Infrared optical absorption in low-spin Fe2+-doped SrTiO3

被引:13
作者
Comes, Ryan B. [1 ]
Kaspar, Tiffany C. [1 ]
Heald, Steve M. [2 ]
Bowden, Mark E. [3 ]
Chambers, Scott A. [1 ]
机构
[1] Pacific NW Natl Lab, Phys & Computat Sci Directorate, 902 Battelle Blvd, Richland, WA 99352 USA
[2] Argonne Natl Lab, Adv Photon Source, 9700 S Cass Ave, Argonne, IL 60439 USA
[3] Pacific NW Natl Lab, Environm Mol Sci Lab, 902 Battelle Blvd, Richland, WA 99352 USA
关键词
SrTiO3; molecular beam epitaxy; x-ray absorption spectroscopy; x-ray photoelectron spectroscopy; ELECTRONIC-STRUCTURE; DOPED SRTIO3; GAP; FERROELECTRICITY; CONDUCTIVITY; SUBSTITUTION; CROSSOVER;
D O I
10.1088/0953-8984/28/3/035901
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Band gap engineering in SrTiO3 and related titanate perovskites has long been explored due to the intriguing properties of the materials for photocatalysis and photovoltaic applications. A popular approach in the materials chemistry community is to substitutionally dope aliovalent transition metal ions onto the B site in the lattice to alter the valence band. However, in such a scheme there is limited control over the dopant valence, and compensating defects often form. Here we demonstrate a novel technique to controllably synthesize Fe2+- and Fe3+-doped SrTiO3 thin films without formation of compensating defects by co-doping with La3+ ions on the A site. We stabilize Fe2+-doped films by doping with two La ions for every Fe dopant, and find that the Fe ions exhibit a low-spin electronic configuration, producing optical transitions in the near infrared regime and degenerate doping. The novel electronic states observed here offer a new avenue for band gap engineering in perovskites for photocatalytic and photovoltaic applications.
引用
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页数:7
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