Structure tunning of MoS2@Fe3O4 by modulating electron density for enhanced Fenton-like PMS activation: Accelerated Fe (III)/Fe (II) cycle for efficient micropollutants removal

1T-MoS 2 is a promising material for regulating the electronic structure of Fe-based catalyst to enhance PMS activation, due to the higher chemical reactivity of the basal plane with excellent intrinsic electronic properties. Herein, an excellent MoS 2 @Fe 3 O 4 by using 1T- MoS 2 as support to tune electronic structure, labeling as 1T-MoS 2 @Fe 3 O 4 , was successfully synthesized for faster and enhanced micropollutants degradation via Fenton-like peroxomonosulfate (PMS) activation. The composite showed remarkable catalytic performance, as evidenced by a removal rate of 1.12 × 10 −1 min −1 for caffeine, which was 4.50 times higher than that of 2H-MoS 2 @Fe 3 O 4 , attributed to the robust capacity for Fe (II) regeneration. The efficiency of the 1T-MoS 2 @Fe 3 O 4 /PMS system was affected by pH, PMS and catalyst dosages, as well as water chemistry. Additionally, the potential mechanism for PMS activation was explored, showing that O 2 • were the dominant reactive oxygen species (ROS) generated in the system due to the electron-rich O sites on the composite, and electron transfer processes play an important role during PMS activation. The Mo (IV) active sites facilitated accelerated Fe (III)/Fe (II) cycle, which promoted the rapid PMS activation. Excellent degradation of micropollutants (MPs) mixture in real secondary effluent was achieved by 1T-MoS 2 @Fe 3 O 4 /PMS system. The possible degradation pathways of caffeine (CAF), ibuprofen (IBP), and carbamazepine (CBZ) were also investigated. This study offers a new perspective on MoS 2 as a co-catalyst/support within Fenton-like system. • 1T-MoS 2 prevented the Fe 3 O 4 aggregation and tuned the electronic structure of the composite. • Excellent catalytic performance of the composite is attributed to Fe (III) lower electron density and abundant e – of 1T-MoS 2 . • Mo (IV) active sites in eletron-abundant 1T-MoS 2 promoted and expedited Fe (II) regeneration. • Both reactive oxygen species and electron transfer processes participated in CAF degradation.

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Publication Details

Journal
Journal of environmental chemical engineering
Published
2024-11-26
DOI
https://doi.org/10.1016/j.jece.2024.114944
Citations
14
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
1.43
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article

Structure tunning of MoS2@Fe3O4 by modulating electron density for enhanced Fenton-like PMS activation: Accelerated Fe (III)/Fe (II) cycle for efficient micropollutants removal

Mohamed Gamal El‐Din, Ziang Chang, Qi Feng, Soliu Oladejo Ganiyu
14 citations
Journal of environmental chemical engineering
Advanced Photocatalysis Techniques
1.43
article

Structure tunning of MoS2@Fe3O4 by modulating electron density for enhanced Fenton-like PMS activation: Accelerated Fe (III)/Fe (II) cycle for efficient micropollutants removal

Mohamed Gamal El‐Din, Ziang Chang, Qi Feng, Soliu Oladejo Ganiyu
article en
14 citations

Abstract

1T-MoS 2 is a promising material for regulating the electronic structure of Fe-based catalyst to enhance PMS activation, due to the higher chemical reactivity of the basal plane with excellent intrinsic electronic properties. Herein, an excellent MoS 2 @Fe 3 O 4 by using 1T- MoS 2 as support to tune electronic structure, labeling as 1T-MoS 2 @Fe 3 O 4 , was successfully synthesized for faster and enhanced micropollutants degradation via Fenton-like peroxomonosulfate (PMS) activation. The composite showed remarkable catalytic performance, as evidenced by a removal rate of 1.12 × 10 −1 min −1 for caffeine, which was 4.50 times higher than that of 2H-MoS 2 @Fe 3 O 4 , attributed to the robust capacity for Fe (II) regeneration. The efficiency of the 1T-MoS 2 @Fe 3 O 4 /PMS system was affected by pH, PMS and catalyst dosages, as well as water chemistry. Additionally, the potential mechanism for PMS activation was explored, showing that O 2 • were the dominant reactive oxygen species (ROS) generated in the system due to the electron-rich O sites on the composite, and electron transfer processes play an important role during PMS activation. The Mo (IV) active sites facilitated accelerated Fe (III)/Fe (II) cycle, which promoted the rapid PMS activation. Excellent degradation of micropollutants (MPs) mixture in real secondary effluent was achieved by 1T-MoS 2 @Fe 3 O 4 /PMS system. The possible degradation pathways of caffeine (CAF), ibuprofen (IBP), and carbamazepine (CBZ) were also investigated. This study offers a new perspective on MoS 2 as a co-catalyst/support within Fenton-like system. • 1T-MoS 2 prevented the Fe 3 O 4 aggregation and tuned the electronic structure of the composite. • Excellent catalytic performance of the composite is attributed to Fe (III) lower electron density and abundant e – of 1T-MoS 2 . • Mo (IV) active sites in eletron-abundant 1T-MoS 2 promoted and expedited Fe (II) regeneration. • Both reactive oxygen species and electron transfer processes participated in CAF degradation.

Journal of environmental chemical engineeringVol. 12(6)
University of Alberta (CA), Chongqing University (CN)
Affordable and clean energy
Openalex Percentile: Top 19%
Advanced Photocatalysis Techniques
1.43
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