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Photocatalytic hydrogen production on the hetero-junction CuO/ZnO

Authors :
Mohamed Trari
Meriem Haddad
Akila Belhadi
L. Boudjellal
Source :
International Journal of Hydrogen Energy. 46:37556-37563
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

The co-precipitation is successfully used for the synthesis of the hetero-junction CuO/ZnO. Thermal analysis, ATR spectroscopy and diffuse reflectance were used to assess the photoactivity of the hetero-system for the hydrogen formation upon visible light. As expected, the X-ray diffraction shows mixed phases of CuO (tenorite) and ZnO (Wurtzite). The specific surface area is around ~7 m2 g−1 with a crystallite size lying between 20 and 49 nm. The diffuse reflectance indicates an indirect transition at 3.13 eV for ZnO and a direct transition at 1.60 eV for the sensitizer CuO. The capacitance-potential (C−2 - E) characteristic of CuO plotted in Na2SO4 electrolyte exhibits p-type comportment with a flat band potential of −0.315 VRHE and a holes concentration of 8.7 × 1018cm−3. The Electrochemical Impedance Spectroscopy exhibits a semicircle characteristic of the bulk material with an impedance of 1725 Ω cm2 which decreases down to 453 Ω cm2 under irradiation, supporting the semiconducting character of CuO. ZnO mediates the electrons transport thanks to its conduction band, formed from Zn2+: 4s orbital (−0.92 VRHE); it is positioned cathodically with respect to the H2O/H2 level (~-0.74 VRHE), producing a H2 evolution under visible light illumination. The performance peaks at pH ~7 on 5% CuO/ZnO for a catalyst dose of 0.25 mg of catalyst/mL of solution in the presence of SO32− as holes scavenger. A liberation rate of 340 μmol h−1 (g of catalyst)−1 is obtained with a quantum efficiency of 0.38% under a photons flux of 2.09 × 1019 s−1.

Details

ISSN :
03603199
Volume :
46
Database :
OpenAIRE
Journal :
International Journal of Hydrogen Energy
Accession number :
edsair.doi...........ab3096213cab71f8346f74cabaf74582
Full Text :
https://doi.org/10.1016/j.ijhydene.2020.11.053