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Electron Paramagnetic Resonance Study on Oxygen Vacancies and Site Occupations in Mg-Doped BaTiO3 Ceramics

机译:Mg掺杂BATIO3陶瓷中氧空位和现场职业的电子顺磁共振研究

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摘要

Nominal (Ba1−xMgx)TiO3 (x = 0.015) (BM1T) and (Ba1−xMgx)TiO3 (x = 0.03−0.20) (BMT) ceramics were prepared by the mixed-oxide route at sintering temperatures (Ts) of 1200−1400 °C and 1200 °C, respectively. The solubility limit of Mg2+ in BMT was determined by XRD to be x = 0.05, and evidence was found for occupation of the A site by Mg2+. Electron paramagnetic resonance (EPR) was employed as a key technique to investigate the effect of Ts on oxygen vacancies in BM1T. The structure of BM1T changed from pseudocubic at Ts = 1200 °C to tetragonal at 1300 °C to mixed phases of hexagonal and tetragonal at 1400 °C. When Ts ≥ 1300 °C, a g = 1.956 EPR signal was observed at T = −188 °C and assigned as ionized oxygen vacancies. Mg2+ exhibited amphoteric behavior of substituting for the double cation sites. When Ts = 1400 °C, B-site Mg2+ and oxygen vacancies mainly existed in the hexagonal phase and A-site Mg2+ was dominant in the tetragonal phase. The higher tan δ was attributed to the higher concentrations of oxygen vacancies and Ti3+ in the hexagonal phase.
机译:在烧结温度(TS)为1200-的混合氧化物途径制备标称(X = 0.015)TiO3(X = 0.015)和(BA1-XMGX)TiO3(X = 0.03-0.20)(BMT)陶瓷分别为1400°C和1200°C。通过XRD测定Mg2 +在BMT中的溶解度极限为x = 0.05,并且发现证据通过Mg2 +占据A位点。采用电子顺磁共振(EPR)作为研究TS对BM1T氧空位的影响的关键技术。 BM1T的结构从TS = 1200℃的假序在1300℃下变为四边形,以在1400℃下在六边形和四边形的混合相。当TS≥1300℃时,在T = -188℃下观察到G = 1.956 EPR信号,并分配为电离氧空位。 Mg2 +表现出反应替代双阳离子位点的两性行为。当TS = 1400℃,B位Mg2 +和氧空位主要存在于六边形相位和A位Mg2 +中,在四方相中显着。较高的TANδ归因于六边形相中较高浓度的氧空位和TI3 +。

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