Impact of the change in charge compensation mechanism on the electrical, dielectric, and structural properties of La-doped BaTiO3 ceramics

被引:1
|
作者
Hwang, Seong-Mee [1 ]
Lim, Jong -Chan [2 ]
Kim, Sang-il [1 ]
Kim, Jeong-Yeon [1 ]
Hwang, Jihyun [2 ]
Lee, Chung-hyun [2 ]
Kwon, Namhee [3 ]
Kim, Inseo [4 ]
Lee, Kimoon [4 ]
Park, Soohyung [3 ,5 ]
Bae, Seung-Muk [6 ]
Hwang, Jin-Ha [2 ]
Lee, Kiyoung [2 ]
Kim, Hyun-Sik [1 ]
机构
[1] Univ Seoul, Dept Mat Sci & Engn, Seoul 02504, South Korea
[2] Hongik Univ, Dept Mat Sci & Engn, Seoul 04066, South Korea
[3] Korea Inst Sci & Technol KIST, Adv Anal Ctr, Seoul 02792, South Korea
[4] Kunsan Natl Univ, Dept Phys, Gunsan 54150, South Korea
[5] Univ Sci & Technol UST, KIST Sch, Div Nano & Informat Technol, Seoul 02792, South Korea
[6] Kunsan Natl Univ, Res Facil Ctr, Gunsan 54150, South Korea
基金
新加坡国家研究基金会;
关键词
La -doped BaTiO 3; Multilayer ceramic capacitor; Resistivity; Dielectric constant; Charge compensation; BARIUM-TITANATE; HYDROTHERMAL SYNTHESIS; CRYSTAL-STRUCTURE; POWDERS; SIZE; TEMPERATURE; BEHAVIOR; PARTICLE; DY;
D O I
10.1016/j.jeurceramsoc.2023.12.029
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
La-doped BaTiO3 ceramics are essential materials in electronic devices, finding applications in multilayer ceramic capacitors and positive temperature coefficient thermistors. While the electrical properties of La-doped BaTiO3 have been investigated, the impact of its room-temperature resistivity anomaly on dielectric properties remains unclear. We synthesized pristine and La-doped BaTiO3 (0.1 - 0.5 mol%) powders via hydrothermal methods, and then sintered bulk samples. Their resistivities (DC and AC), Curie temperature, room-temperature dielectric constant, and lattice volume with varying La doping concentrations were characterized. Beyond 0.3 mol%, the shift from electronic to ionic charge compensation mechanisms resulted in abrupt changes in resistivities, Curie temperature, and dielectric constant near 0.3 mol%. Given minimal changes in average grain size and relative density near 0.3 mol% La, the dominant factor influencing the dielectric constant peaking near this concentration was the shift in charge compensation mechanism.
引用
收藏
页码:5471 / 5479
页数:9
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