<p>The photoreduction of environmental contaminants such as nitrate (NO<sub>3</sub><sup>−</sup>) and carbon dioxide (CO<sub>2</sub>) into clean and renewable fuels has emerged as a key strategy for mitigating global environmental challenges, in which perovskite photocatalysts offer a promising, cost-effective, and sustainable solution. In the current research, a novel CuBi<sub>2</sub>S<sub>4</sub>/Al<sub>2</sub>WO<sub>6</sub>/Ti<sub>3</sub>C<sub>2</sub> MXene Schottky/Z-scheme ternary heterojunction photocatalyst was synthesized and developed for the efficient photoreduction of nitrate and carbon dioxide, as well as photocatalytic water splitting under visible-light irradiation. The nanocomposite integrates three distinct components: (i) zero-dimensional (0D) CuBi<sub>2</sub>S<sub>4</sub> quantum dot (QDs) nanoparticles (acting as a metal-assisted sulfide perovskite photocatalyst), (ii) three-dimensional (3D) aluminum tungstate (Al<sub>2</sub>WO<sub>6</sub>) double perovskite (serving as the central oxide perovskite photocatalyst), and (iii) two-dimensional (2D) Ti<sub>3</sub>C<sub>2</sub> MXene (functioning as a non-metallic co-catalyst facilitating interfacial charge transfer). A comprehensive assessment of operating factors revealed their significant influence on the photocatalytic behavior of the CuBi<sub>2</sub>S<sub>4</sub>/Al<sub>2</sub>WO<sub>6</sub>/Ti<sub>3</sub>C<sub>2</sub> ternary photocatalyst. The CuBi<sub>2</sub>S<sub>4</sub>/Al<sub>2</sub>WO<sub>6</sub>/Ti<sub>3</sub>C<sub>2</sub> photocatalyst achieved a nitrate reduction efficiency of 80%, with nitrogen gas (N<sub>2</sub>) identified as the predominant reduction product (55% selectivity). The same catalyst also exhibited a CO<sub>2</sub> photoreduction efficiency of 70%, in which methane (CH<sub>4</sub>) displayed the highest generation rate (13.87 mL·g<sup>−1</sup>·h<sup>−</sup>1; 619 µmol·g<sup>−1</sup>·h<sup>−1</sup>) corresponding to a 50% selectivity. Moreover, the composite demonstrated an impressive hydrogen evolution rate of 16 mL·g<sup>−1</sup>·h<sup>−1</sup> (714 µmol·g<sup>−1</sup>·h<sup>−1</sup>) during photocatalytic water splitting with an efficiency of 60%. Furthermore, the ternary heterojunction photocatalyst exhibited excellent reusability and structural stability, retaining its photocatalytic performance over five consecutive cycles.</p>

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Highly efficient visible-light-driven photoreduction of nitrate, carbon dioxide, and water by a CuBi2S4/Al2WO6/Ti3C2 MXene Schottky/Z-scheme ternary photocatalyst

  • Hossein Kadkhodayan,
  • Taher Alizadeh

摘要

The photoreduction of environmental contaminants such as nitrate (NO3) and carbon dioxide (CO2) into clean and renewable fuels has emerged as a key strategy for mitigating global environmental challenges, in which perovskite photocatalysts offer a promising, cost-effective, and sustainable solution. In the current research, a novel CuBi2S4/Al2WO6/Ti3C2 MXene Schottky/Z-scheme ternary heterojunction photocatalyst was synthesized and developed for the efficient photoreduction of nitrate and carbon dioxide, as well as photocatalytic water splitting under visible-light irradiation. The nanocomposite integrates three distinct components: (i) zero-dimensional (0D) CuBi2S4 quantum dot (QDs) nanoparticles (acting as a metal-assisted sulfide perovskite photocatalyst), (ii) three-dimensional (3D) aluminum tungstate (Al2WO6) double perovskite (serving as the central oxide perovskite photocatalyst), and (iii) two-dimensional (2D) Ti3C2 MXene (functioning as a non-metallic co-catalyst facilitating interfacial charge transfer). A comprehensive assessment of operating factors revealed their significant influence on the photocatalytic behavior of the CuBi2S4/Al2WO6/Ti3C2 ternary photocatalyst. The CuBi2S4/Al2WO6/Ti3C2 photocatalyst achieved a nitrate reduction efficiency of 80%, with nitrogen gas (N2) identified as the predominant reduction product (55% selectivity). The same catalyst also exhibited a CO2 photoreduction efficiency of 70%, in which methane (CH4) displayed the highest generation rate (13.87 mL·g−1·h1; 619 µmol·g−1·h−1) corresponding to a 50% selectivity. Moreover, the composite demonstrated an impressive hydrogen evolution rate of 16 mL·g−1·h−1 (714 µmol·g−1·h−1) during photocatalytic water splitting with an efficiency of 60%. Furthermore, the ternary heterojunction photocatalyst exhibited excellent reusability and structural stability, retaining its photocatalytic performance over five consecutive cycles.