Highly efficient degradation of Ponceau S using a solar-light-driven Z-scheme ZnMn2O4/ZnO heterojunction photocatalyst

A ZnMn 2 O 4 /ZnO heterojunction was prepared via a solid dispersion method for the photocatalytic degradation of Ponceau S (PS) under solar irradiation. The structural, textural, morphological, optical, and electrochemical properties of the synthesized materials were systematically characterized. UV–Vis DRS revealed band gap energies of 1.92 eV for ZnMn 2 O 4 and 3.14 eV for ZnO, supporting the formation of a direct Z -scheme heterojunction, which promotes efficient charge separation. The ZnMn 2 O 4 /ZnO heterostructure exhibited superior photocatalytic performance compared to the individual components, achieving 97.21% degradation efficiency under optimized conditions (photocatalyst dosage: 0.3 g/L; PS concentration: 15 mg/L; reaction time: 180 min and pH: 5.9) with a short half-life of 39.72 min. The low relative standard deviation (RSD = 0.25%) confirms the excellent reproducibility of the results. Scavenger experiments identified O 2 •- and h + as the dominant reactive species. The heterojunction retained a removal efficiency of 79.91% after six cycles, demonstrating good stability without significant structural deterioration. Monte Carlo and molecular dynamics simulations revealed strong interactions and high adsorption affinity of PS on the ZnMn 2 O 4 /ZnO surface. Furthermore, toxicity analysis confirmed that the degradation byproducts exhibit lower acute toxicity than the parent dye.

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Journal
Journal of Water Process Engineering
Published
2026-06-12
DOI
https://doi.org/10.1016/j.jwpe.2026.110327
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Highly efficient degradation of Ponceau S using a solar-light-driven Z-scheme ZnMn2O4/ZnO heterojunction photocatalyst

P. Haraux, D. Horwat, N. Ahmia, M. Benamira et al.
Journal of Water Process Engineering
Advanced Photocatalysis Techniques
article

Highly efficient degradation of Ponceau S using a solar-light-driven Z-scheme ZnMn2O4/ZnO heterojunction photocatalyst

P. Haraux, D. Horwat, N. Ahmia, M. Benamira, S. Bruyère, L. Messaadia
article en

Abstract

A ZnMn 2 O 4 /ZnO heterojunction was prepared via a solid dispersion method for the photocatalytic degradation of Ponceau S (PS) under solar irradiation. The structural, textural, morphological, optical, and electrochemical properties of the synthesized materials were systematically characterized. UV–Vis DRS revealed band gap energies of 1.92 eV for ZnMn 2 O 4 and 3.14 eV for ZnO, supporting the formation of a direct Z -scheme heterojunction, which promotes efficient charge separation. The ZnMn 2 O 4 /ZnO heterostructure exhibited superior photocatalytic performance compared to the individual components, achieving 97.21% degradation efficiency under optimized conditions (photocatalyst dosage: 0.3 g/L; PS concentration: 15 mg/L; reaction time: 180 min and pH: 5.9) with a short half-life of 39.72 min. The low relative standard deviation (RSD = 0.25%) confirms the excellent reproducibility of the results. Scavenger experiments identified O 2 •- and h + as the dominant reactive species. The heterojunction retained a removal efficiency of 79.91% after six cycles, demonstrating good stability without significant structural deterioration. Monte Carlo and molecular dynamics simulations revealed strong interactions and high adsorption affinity of PS on the ZnMn 2 O 4 /ZnO surface. Furthermore, toxicity analysis confirmed that the degradation byproducts exhibit lower acute toxicity than the parent dye.

Journal of Water Process EngineeringVol. 90
University of Jijel (DZ), Centre National de la Recherche Scientifique (FR), Institut Jean Lamour (FR)
Agence Thématique de Recherche en Science et Technologie
Openalex Percentile: Top 18%
Advanced Photocatalysis Techniques
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Highly efficient degradation of Ponceau S using a solar-light-driven Z-scheme ZnMn2O4/ZnO heterojunction photocatalyst — P. Haraux, D. Horwat, et al. · Journal of Water Process Engineering (2026) | TGRS Research Map | TGRS