Interfacial S-scheme charge transfer in MgIn <sub>2</sub> S <sub>4</sub> /ZnO heterojunction for enhanced photodegradation of tetracycline and efficient water splitting

Environmental pollution and high energy costs are among today's most pressing global challenges. Photocatalysis offers a cost-effective and environmentally sustainable strategy to address these issues by enabling efficient pollutant degradation and hydrogen production. This work constructed a nanoflower MgIn<sub>2</sub>S<sub>4</sub> and nanorod ZnO heterojunction to enhance photocatalytic performance through an interfacial S-scheme charge transfer mechanism. Unlike most reported ZnO-based heterojunctions in the literature, this approach introduces MgIn<sub>2</sub>S<sub>4</sub>, a ternary sulfide with a narrow band gap and a high conduction band potential, to form a heterostructure material with a strong redox potential and efficient charge separation. The MgIn<sub>2</sub>S<sub>4</sub>/ZnO heterojunction exhibited superior photocatalytic activity, achieving a remarkable 94% tetracycline (TCE) degradation efficiency, 1.4 and 3.9 times higher than that of pristine MgIn<sub>2</sub>S<sub>4</sub> and ZnO, respectively. Furthermore, the heterojunction demonstrated an improved hydrogen evolution rate of 8.29 mmol h<sup>-1</sup> g<sup>-1</sup>, significantly surpassing ZnO (6.96 mmol h<sup>-1</sup> g<sup>-1</sup>) and MgIn<sub>2</sub>S<sub>4</sub> (6.24 mmol h<sup>-1</sup> g<sup>-1</sup>). The enhanced performance is attributed to the efficient interfacial charge transfer, as confirmed by X-ray photoelectron spectroscopy (XPS) analysis and electrochemical characterization, demonstrating charge migration from MgIn<sub>2</sub>S<sub>4</sub> to ZnO. Mechanistic investigations further revealed that the S-scheme charge transfer mechanism effectively promoted charge separation and facilitated the generation of reactive radical species, ultimately leading to improved photocatalytic activity. This study highlights the potential of the rationally designed MgIn<sub>2</sub>S<sub>4</sub>/ZnO S-scheme heterojunction as a highly efficient and sustainable photocatalyst for organic pollutant degradation and hydrogen production under visible light irradiation, providing a promising solution to environmental and energy challenges.

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Publication Details

Journal
Nanoscale Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5na00573f
Citations
7
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
2.54

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article

Interfacial S-scheme charge transfer in MgIn 2 S 4 /ZnO heterojunction for enhanced photodegradation of tetracycline and efficient water splitting

Tunde L. Yusuf, Kwena D. Modibane, Damian Chinedu Onwudiwe, Daniel Masekela et al.
7 citations
Nanoscale Advances
Advanced Photocatalysis Techniques
2.54
article

Interfacial S-scheme charge transfer in MgIn 2 S 4 /ZnO heterojunction for enhanced photodegradation of tetracycline and efficient water splitting

Tunde L. Yusuf, Kwena D. Modibane, Damian Chinedu Onwudiwe, Daniel Masekela, Oluwaseyi D. Saliu, Olalekan C. Olatunde
article en
7 citations

Abstract

Environmental pollution and high energy costs are among today's most pressing global challenges. Photocatalysis offers a cost-effective and environmentally sustainable strategy to address these issues by enabling efficient pollutant degradation and hydrogen production. This work constructed a nanoflower MgIn<sub>2</sub>S<sub>4</sub> and nanorod ZnO heterojunction to enhance photocatalytic performance through an interfacial S-scheme charge transfer mechanism. Unlike most reported ZnO-based heterojunctions in the literature, this approach introduces MgIn<sub>2</sub>S<sub>4</sub>, a ternary sulfide with a narrow band gap and a high conduction band potential, to form a heterostructure material with a strong redox potential and efficient charge separation. The MgIn<sub>2</sub>S<sub>4</sub>/ZnO heterojunction exhibited superior photocatalytic activity, achieving a remarkable 94% tetracycline (TCE) degradation efficiency, 1.4 and 3.9 times higher than that of pristine MgIn<sub>2</sub>S<sub>4</sub> and ZnO, respectively. Furthermore, the heterojunction demonstrated an improved hydrogen evolution rate of 8.29 mmol h<sup>-1</sup> g<sup>-1</sup>, significantly surpassing ZnO (6.96 mmol h<sup>-1</sup> g<sup>-1</sup>) and MgIn<sub>2</sub>S<sub>4</sub> (6.24 mmol h<sup>-1</sup> g<sup>-1</sup>). The enhanced performance is attributed to the efficient interfacial charge transfer, as confirmed by X-ray photoelectron spectroscopy (XPS) analysis and electrochemical characterization, demonstrating charge migration from MgIn<sub>2</sub>S<sub>4</sub> to ZnO. Mechanistic investigations further revealed that the S-scheme charge transfer mechanism effectively promoted charge separation and facilitated the generation of reactive radical species, ultimately leading to improved photocatalytic activity. This study highlights the potential of the rationally designed MgIn<sub>2</sub>S<sub>4</sub>/ZnO S-scheme heterojunction as a highly efficient and sustainable photocatalyst for organic pollutant degradation and hydrogen production under visible light irradiation, providing a promising solution to environmental and energy challenges.

Nanoscale AdvancesVol. 7(16)
University of Ilorin (NG), North-West University (ZA), University of Illinois Chicago (US), University of Pretoria (ZA), University of Limpopo (ZA)
Royal Society of Chemistry, University of Pretoria
Openalex Percentile: Top 10%
Advanced Photocatalysis Techniques
2.54
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