Synthesis and photoluminescence properties of hydrothemially-grown ZnO nanowires on the aerosol-deposited AZO seed layer

被引:8
|
作者
Lee, Jungkeun [1 ]
Lee, Soohwan [1 ]
Choi, Min-Geun [1 ]
No, Im-Jun [2 ]
Ryu, Jungho [3 ]
Dabra, Navneet [4 ,5 ,6 ]
Hundal, Jasbir S. [6 ]
Jeong, Dae-Yong [1 ]
机构
[1] Inha Univ, Sch Mat Sci & Engn, Inchon 402751, South Korea
[2] Inha Univ, Sch Elect Engn, Inchon 402751, South Korea
[3] Korea Inst Mat Sci, Funct Ceram Grp, Chang Won, South Korea
[4] Mata Sahib Kaur Girls Coll, Talwandi Sabo, Punjab, India
[5] Punjabi Univ, Patiala 147002, Punjab, India
[6] Giani Zail Singh Punjab Tech Univ, Dept Appl Phys, Mat Sci Lab, Bathinda 151001, Punjab, India
基金
新加坡国家研究基金会;
关键词
Nanocomposites; Optical properties; ZnO; Aerosol deposition; OPTICAL-PROPERTIES; EMISSION;
D O I
10.1016/j.ceramint.2014.03.054
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A nano-grained Al-doped ZnO (AZO) seed layer with three different Al contents was deposited on soda-lime glass substrates using an aerosol deposition (AD) method at room temperature. The AZO seed layer was polycrystalline with a dense structure and random orientation. The zinc oxide (ZnO) nanowires were hydrothermally synthesized at temperatures below 100 degrees C on the AZO AD seed layer. The hydrothermally-grown ZnO nanowires had a diameter less than 200 am and a wurtzite hexagonal structure with a preferred orientation along the c direction. The photoluminescence (PL) properties of the AZO AD seed layer films revealed only one peak in the ultra-violet (UV) range. The intensity at the near band edge (NBE) emission increased with decreasing Al content in the AZO AD seed layer. On the other hand, the hydrothermally-grown ZnO showed two peaks in the PL emission spectra located in the UV and visible range. The crystallinity and PL emission properties of the ZnO nanowires were enhanced by the hydrothermal process and the doping concentration in the seed layer without the need for an annealing process. (C) 2014 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:10693 / 10698
页数:6
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