Fast Mapping of the Cobalt-Valence State in Ba0.5Sr0.5Co0.8Fe0.2O3-d by Electron Energy Loss Spectroscopy

被引:25
|
作者
Mueller, Philipp [1 ,2 ]
Meffert, Matthias [1 ]
Stoermer, Heike [1 ]
Gerthsen, Dagmar [1 ,2 ]
机构
[1] KIT, Lab Elektronenmikroskopie, D-76131 Karlsruhe, Germany
[2] KIT, DFG, CFN, D-76131 Karlsruhe, Germany
关键词
BSCF; EELS; TEM; cobalt; Co-valence; white-line; transition metal; PCA; oxidation state; TRANSITION-METAL OXIDES; 2P ABSORPTION-SPECTRA; X-RAY-ABSORPTION; PEROVSKITE; SEPARATION; MEMBRANES; DECOMPOSITION; MICROSCOPY; STABILITY; PHASE;
D O I
10.1017/S1431927613013536
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A fast method for determination of the Co-valence state by electron energy loss spectroscopy in a transmission electron microscope is presented. We suggest the distance between the Co-L-3 and Co-L-2 white-lines as a reliable property for the determination of Co-valence states between 2+ and 3+. The determination of the Co-L-2,L-3 white-line distance can be automated and is therefore well suited for the evaluation of large data sets that are collected for line scans and mappings. Data with a low signal-to-noise due to short acquisition times can be processed by applying principal component analysis. The new technique was applied to study the Co-valence state of Ba0.5Sr0.5Co0.8Fe0.2O3-d (BSCF), which is hampered by the superposition of the Ba-M-4,M-5 white-lines on the Co-L-2,L-3 white-lines. The Co-valence state of the cubic BSCF phase was determined to be 2.2+ (+/- 0.2) after annealing for 100 h at 650 degrees C, compared to an increased valence state of 2.8+ (+/- 0.2) for the hexagonal phase. These results support models that correlate the instability of the cubic BSCF phase with an increased Co-valence state at temperatures below 840 degrees C.
引用
收藏
页码:1595 / 1605
页数:11
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