Abstract
A simple grinding method using polyvinylpyrrolidone (PVP) as a capping agent is introduced to synthesize CoFe2O4 nanoparticles. The effects of calcination temperature (ranging from 450 to 850 °C) on the structural, morphological, physical, and optical properties of the materials are investigated using various techniques, including thermogravimetric analysis/differential scanning calorimetry (TGA/DSC), powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), N2 adsorption isotherm, ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), and vibrating sample magnetometry (VSM). The presence of PVP significantly suppresses the agglomeration of the materials, resulting in a nanocrystalline size of 18 nm for a sample calcined at 650 °C, which is approximately 38% smaller than that of the sample synthesized without PVP. Among the materials studied, the sample calcined at 650 °C exhibits unique properties, including optimal average pore size, specific surface area, and band gap energy, contributing to its superior photocatalytic degradation of rhodamine B via the Fenton reaction. Systematic experiments are performed to investigate the effects of pH, catalyst dosage, dye, and H2O2 concentrations and competitive anions on the rhodamine B degradation. Additionally, the Fenton photodegradation of RhB on CoFe2O4 is well-fitted to the first-order kinetic model. The redox pairs of Co(III)/Co(II) and Fe(III)/Fe(II) in the CoFe2O4 spinel structure might facilitate the formation of Fenton radicals, contributing to the decomposition of RhB through a proposed four-step mechanism. Notably, the material exhibits a strong magnetic response and maintains its excellent performance over five cycles, demonstrating the high potential for reusability as a photocatalyst.
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