPS and TEM. For all three catalysts, TEM shows most particles with a size less than 10 nm. XPS results show that while the state of Pd and Pt particles in the as-prepared catalysts was mostly metallic that of the Rh was composed of non-negligible contribution of Rh cations. The extent of reaction of a series of alcohols was also studied, for comparison, on Pt/TiO2. It was found that the reaction is governed by the solvation of the alcohol. In that regard, the production of molecular hydrogen over Pt/TiO2 showed the following trend: methanol ≈ ethanol > propanol ≈ isopropanol > n-butanol.

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A surface science perspective on TiO2 photocatalysis

TL;DR: The field of surface science provides a unique approach to understand bulk, surface and interfacial phenomena occurring during TiO2 photocatalysis as mentioned in this paper, including photon absorption, charge transport and trapping, electron transfer dynamics, adsorbed state, mechanisms, poisons and promoters, and phase and form.
Journal ArticleDOI

The effect of gold loading and particle size on photocatalytic hydrogen production from ethanol over Au/TiO2 nanoparticles

TL;DR: It is demonstrated that Au particles in the size range 3-30 nm on TiO₂ are very active in hydrogen production from ethanol, and the high hydrogen yield observed makes these catalysts promising materials for solar conversion.
Journal ArticleDOI

Photocatalytic hydrogen production using metal doped TiO2: A review of recent advances

TL;DR: In this paper, the basic principles, photocatalytic-reactor design, kinetics, key findings, and the mechanism of metal-doped TiO2 are comprehensively reviewed.
Journal ArticleDOI

Recent Progress in Energy-Driven Water Splitting

TL;DR: This review briefly summarizes thermolytic, electrolytic, photolytic and biolytic water splitting, which highlights photonic and electrical driven water splitting together with photovoltaic‐integrated solar‐driven water electrolysis.
References
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Journal Article

Photoelectrochemical cells : Materials for clean energy

Michael Grätzel
- 01 Jan 2001 - 
TL;DR: In this paper, the authors look into the historical background, and present status and development prospects for photoelectrochemical cells, based on nanocrystalline materials and conducting polymer films.
Journal ArticleDOI

Photoinduced reactivity of titanium dioxide

TL;DR: In this paper, photo-induced superhydrophilicity was used on the surface of a wide-band gap semiconductor like titanium dioxide (TiO 2 ) for photocatalytic activity towards environmentally hazardous compounds.
Book

Practical Surface Analysis

TL;DR: In this paper, the authors used the carbon C 1s peak at 285 eV as a reference for charge correction in XPS analyses of samples prepared outside the high vacuum chamber relatively thick carbon layers are formed on the surfaces.
Journal ArticleDOI

Linear solvation energy relationships. 23. A comprehensive collection of the solvatochromic parameters, .pi.*, .alpha., and .beta., and some methods for simplifying the generalized solvatochromic equation

TL;DR: In this article, a table of donnees (pour de nombreux solvants) des valeurs des parametres M*, α and β donnant respectivement la polarisabilite du solvant, son pouvoir de donneur de proton, and d'accepteur de protons dans les liaisons hydrogene solute-solvant
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