Formation of structural defects and strain in electrodegraded Fe-doped SrTiO3 crystals due to oxygen vacancy migration

被引:20
作者
Ascienzo, David [1 ,2 ]
Kurt, Onur [1 ,3 ]
Greenbaum, Steve [1 ,2 ]
Bayer, Thorsten J. M. [4 ,5 ]
Maier, Russell A. [4 ,5 ]
Randall, Clive A. [4 ,5 ]
Ren, Yuhang [1 ,2 ]
机构
[1] CUNY, Hunter Coll, Phys & Astron, New York, NY 10021 USA
[2] CUNY, Grad Ctr, New York, NY USA
[3] CUNY City Coll, Elect Engn, New York, NY USA
[4] Penn State Univ, Mat Sci & Engn, University Pk, PA 16802 USA
[5] Penn State Univ, Inst Mat Res, University Pk, PA 16802 USA
关键词
electroceramic; oxygen vacancy; perovskite; raman spectroscopy; second harmonic generation; OPTICAL 2ND-HARMONIC GENERATION; DC ELECTRICAL DEGRADATION; PEROVSKITE-TYPE TITANATES; RESISTANCE DEGRADATION; INSULATION RESISTANCE; DIELECTRIC EVOLUTION; LOW-TEMPERATURE; THIN-FILMS; MODEL; SURFACE;
D O I
10.1111/jace.15407
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
We report on our investigation of structural defect and strain formation in electrodegraded reduced and oxidized, Fe-doped SrTiO3 (Fe:STO) single crystals using optical second harmonic generation (SHG) and confocal Raman spectroscopy. SHG and Raman spectra reveal structural and electrochemical inhomogeneity resulting from the formation of Fe4+/oxygen ion and Fe3+/oxygen vacancy aggregation sites along the degraded anode and cathode interfaces, respectively. We show that mixed Fe3+/Fe4+ states and structural strain gradients are generated across the color fronts. These results, as well as oxygen sublattice differences between the anodic and cathodic bulk, present the color front as an interface between two dominant oxygen bonding distortions. The strain near the color front shows a strong dependence on oxygen vacancy concentration and diffusion within the crystals. Our characterization of structural and electrochemical changes due to electric field-induced strain and oxygen vacancy migration advances knowledge of electrodegradation in perovskite-based titanate single crystals.
引用
收藏
页码:2545 / 2561
页数:17
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