Blueshift of near band edge emission in Mg doped ZnO thin films and aging

被引:300
作者
Shan, FK
Kim, BI
Liu, GX
Liu, ZF
Sohn, JY
Lee, WJ
Shin, BC
Yu, YS [1 ]
机构
[1] Dong Eui Univ, Elect Ceram Ctr, Pusan 614714, South Korea
[2] Acad Sinica, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
关键词
D O I
10.1063/1.1690091
中图分类号
O59 [应用物理学];
学科分类号
摘要
Pure and Mg doped ZnO thin films were deposited at 400 degreesC on glass substrates by pulsed laser deposition. An x-ray diffractometer (XRD) was used to investigate the structural properties of the thin films. It is found that all the thin films have a preferred (002) orientation. The peak position of (002) orientation is found to shift from 34.39degrees to 34.55degrees. The lattice constants of ZnO thin films were also obtained from XRD data. It is found that, with the increase of the dopant concentration, the lattice constant a decreases from 3.25 to 3.23 Angstrom, and c decreases from 5.20 to 5.16 Angstrom. From the spectrophotometer transmittance data, the band gap energies of the thin films were calculated by a linear fitting process. The band gap energy of Mg doped ZnO thin film increases with increasing dopant concentration. In photoluminescence (PL) spectra, two PL emission peaks are found in pure ZnO thin films, one is the near band edge (NBE) emission at 3.28 eV, and the other is green-yellow-red emission at around 2.4 eV. However, with the increase of the dopants, no green-yellow-red emissions are found in PL of Mg doped ZnO thin films. The NBE emission has a blueshift compared with that of pure ZnO thin film (as much as 0.12 eV). As time goes on, NBE emission in pure ZnO thin film is enhanced, and the green-yellow-red emissions disappear. (C) 2004 American Institute of Physics.
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页码:4772 / 4776
页数:5
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