Room-Temperature Ferromagnetism in Mn-Doped ZnO Nanoparticles Synthesized by the Sol-Gel Method

被引:14
|
作者
Kanwal, Sidra [1 ]
Khan, Muhammad Tahir [1 ]
Tirth, Vineet [2 ,3 ]
Algahtani, Ali [2 ,3 ]
Al-Mughanam, Tawfiq [4 ]
Zaman, Abid [1 ]
机构
[1] Riphah Int Univ, Dept Phys, Islamabad 44000, Pakistan
[2] King Khalid Univ, Coll Engn, Mech Engn Dept, Abha 61421, Asir, Saudi Arabia
[3] King Khalid Univ, Res Ctr Adv Mat Sci RCAMS, Abha 61413, Asir, Saudi Arabia
[4] King Faisal Univ, Coll Engn, Dept Mech Engn, Al Hasa 31982, Saudi Arabia
来源
ACS OMEGA | 2023年 / 8卷 / 31期
关键词
OPTICAL-PROPERTIES; MAGNETIC-PROPERTIES; THIN-FILMS; MICROSTRUCTURE; CO;
D O I
10.1021/acsomega.3c03418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the current work,pure ZnO and Mn-doped ZnO nanoparticles weresynthesized by the sol-gel autocombustion method. Structuralanalysis and phase determination were done by X-ray diffraction, anda hexagonal wurtzite structure was exhibited with disparate microstructuresfor all samples. Mn2+ ions were well composed, as evidencedby the fluctuation of lattice parameters, dislocation density, andlattice strain. Crystallite size decreases from 38.42 to 27.54 nmby increasing the doping concentration. Field emission scanning electronmicroscopy results shows the combination of evenly distributed spherical-likeand hexagon-like structures. Fourier transform infrared spectra revealedthat when Mn content increased, the absorption bands red-shifted.The drop in the energy band gap from 3.25 eV for ZnO to 2.99 eV forZn(0.96)Mn(0.04)O was predicted by ultraviolet-visibleabsorption spectra. This red shift in the energy band gap can be explainedby the sp-d exchange interaction between the band electronsof ZnO and localized d electrons of Mn. A study of magnetic propertiesrevealed the change of the diamagnetic attribute for pure ZnO to theroom-temperature ferromagnetic attribute of doped samples. In thecurrent study, room-temperature ferromagnetism was achieved for Mn-dopedZnO nanoparticles, which can serve as a desirable option for practicalapplications in the future.
引用
收藏
页码:28749 / 28757
页数:9
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