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Preparation of Mn3O4 nanoparticles on Al-substrate for degradation of Rhodamine B under solar light

  • A. Chaa,
  • A. Haddad,
  • G. Rekhila,
  • S. Tria,
  • M. Trari

摘要

The semiconducting properties of Mn3O4 thin films were assessed for the heterogeneous photocatalytic oxidation of Rhodamine B (Rh B). The films were grown on Al-substrate using a spray coating, and their physical and photoelectrochemical characteristics were studied. X-ray diffraction analysis showed a well-crystallized structure of the spinel Mn3O4. The atomic force microscopy revealed dense and irregular grains with a mean size of ~ 50 nm and a thickness of ~ 1 µm. The direct optical transition at 2.19 eV, in agreement with the brown color, is assigned to d–d transitions within the incomplete Mn-3d shell, which enables efficient photocatalytic conversion of the solar radiation. The photoelectrochemical measurements demonstrated p-type comportment, evidenced by a negative slope in the [capacitance−2–potential: C−2–E] graph with a flat band potential of + 0.35 VSCE and a hole density of 6.5 × 1018 cm−3. The electrochemical impedance spectroscopy (EIS) plot showed a semicircle due to a capacitive comportment of the bulk spinel (Rb = 70 kΩ cm2). The center positioned below the abscissa axis (− 23°) with a constant phase element (CPE). The conduction band (− 1.64 VSCE) is more cathodic than the \({\text{O}}_{{2}} /{\text{O}}_{{2}}^{ \bullet - }\) O 2 / O 2 - level, thus catalyzing the photocatalytic process by \({\text{O}}_{{2}}^{ \bullet - }\) O 2 - radicals. Under sunlight, 50% reduction of the Rh B concentration (10 ppm) was achieved within 1 h, the color removal, followed by spectrophotometry obeys a pseudo-first-order kinetic model with a rate constant of 9.9 × 10–3 min−1 (t1/2 = 70 min).