Photoelectrochemical H2-generation over Spinel FeCr2O4 in X2- solutions (X2-Â =Â S2- and )
A. Boudjemaa,
R. Bouarab,
S. Saadi,
A. Bouguelia and
M. Trari
Applied Energy, 2009, vol. 86, issue 7-8, 1080-1086
Abstract:
Photocatalytic H2-production has been observed over FeCr2O4, synthesized from Cr(NO3)3 and Fe(NO3)3. The oxide crystallizes in the normal spinel structure and the transport properties exhibit p-type conductivity ascribed to metal deficiency. An optical gap of 1.33 eV is determined from the reflectance diffuse spectrum. From photoelectrochemical measurements, a flat band potential of +0.23 VSCE is found. The valence band, made up of cationic 3d orbital, is located at 5.2 eV (0.45 VSCE) below vacuum. Hence, the conduction band (-0.98 VSCE) allows a thermodynamically feasible H2 liberation under visible light. In aqueous electrolytes, the oxide is stabilized by hole consumption involving X2- species and the best photoactivity for H2-production is obtained in S2- solution with an evolution rate of 8.26 cm3 g-1 h-1. The tendency towards saturation is due to the competitive reduction of the end products namely and with water and to the yellow color of . On the other hand and for a comparative purpose, the catalytic activity of unreduced FeCr2O4 for the water-gas shift reaction (CO + H2O --> CO2 + H2) is studied in the temperature range 523-723 K. At 723 K, the rate of H2-formation and the degree of CO conversion are respectively 280 [mu]mol g-1 s-1 and 44%.
Keywords: Hydrogen; Spinel; Photoelectrochemical; Water-gas; shift (search for similar items in EconPapers)
Date: 2009
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