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Photoassisted hydrogen evolution over spinel CuM2O4 (M = Al, Cr, Mn, Fe and Co)

Identifieur interne : 000870 ( Main/Exploration ); précédent : 000869; suivant : 000871

Photoassisted hydrogen evolution over spinel CuM2O4 (M = Al, Cr, Mn, Fe and Co)

Auteurs : S. Saadi [Algérie] ; A. Bouguelia [Algérie] ; M. Trari [Algérie]

Source :

RBID : Pascal:06-0474176

Descripteurs français

English descriptors

Abstract

The photocatalytic ability of CuM2O4 (M = Al, Cr, Mn, Fe and Co) crystallizing with spinel-type structure has been evaluated according to the H2-evolution. The oxides are black and displayed a semiconducting behavior where the electronic balance comes from a small over stochiometry (CuCo2O4.016). Electron hopping occurs between similar sites in normal spinel with a low activation energy whereas larger energies were found in inverse spinel. The electrodes were characterized photoelectrochemically and acquired the characteristic of p-type semiconductors. The conduction band edge, determined from intensity-potential curves, is located below the H2O/H2 potential leading to a thermodynamically favorable H2-liberation under visible light. The photoactivity was dependent on preparative conditions and the best results were obtained over CuCo2O4 prepared through nitrate route in presence of SO2-3 (3.6mlh-1g-1). Improved photoactivity may be interpreted in terms of flat band potential and electronegativity. The presence of cobalt contributes to increase the electron affinity, a desirable property for p-type specimen. It has been observed that the amount of evolved H2 rose using stronger reductors by increasing the band bending. The initial performance of catalyst was almost restored using a fresh reactant solution. With time, the water reduction slowed down because the end products S2-n and S2O2-6 compete with the adsorbed water for the photoelectrons.


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Le document en format XML

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<term>Nitrates</term>
<term>Optimization</term>
<term>Photocatalysis</term>
<term>Renewable energy</term>
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<term>Nitrate</term>
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<term>Photocatalyse</term>
<term>Spinelle</term>
<term>Semiconducteur type p</term>
<term>Etude expérimentale</term>
<term>Diffractométrie RX</term>
<term>Cuivre Cobalt Oxyde</term>
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<front>
<div type="abstract" xml:lang="en">The photocatalytic ability of CuM
<sub>2</sub>
O
<sub>4</sub>
(M = Al, Cr, Mn, Fe and Co) crystallizing with spinel-type structure has been evaluated according to the H
<sub>2</sub>
-evolution. The oxides are black and displayed a semiconducting behavior where the electronic balance comes from a small over stochiometry (CuCo
<sub>2</sub>
O
<sub>4.016</sub>
). Electron hopping occurs between similar sites in normal spinel with a low activation energy whereas larger energies were found in inverse spinel. The electrodes were characterized photoelectrochemically and acquired the characteristic of p-type semiconductors. The conduction band edge, determined from intensity-potential curves, is located below the H
<sub>2</sub>
O/H
<sub>2</sub>
potential leading to a thermodynamically favorable H
<sub>2</sub>
-liberation under visible light. The photoactivity was dependent on preparative conditions and the best results were obtained over CuCo
<sub>2</sub>
O
<sub>4</sub>
prepared through nitrate route in presence of SO
<sup>2-</sup>
<sub>3</sub>
(3.6mlh
<sup>-1</sup>
g
<sup>-1</sup>
). Improved photoactivity may be interpreted in terms of flat band potential and electronegativity. The presence of cobalt contributes to increase the electron affinity, a desirable property for p-type specimen. It has been observed that the amount of evolved H
<sub>2</sub>
rose using stronger reductors by increasing the band bending. The initial performance of catalyst was almost restored using a fresh reactant solution. With time, the water reduction slowed down because the end products S
<sup>2-</sup>
<sub>n</sub>
and S
<sub>2</sub>
O
<sup>2-</sup>
<sub>6</sub>
compete with the adsorbed water for the photoelectrons.</div>
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<name sortKey="Saadi, S" sort="Saadi, S" uniqKey="Saadi S" first="S." last="Saadi">S. Saadi</name>
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