Peroxymonosulfate (PMS) heterogeneous catalysis dominated by nonradical pathway showed excellent adaptability for pollutant removal in complex water matrixes. Herein, ultra-small Fe-doped MoS nanosheets with N-doped carbon intercalation (CF-MoS) were synthesized via a one-step hydrothermal method to treat high salinity organic wastewater. CF-MoS exhibited an expanded interlayer spacing by 1.63 times and the specific surface area by 9 times compared with Fe-doped MoS (F-MoS), substantially increasing the active sites. Homogeneous Fe catalytic experiments confirmed that the promotion of carbon intercalated MoS (C-MoS) on Fe/Fe redox cycle was much higher than pure MoS. Besides, the considerable removal of tetracycline (TC) under high salinity conditions (0-7.1%) was attributed to the dominant role of PMS nonradical oxidation pathways, including O and surface-bound radicals. The catalytic sites included Fe/Fe, Mo/Mo/Mo, C=O, pyridine N, pyrrolic N and hydroxyl groups. Finally, density functional theory (DFT) was employed to get the radical electrophilic attack sites and nucleophile attack sites of TC, and the results were consistent with the TC degradation products determined by HPLC-MS. This work would broaden the application of MoS-based catalysts, especially for PMS catalytic removal of organic pollutants from high salinity wastewater.
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http://dx.doi.org/10.1016/j.jcis.2022.07.145 | DOI Listing |
Nano Lett
October 2024
The Institute for Advanced Studies, Wuhan University, Wuhan 430072, China.
Front Chem
May 2024
Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Chhatrapati Sambhajinagar, Maharashtra, India.
This review provides a comprehensive overview of the production and modification of CZTS nanoparticles (NPs) and their application in electrocatalysis for water splitting. Various aspects, including surface modification, heterostructure design with carbon nanostructured materials, and tunable electrocatalytic studies, are discussed. A key focus is the synthesis of small CZTS nanoparticles with tunable reactivity, emphasizing the sonochemical method's role in their formation.
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December 2024
Electric Mobility and Tribology Research Group (EM&TRG), Council of Scientific and Industrial Research-Central Mechanical Engineering Research Institute, Durgapur, 713209, India.
Herein, a self-supported, robust, and noble-metal-free 3D hierarchical interface-rich Fe-doped Co-LDH@MoS-NiS/NF heterostructure electrocatalyst has been prepared through a controllable two-step hydrothermal process. The resultant electrode shows low overpotential of ~95 mV for hydrogen evolution reaction (HER), ~220 mV for the oxygen evolution reaction (OER), and the two-electrode system requires only a cell voltage of ~1.54 V at 10 mA cm current density, respectively.
View Article and Find Full Text PDFDalton Trans
December 2023
School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, Anhui, 230009, PR China.
Heterostructures formed by combining semiconductor materials with different band structures can provide work functions, d-band positions and electronic properties different from bulk materials and are considered as an effective strategy to improve the catalytic activity through electronic modification. In this study, an efficient MoS/Fe-NiS/NF heterojunction material was prepared by a two-step hydrothermal method. With the help of flake Ni(OH) synthesized in the first step, growth sites were provided for flake NiS.
View Article and Find Full Text PDFDalton Trans
October 2023
College of Mechanical and Electrical Engineering, Qingdao University, Qingdao 266071, China.
To replace the current expensive precious metal catalysts for water electrolysis, it is important to develop inexpensive and powerful bifunctional catalysts for hydrogen production. It is an effective way to improve catalytic performance using excellent templates and elemental doping. Here, a hierarchical structure Fe-CoS/MoS was synthesized using an Fe-ZIF precursor prepared by ion exchange, followed by hydrothermal sulfuration and annealing.
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