Relation between process parameters of ZnO host films and optical activation of doped Er3+ ions

被引:15
作者
Akazawa, Housei [1 ]
Shinojima, Hiroyuki [2 ]
机构
[1] NTT Microsyst Integrat Labs, Atsugi, Kanagawa 2430198, Japan
[2] Kurume Natl Coll Technol, Kurume, Fukuoka 8308555, Japan
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2014年 / 189卷
关键词
ZnO:Er; Photoluminescence; Concentration quenching; 1.54 mu m; Sputtering; M EMISSION DYNAMICS; SOL-GEL METHOD; THIN-FILMS; UP-CONVERSION; IMPLANTED ZNO; LUMINESCENCE; TEMPERATURE; DEPOSITION;
D O I
10.1016/j.mseb.2014.07.007
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We investigated how the crystallinity of ZnO host films deposited on Si(1 0 0) substrates by electron cyclotron resonance (ECR) plasma sputtering affects the optical activity of Er3+ ions doped in them under resonant excitation with 532-nm laser light. Photoluminescence from ZnO:Er films deposited at room temperature (RT) exhibited a main emission peak at 1538 nm with a sub-peak at 1553 nm. The emission intensity reached a steady state at Er content between 0.6 and 3 at.%, and attenuated above 3 at.%. This concentration quenching correlates with derivation of X-ray diffraction angles from the Vegard's law. Deposition at RT produced non-equilibrium state of ZnO:Er films possibly stabilized with vacancies to maintain charge neutrality. After post annealing of ZnO:Er films with Er content less than 1 at.%, the emission intensities were markedly reduced as the crystalline lattice was rearranged. For films in the concentration quenching range, however, post annealing increased the emission peak width while maintaining emission intensity, indicating that Er3+ ions migrated and populated various emission-active sites. In this case, the main peak wavelength blue shifted to 1536 nm and produced a new sub peak at 1546 nm. When the deposition temperature exceeded 500 degrees C, emissions from Er3+ ions were greatly enhanced. This will result from improvement in crystallinity and fixing Er3+ ions at six-fold coordinated C-4v symmetry sites. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 44
页数:7
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