Heterojunction band offsets and dipole formation at BaTiO3/SrTiO3 interfaces

被引:34
作者
Balaz, Snjezana [1 ]
Zeng, Zhaoquan [2 ]
Brillson, Leonard J. [2 ,3 ]
机构
[1] Youngstown State Univ, Dept Phys & Astron, Youngstown, OH 44555 USA
[2] Ohio State Univ, Dept Elect & Comp Engn, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Phys, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
RESOLVED CATHODOLUMINESCENCE; THIN-FILMS; SRTIO3; VALENCE; BATIO3; SPECTROSCOPY; TITANATE; DEFECTS;
D O I
10.1063/1.4829695
中图分类号
O59 [应用物理学];
学科分类号
摘要
We used a complement of photoemission and cathodoluminescence techniques to measure formation of the BaTiO3 (BTO) on SrTiO3 (STO) heterojunction band offset grown monolayer by monolayer by molecular beam epitaxy. X-ray photoemission spectroscopy (XPS) provided core level and valence band edge energies to monitor the valence band offset in-situ as the first few crystalline BTO monolayers formed on the STO substrate. Ultraviolet photoemission spectroscopy (UPS) measured Fermi level positions within the band gap, work functions, and ionization potentials of the growing BTO film. Depth-resolved cathodoluminescence spectroscopy measured energies and densities of interface states at the buried heterojunction. Kraut-based XPS heterojunction band offsets provided evidence for STO/BTO heterojunction linearity, i.e., commutativity and transitivity. In contrast, UPS and XPS revealed a large dipole associated either with local charge transfer or strain-induced polarization within the BTO epilayer. (c) 2013 AIP Publishing LLC.
引用
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页数:9
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