<p>The present work describes the color removal of Rhodamine B (Rh B), a recalcitrant cationic dye by electrocatalysis and electro-photocatalysis on Ba<sub>2</sub>SnO<sub>4</sub> as anode. The double perovskite Ba<sub>2</sub>SnO<sub>4</sub> synthesized by nitrate route was characterized by physical and electrochemical methods, a preamble of Rh B oxidation. The single phase, confirmed by X-ray diffraction, crystallizes in a tetragonal (Space Group: I4/mmm), with spherical crystallites (~ 50&#xa0;nm). The zeta-sizer analysis gives an average grains size of 0.65&#xa0;µm and zeta-potential of − 20&#xa0;mV. The SEM analysis revealed the porosity of the oxide and the Ba–O and Sn–O bonds were confirmed by the FT-IR analysis. The direct optical gap (3.18&#xa0;eV), determined by diffuse reflectance, is assigned to the charge transfer O<sup>2−</sup>: 2<i>p</i> → Sn<sup>4+</sup>: 5<i>&#xa0;s</i>, and the double perovskite possesses a chemical inertness in the entire pH region. The Mott–Schottky plot indicates <i>n</i>-type behavior with a flat band potential (<i>E</i><sub>fb</sub>) of − 0.84 <i>V</i><sub>SCE</sub>, due to O<sup>2−</sup> deficiency and an electron concentration N<sub>D</sub> of 1.14 <InlineEquation ID="IEq1"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="13738_2025_3208_Article_IEq1.gif" Format="GIF" Height="13" Rendition="HTML" Resolution="72" Type="Linedraw" Width="19" /> </InlineMediaObject> <EquationSource Format="TEX">\(\times\)</EquationSource> <EquationSource Format="MATHML"><math> <mo>×</mo> </math></EquationSource> </InlineEquation> 10<sup>17</sup>&#xa0;cm<sup>−3</sup>. The electrochemical impedance spectroscopy (EIS), plotted at the free potential (+ 0.5&#xa0;V), reveals the bulk and grain boundaries contributions. The low electrons mobility is assigned to a narrow conduction band of Sn<sup>4+</sup>: 5<i>&#xa0;s</i> parentage with activation energy (18&#xa0;meV) in conformity with a conduction mechanism by small lattice polaron hopping. The intensity-potential <i>J</i>(<i>E</i>) profile in NaCl (10<sup>–2</sup>&#xa0;M) exhibits a small hysteresis similar to a chemical diode. The semi-logarithmic plot (log<i>J</i> – <i>E</i>) indicates a chemical stability of Ba<sub>2</sub>SnO<sub>4</sub> in the working solution (NaCl). Ba<sub>2</sub>SnO<sub>4</sub> is of interest for the environmental protection and as application, Rh B (20&#xa0;mg L<sup>−1</sup>) was successfully oxidized by electrocatalysis with an abatement of 66% under a direct current of 150&#xa0;mA, which has a bactericidal effect. An enhancement up to 92% has been reached by electro-photocatalysis; a quasi-complete discoloration occurred within 70&#xa0;min in the “<i>Electric Current-Sunlight-Ba</i><sub><i>2</i></sub><i>SnO</i><sub><i>4</i></sub>”. The Rh B elimination follows a pseudo-first-order kinetic with a rate constant of 1.96 ± 0.17 × 10<sup>–2</sup>&#xa0;min<sup>−1</sup> (<i>t</i><sub>1/2</sub> = 35&#xa0;min) and a reaction mechanism is suggested.</p>

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Efficient oxidation by electro-photocatalysis of Rhodamine B using Ba2SnO4 as photo-electrode

  • A. Sahmi,
  • H. Lahmar,
  • M. Benamira,
  • M. Trari

摘要

The present work describes the color removal of Rhodamine B (Rh B), a recalcitrant cationic dye by electrocatalysis and electro-photocatalysis on Ba2SnO4 as anode. The double perovskite Ba2SnO4 synthesized by nitrate route was characterized by physical and electrochemical methods, a preamble of Rh B oxidation. The single phase, confirmed by X-ray diffraction, crystallizes in a tetragonal (Space Group: I4/mmm), with spherical crystallites (~ 50 nm). The zeta-sizer analysis gives an average grains size of 0.65 µm and zeta-potential of − 20 mV. The SEM analysis revealed the porosity of the oxide and the Ba–O and Sn–O bonds were confirmed by the FT-IR analysis. The direct optical gap (3.18 eV), determined by diffuse reflectance, is assigned to the charge transfer O2−: 2p → Sn4+: 5 s, and the double perovskite possesses a chemical inertness in the entire pH region. The Mott–Schottky plot indicates n-type behavior with a flat band potential (Efb) of − 0.84 VSCE, due to O2− deficiency and an electron concentration ND of 1.14 \(\times\) × 1017 cm−3. The electrochemical impedance spectroscopy (EIS), plotted at the free potential (+ 0.5 V), reveals the bulk and grain boundaries contributions. The low electrons mobility is assigned to a narrow conduction band of Sn4+: 5 s parentage with activation energy (18 meV) in conformity with a conduction mechanism by small lattice polaron hopping. The intensity-potential J(E) profile in NaCl (10–2 M) exhibits a small hysteresis similar to a chemical diode. The semi-logarithmic plot (logJE) indicates a chemical stability of Ba2SnO4 in the working solution (NaCl). Ba2SnO4 is of interest for the environmental protection and as application, Rh B (20 mg L−1) was successfully oxidized by electrocatalysis with an abatement of 66% under a direct current of 150 mA, which has a bactericidal effect. An enhancement up to 92% has been reached by electro-photocatalysis; a quasi-complete discoloration occurred within 70 min in the “Electric Current-Sunlight-Ba2SnO4”. The Rh B elimination follows a pseudo-first-order kinetic with a rate constant of 1.96 ± 0.17 × 10–2 min−1 (t1/2 = 35 min) and a reaction mechanism is suggested.