Magnetic properties of Fe-doped NiO nanoparticles

被引:0
作者
de Brito, Alex Soares [1 ]
Valerio-Cuadros, Marlon Ivan [1 ,2 ]
Tupan, Lilian Felipe Silva [1 ,3 ]
Oliveira, Aline Alves [1 ]
Barco, Reginaldo [1 ]
Ivashita, Flavio Francisco [1 ]
Passamani, Edson Caetano [4 ]
de Araujo, Jose Humberto [5 ]
Torres, Marco Antonio Morales [5 ]
Paesano, Andrea [1 ,5 ]
机构
[1] Univ Estadual Maringa, Dept Fis, Ave Colombo,5790,Jardim Univ, Maringa, PR, Brazil
[2] Univ Nacl Mayor San Marcos, Fac Ciencias Fis, Lima, Peru
[3] Ctr Univ Inga, BR-87035510 Maringa, PR, Brazil
[4] Univ Fed Espirito Santo, Dept Fis, BR-29075910 Vitoria, ES, Brazil
[5] Univ Fed Rio Grande Norte UFRN, Dept Informat & Matemat Aplicada, Natal, RN, Brazil
关键词
Nanoparticles; Nickel oxide; Fe-doped; Core-shell model; Spin-glass; Cluster-glass; BEHAVIOR; TEMPERATURE; RELAXATION;
D O I
10.1016/j.heliyon.2023.e22876
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Undoped and Fe-doped NiO nanoparticles were successfully synthesized using a lyophilization method and systematically characterized through magnetization techniques over a wide temperature range, with varying intensity and frequency of the applied magnetic fields. The Ni1xFexO nanoparticles can be described by a core-shell model, which reveals that Fe doping enhances exchange interactions in correlation with nanoparticle size reduction. The nanoparticles exhibit a superparamagnetic blocking transition, primarily attributed to their cores, at temperatures ranging from above room temperature to low temperatures, depending on the Fe-doping level and sample synthesis temperature. The nanoparticle shells also exhibit a transition at low temperatures, in this case to a cluster-glass-like state, caused by the dipolar magnetic interactions between the net magnetic moments of the clusters. Their freezing temperature shifts to higher temperatures as the Fe-doping level increases. The existence of an exchange bias interaction was observed, thus validating the core-shell model proposed.
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页数:11
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