(La3+ Mg2+) codoped BiFeO3 nanopowders: Synthesis, characterizations, and giant dielectric relaxations

Main Article Content

Pornsawan Kum-onsa
Narong Chanlek
Masaki Takesada
Pornjuk Srepusharawoot
Prasit Thongbai

Abstract

A new strategy to improve the dielectric properties of BiFeO3 is proposed by codoping with La3+ and Mg2+ to control the ceramic microstructure and increase the dielectric permittivity (e¢), respectively. The main phase of BiFeO3 is obtained in nanocrystalline powders of LaxBi1-xFe1-xMgxO3 (x = 0, 0.05 and 0.1), which are prepared by a chemical co-precipitation method. The particle size of the codoped LaxBi1-xFe1-xMgxO3 is smaller than that of the BiFeO3. A dense ceramic microstructure without porosity is obtained by sintering at 800 °C for 3 h. The mean grain size of the BiFeO3 ceramics decreases with increasing codoping (La3+-Mg2+) concentration. The primary roles of La3+ and Mg2+ are to suppress the grain growth and enhance the densification rate, respectively. At 1 kHz, the e¢ of the LaxBi1-xFe1-xMgxO3 with x = 0.1 increased significantly compared to that of the BiFeO3, while the loss tangent (tand) was lower than that of the BiFeO3. In addition, another role of Mg2+ is to increase the e¢ without any effect on the tand. Two dielectric relaxations are observed in low-frequency (150-250 K) and high-temperature (250-400 K) ranges. An X-ray photoelectron spectroscopy shows that the Fe2+/Fe3+ ration in the codoped LaxBi1-xFe1-xMgxO3 increased compared to that of the BiFeO3, corresponding to the increase in e¢. Thus, a low-temperature dielectric relaxation is attributed to the electron hopping between Fe2+-O-Fe3+. On the other hand, a high-temperature dielectric relaxation is caused by interfacial polarization relaxation.

Article Details

How to Cite
Kum-onsa, P. ., Chanlek, N. ., Takesada, M. ., Srepusharawoot, P. ., & Thongbai, P. . (2021). (La3+ Mg2+) codoped BiFeO3 nanopowders: Synthesis, characterizations, and giant dielectric relaxations. Engineering and Applied Science Research, 48(6), 766–772. Retrieved from https://ph01.tci-thaijo.org/index.php/easr/article/view/244868
Section
ORIGINAL RESEARCH

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