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吉林化工学院学报, 2018, 35(1): 44-46     https://doi.org/10.16039/j.cnki.cn22-1249.2018.01.011
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Tm3+离子在BaTiO3介电陶瓷中的位占据研究
梁 月,路大勇
吉林化工学院 材料科学与工程研究中心,吉林大学 化学学院
Study on the Site Occupations of Tm3+ Ions in BaTiO3 Dielectric Ceramics
LIANG Yue,LU Da-yong
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摘要 TmBaTiO3晶格中的位占据一直是存在争议的问题.针对按照名义分子式制备的(Ba1-xTmx)Ti1-x/4O3(BTmT)和Ba(Ti1-xTmx) O3( BTTm) 陶瓷,采用 X 射线衍射(XRD)和电子顺磁共振(EPR)技术,鉴定 Tm3+离子在 BaTiO3 晶格中的位占据情况结果表明:Tm3+ BaTiO3晶格中的位占据与Ba/Ti比有关Ba /Ti>1 时,Tm3+离子基本不溶于 BaTiO3 晶格Ba /Ti<1 时, Tm3+ 离子在 BTmT 陶瓷中的固溶度为 x=0.02,且表现为四方钙钛矿结构; 通过晶胞体积比较可知, Tm3+ 显示同时占据 Ba 位和 Ti 位的双性行为,并表现出 Ba 位喜好倾向
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梁 月
路大勇
关键词:  钛酸钡  位占据  X 射线衍射  电子顺磁共振  点缺陷
    
Abstract: The site occupations of Tm3+ ions in the BaTiO3 lattice has always been a controversial problem.For
ceramics prepared according to the nominal formula
( Ba1-x Tmx ) Ti1-x/4 O3 ( BTmT) and Ba ( Ti1-x Tmx ) O3
( BTTm) , X-ray diffraction ( XRD) and electron paramagnetic resonance ( EPR) techniques were used to
identify the site occupations of Tm
3+ ions in the BaTiO3 lattice.The results indicated that the position of Tm3+ in
BaTiO
3 lattice is related to Ba /Ti ratio.In the case of Ba /Ti>1Tm3+ ions are basically insoluble in BaTiO3
lattice.When Ba /Ti<1the solubility limit of Tm3+ ions at the Ba-sites in BTmT ceramics is x = 0.02and these
ceramics exhibited a tetragonal perovskite structure. a conclusion can be drawn by comparing the volume of
crystal packages that Tm
3+ ions showed the amphoteric behavior that occupied Ba sites and Ti sites.
Key words:  BaTiO3    Site occupation    X-ray diffraction    electron paramagnetic resonance    point defect
               出版日期:  2018-01-25      发布日期:  2018-01-25      整期出版日期:  2018-01-25
O 614.23  
引用本文:    
梁 月, 路大勇. Tm3+离子在BaTiO3介电陶瓷中的位占据研究[J]. 吉林化工学院学报, 2018, 35(1): 44-46.
LIANG Yue, LU Da-yong. Study on the Site Occupations of Tm3+ Ions in BaTiO3 Dielectric Ceramics. Journal of Jilin Institute of Chemical Technology, 2018, 35(1): 44-46.
链接本文:  
https://xuebao.jlict.edu.cn/CN/10.16039/j.cnki.cn22-1249.2018.01.011  或          https://xuebao.jlict.edu.cn/CN/Y2018/V35/I1/44
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