Enhanced photoluminescence characteristics and intrinsic ferromagnetism in Co-substituted CeO2 nanoparticles

被引:13
作者
Poornaprakash, B. [1 ]
Subramanyam, K. [2 ]
Kumar, Mirgender [3 ]
Kim, Y. L. [1 ]
Reddy, M. Siva Pratap [4 ]
机构
[1] Gangneung Wonju Natl Univ, Dept Elect Engn, Kangnung 25457, South Korea
[2] Siddharth Inst Engn Technol, Dept Phys, Puttur 517583, India
[3] Yeungnam Univ, Dept Elect Engn, Gyongsan 38541, South Korea
[4] Kyungpook Natl Univ, Sch Elect Engn, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
CeO2; Structural parameters; Photoluminescence; Intrinsic ferromagnetism; ROOM-TEMPERATURE FERROMAGNETISM; DOPED CEO2; PARTICLES; MECHANISM; EMISSION; FE;
D O I
10.1016/j.mssp.2020.105566
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The creation of oxide based magnetic materials has attracted a great deal of scientific attention, owing to their novel applications in optoelectronic, memory, and spintronic device applications. In this study, the authors report upon the structural, optical, and magnetic properties of Co-substituted CeO2 nanocrystals synthesized via the wet chemical precipitation method. The obtained nanoparticles show good crystallinity as well as an FCC structure with an Fm3m space group of host CeO2 lattice, as confirmed by an X-ray diffraction results. It is noted that Co substitution at low concentrations enhances the photoluminescence characteristics of CeO2 nano particles, while higher concentrations significantly reduce the intensity of PL emission, as revealed by PL studies. The estimated M H loops illustrate that pristine CeO2 shows a paramagnetic nature, while all Co-substituted samples were ferromagnetic in nature. Furthermore, magnetic parameters such as saturation magnetization (M-S) and residual magnetization (M-R) increased with the inclusion of Co content, reaching a maximum at 4 at% Co and quenching at 6 at% and 8 at% of Co-substitution. In particular, Ce1-xCoxO2 (x = 0.04) nanoparticles show better luminescence and magnetic characteristics than the remaining concentrations.
引用
收藏
页数:10
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