Cu/Zn Co-doped MgO nanoparticles with tailored structural, optical, magnetic, and photocatalytic properties for electronic and environmental applications
摘要
Nanostructured metal oxides have become integral to the advancement of functional materials for modern electronic, optoelectronic, and environmental technologies. Magnesium oxide (MgO), a wide-bandgap ceramic, is particularly attractive due to its thermal stability, defect-engineered electronic behavior, and surface reactivity. However, its limited photocatalytic and magnetic properties hinder broader applicability in multifunctional systems. In this work, Cu and Zn co-doped MgO nanoparticles were synthesized via a simple co-precipitation route and comprehensively characterized to assess their potential as multifunctional materials. XRD confirmed the formation of a cubic MgO phase and the emergence of secondary CuO and Cu₂O phases at higher Cu levels, suggesting solubility thresholds. SEM analysis revealed morphological evolution from spherical to rod-like structures, and EDX confirmed effective dopant incorporation. UV–Vis spectroscopy demonstrated bandgap tunability from 4.54 to 4.33 eV, influenced by doping-induced defect states and crystallite size variation. FTIR spectra revealed characteristic Mg–O and Cu–O stretching vibrations, as well as surface hydroxyl groups. Magnetic measurements indicated room-temperature ferromagnetism arising from oxygen and cation vacancies. Additionally, photocatalytic experiments showed that the Cu0.03Zn0.03MgO composition achieved outstanding degradation efficiencies (85.2% for methylene blue, 85.2% for methyl orange, and 76.2% for rhodamine B) under UV light. The degradation performance was further modulated by dye concentration, catalyst loading, and the presence of radical scavengers. These findings demonstrate that Cu/Zn co-doped MgO nanoparticles possess highly tunable physicochemical properties, making them strong candidates for integration in UV-driven electronic, magnetic, and photocatalytic device platforms.