期刊
MATERIALS
卷 15, 期 19, 页码 -出版社
MDPI
DOI: 10.3390/ma15196652
关键词
europium titanate; EuTiO3; ferroelectric; ferromagnetic; multiferroic
类别
资金
- Ministry of Science and Technology, Taiwan [MOST 110-2221-E-006-033, MOST 111-2221-E-006-154]
The study investigated the mixed valences and oxygen vacancies in Eu1-xBaxTi1-yMyO3 materials, as well as the impact of Co2+/Ni2+ co-doping on the material properties. Sintered at 1400 degrees Celsius, the Co2+/Ni2+ co-doping in Eu1-xBaxTi1-yMyO3 materials can result in a transition from antiferromagnetic to ferromagnetic, possibly due to the asymmetric distortion of the Eu-O polyhedron.
Eu1-xBaxTi1-yMyO3 (M = Co or Ni) was sintered at 1400 degrees C under a reduction atmosphere. X-ray photoelectron spectroscopy revealed the mixed valences of Eu2+/Eu3+ and Ti4+/Ti3+ in EuTiO3 and Eu0.7Ba0.3TiO3, as well as some oxygen vacancies required to keep the charge neutrality. The co-doping of Co2+/Ni2+ in Eu0.7Ba0.3TiO3 resulted in the disappearance of oxygen vacancies, as a result of a reduction in Ti3+ numbers and an increase in Eu3+ numbers. On the other hand, Ba2+ doping led to an increased lattice parameter due to its larger ionic size than Eu2+, whereas the Co2+/Ni2+ co-doping resulted in smaller lattice parameters because of the combined effects of ionic size and variation in the oxygen-vacancy numbers. Eu0.7Ba0.3TiO3 exhibited a clear ferroelectricity, which persisted in the Co2+/Ni2+ co-doped samples until the doping levels of y = 0.05 and 0.10, respectively. Eu0.7Ba0.3TiO3 remained to be antiferromagnetic with a reduced transition temperature of 3.1 K, but co-doping of Co2+/Ni2+ turned the samples from antiferromagnetic to ferromagnetic with transition temperatures of 2.98 K and 2.72 K, respectively. The cause for such a transition could not be explained by the larger lattice volume, oxygen vacancies and mixed valences of Eu2+/Eu3+, which were proposed in previous works. Instead, it was more likely to arise from a large asymmetric distortion of the Eu-O polyhedron introduced by the aliovalent doping, which promotes the admixture of Eu 5d and 4f states.
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