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Nowadays, water pollution generated from textile effluents is one of the major problems for the human race and ecology. Hence, development of sustainable strategies to lower the water pollution level has become a burning need. In this regard, the present study focuses on the preparation of nano catalyst NiFeO to catalyze the chemical reactions on industrial organic dyes for their fast cleansing from water. By sol-gel auto-combustion technique, NiFeO nanoparticles were synthesized and exposed to thermal process at temperatures of 400, 600, and 800 °C. Highly crystalline phase with spinel cubic structured NiFeO was formed with a crystal size of 18.71 nm, which was confirmed by XRD analysis. The FTIR spectra showed two fundamental absorption bands in the range 597.80-412.59 cm, which are the characteristics of tetrahedral M - O and octahedral M - O bond in NiFeO. The surface morphology of calcined NiFeO was investigated by scanning electron microscope (SEM). The nanoparticle size analyzer exhibited that the synthesized NiFeO nanoparticles had an average particle size of ∼ 291.3 nm. Three stage decomposition patterns were observed for NiFeO, which was analyzed by a temperature programmed STA. Zeta potential analyzer showed that the synthesized sample S1 and S2 were stable in the dispersion medium. Also, NiFeO exhibited optical band gap energies for direct band transitions within the visible spectrum measured to be 1.43-1.45 eV, rendering them effective as photocatalysts under sunlight. The samples showed magnetic measurements by VSM with saturation magnetization, coercivity, remnant magnetization value of 66.81 emu/g, 4.13 Oe and 12.94 emu/g, respectively. The synthesized photocatalyst, NiFeO, at 400 °C, significantly degraded three toxic organic pollutants-Methylene blue, Rhodamine B, and Congo Red-under visible light through 'Photo-Fenton' reaction mechanisms. Among the three dyes, Methylene Blue exhibited the highest degradation percentage with a rate constant of 0.0149 min and followed pseudo-first-order kinetic model.
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http://dx.doi.org/10.1016/j.heliyon.2024.e37199 | DOI Listing |
Energy Fuels
August 2025
Group of Energy Materials, École polytechnique fédérale de Lausanne (EPFL), Rue de l'Industrie 17, Sion, Valais 1951, Switzerland.
Anion exchange membrane water electrolyzers (AEMWEs) offer a promising alternative to proton exchange membrane (PEM) electrolyzers, leveraging non-precious-metal catalysts and alkaline electrolytes for cost reduction. However, challenges persist in achieving long-term durability, high current densities, and stable membrane performance. While previous studies have examined AEM development, a comprehensive structural-electrochemical analysis of AEMWE components under prolonged operation remains limited.
View Article and Find Full Text PDFMicromachines (Basel)
July 2025
Key Laboratory of Low-Dimensional Structural Physics and Application, Education Department of Guangxi Zhuang Autonomous Region, College of Physics and Electronic Information Engineering, Guilin University of Technology, Guilin 541004, China.
Despite significant progress in photoelectrochemical (PEC) water splitting, high fabrication costs and limited efficiency of photoanodes hinder practical applications. Bismuth vanadate (BiVO), with its low cost, non-toxicity, and suitable band structure, is a promising photoanode material but suffers from poor charge transport, sluggish surface kinetics, and photocorrosion. In this study, porous monoclinic BiVO films are fabricated via a simplified successive ionic layer adsorption and reaction (SILAR) method, followed by borate treatment and PEC deposition of NiFeO.
View Article and Find Full Text PDFMolecules
August 2025
Department of Chemical Engineering, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Anion exchange membrane (AEM) water electrolysis is a potentially inexpensive and efficient source of hydrogen production as it uses effective low-cost catalysts. The catalytic activity and performance of nickel iron oxide (NiFeO) catalysts for hydrogen production in AEM water electrolyzers were investigated. The NiFeO catalysts were synthesized with various iron content weight percentages, and at the stoichiometric ratio for nickel ferrite (NiFeO).
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, 212013, China.
The replacement of the anodic OER for water splitting with the UOR is a promising pathway for energy-efficient hydrogen production and treatment of urea-containing wastewater. In this work, we report a new partially sulfurized nickel-iron oxide catalyst (S-NiFeO/NF) containing oxygen vacancies on nickel foam by constructing M-S bonds with spinel compounds as substrates. S-NiFeO/NF demonstrated very favourable UOR and HER activities as well as stability.
View Article and Find Full Text PDFJACS Au
June 2025
School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, P. R. China.
Operando examination of reaction intermediates during (photo)-electrocatalytic processes, particularly with respect to their kinetics, is a critical but challenging task. Spectroelectrochemical (SEC) methods based on UV-vis spectroscopy offer potential insights into intermediate species, although they are often applied under steady-state conditions. In this work, we employ excitation-modulated absorption spectroscopy (EMAS), which utilizes periodic modulation of either potential or light intensity, to dynamically probe the SEC responses of a hematite (FeO) photoanode, NiFeO -type electrocatalysts, and their composites.
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