Layer-by-Layer Epitaxial Growth of Defect-Engineered Strontium Cobaltites

被引:22
作者
Andersen, Tassie K. [1 ,2 ]
Cook, Seyoung [1 ,2 ]
Wan, Gang [1 ]
Hong, Hawoong [3 ]
Marks, Laurence D. [2 ]
Fong, Dillon D. [1 ]
机构
[1] Argonne Natl Lab, Div Mat Sci, 9700 S Cass Ave, Argonne, IL 60439 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
关键词
metal oxides; strontium cobalt oxide; molecular beam epitaxy; defects in oxides; perovskite oxides; thin films; RUDDLESDEN-POPPER PHASES; X-RAY-SCATTERING; IN-SITU; SRCOO2.5; FILMS; DECOMPOSITION; PEROVSKITES; TEMPERATURE; STABILITY; KINETICS;
D O I
10.1021/acsami.7b16970
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Control over structure and composition of (ABO(3)) perovskite oxides offers exciting opportunities since these materials possess unique, tunable properties. Perovskite oxides with cobalt B-site cations are particularly promising, as the range of the cations stable oxidation states leads to many possible structural frameworks. Here, we report growth of strontium cobalt oxide thin films by molecular beam epitaxy, and conditions necessary to stabilize different defect concentration phases. In situ X-ray scattering is used to monitor structural evolution during growth, while in situ X-ray absorption near-edge spectroscopy is used to probe oxidation state and measure changes to oxygen vacancy concentration as a function of film thickness. Experimental results are compared to kinetically limited thermodynamic predictions, in particular, solute trapping, with semiquantitative agreement. Agreement between observations of dependence of cobaltite phase on oxidation activity and deposition rate, and predictions indicates that a combined experimental/theoretical approach is key to understanding phase behavior in the strontium cobalt oxide system.
引用
收藏
页码:5949 / 5958
页数:10
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