Synergistic CoX@g-C <sub>3</sub> N <sub>4</sub> (X = S, Se) Heterostructures for Enhanced Charge Transfer in Solar Hydrogen Production and Environmental Remediation

High Resolution Image Download MS PowerPoint Slide Heterostructure materials have gained importance as efficient semiconductor-based photocatalysts for hydrogen evolution by water splitting. We have successfully synthesized CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 chalcogenide-based heterostructures and characterized them using PXRD, UV-DRS, Raman spectra, XPS, PL, FE-SEM, HR-TEM, BET, photocurrent, and LSV. The photocatalytic water splitting efficiency was measured in DI water using TEOA as a sacrificial reagent under visible light (λ ≥ 420 nm). The H 2 evolution rates in DI water for CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 3222.34 and 2697.37 μmol g –1 h –1 with apparent quantum efficiencies (AQE) of 11.10% and 9.29%, respectively. Also, the degradation of methylene blue (MB) dye was examined here, and the efficiencies of CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were determined to be 96% and 93% under sunlight, respectively. The photocurrent densities of CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 2.28 and 1.55 mA/cm 2, respectively. The CoSe@g-C 3 N 4 sample exhibited the highest H 2 evolution, MB dye degradation, and photocurrent rate due to the greater interfacial interactions between the CoSe nanoplate and porous g-C 3 N 4 nanosheet when compared to CoS@g-C 3 N 4 . Thus, it has the high capacity to separate photogenerated charges efficiently and transfer them from g-C 3 N 4 to CoSe active sites, which helped to enhance the photocatalytic activity. The Tafel slope values for CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 51 and 66 mV dec –1, respectively. The lowest Tafel slope value of CoSe@g-C 3 N 4 exhibited a faster rate of reaction. Thus, the surface interaction between the CoSe and g-C 3 N 4 may create synergistic effects, which facilitate electron transport at the interface and significantly boost the catalytic activity. Therefore, CoSe@g-C 3 N 4 is a promising chalcogenide photocatalyst toward sustainable energy production and environmental remediation.

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Journal
ACS Sustainable Resource Management
Published
2026-06-29
DOI
https://doi.org/10.1021/acssusresmgt.6c00005
Primary Topic
Advanced Photocatalysis Techniques
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article
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article

Synergistic CoX@g-C 3 N 4 (X = S, Se) Heterostructures for Enhanced Charge Transfer in Solar Hydrogen Production and Environmental Remediation

J. Manjanna, Paresh L. Dhepe, Girish Praveen Nayaka, Raju S. Kangutkar et al.
ACS Sustainable Resource Management
Advanced Photocatalysis Techniques
article

Synergistic CoX@g-C 3 N 4 (X = S, Se) Heterostructures for Enhanced Charge Transfer in Solar Hydrogen Production and Environmental Remediation

J. Manjanna, Paresh L. Dhepe, Girish Praveen Nayaka, Raju S. Kangutkar, Mallikarjun Hanjyanatti, Priyanka Walko
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Heterostructure materials have gained importance as efficient semiconductor-based photocatalysts for hydrogen evolution by water splitting. We have successfully synthesized CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 chalcogenide-based heterostructures and characterized them using PXRD, UV-DRS, Raman spectra, XPS, PL, FE-SEM, HR-TEM, BET, photocurrent, and LSV. The photocatalytic water splitting efficiency was measured in DI water using TEOA as a sacrificial reagent under visible light (λ ≥ 420 nm). The H 2 evolution rates in DI water for CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 3222.34 and 2697.37 μmol g –1 h –1 with apparent quantum efficiencies (AQE) of 11.10% and 9.29%, respectively. Also, the degradation of methylene blue (MB) dye was examined here, and the efficiencies of CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were determined to be 96% and 93% under sunlight, respectively. The photocurrent densities of CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 2.28 and 1.55 mA/cm 2, respectively. The CoSe@g-C 3 N 4 sample exhibited the highest H 2 evolution, MB dye degradation, and photocurrent rate due to the greater interfacial interactions between the CoSe nanoplate and porous g-C 3 N 4 nanosheet when compared to CoS@g-C 3 N 4 . Thus, it has the high capacity to separate photogenerated charges efficiently and transfer them from g-C 3 N 4 to CoSe active sites, which helped to enhance the photocatalytic activity. The Tafel slope values for CoSe@g-C 3 N 4 and CoS@g-C 3 N 4 were 51 and 66 mV dec –1, respectively. The lowest Tafel slope value of CoSe@g-C 3 N 4 exhibited a faster rate of reaction. Thus, the surface interaction between the CoSe and g-C 3 N 4 may create synergistic effects, which facilitate electron transport at the interface and significantly boost the catalytic activity. Therefore, CoSe@g-C 3 N 4 is a promising chalcogenide photocatalyst toward sustainable energy production and environmental remediation.

ACS Sustainable Resource Management
National Chemical Laboratory (IN), Institute of Catalysis and Petrochemistry (RU), Indian Institute of Science Bangalore (IN)
Openalex Percentile: Top 20%
Advanced Photocatalysis Techniques
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