X-ray excited optical luminescence studies of ZnO and Eu-doped ZnO nanostructures

被引:87
|
作者
Armelao, L.
Heigl, F.
Jurgensen, A.
Blyth, R. I. R.
Regier, T.
Zhou, X.-T.
Sham, T. K.
机构
[1] Univ Padua, Dept Chem, ISTM, CNR, I-35131 Padua, Italy
[2] Univ Padua, INSTM, I-35131 Padua, Italy
[3] Univ Wisconsin, Canadian Synchrotron Radiat Facil, Ctr Synchrotron Radiat, Stoughton, WI 53589 USA
[4] Univ Saskatchewan, Canadian Light Source, Saskatoon, SK S7N 0X4, Canada
[5] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2007年 / 111卷 / 28期
关键词
D O I
10.1021/jp071379f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pure (ZnO) and Eu-doped ZnO (Eu:ZnO) nanostructures have been grown in different morphologies by thermal evaporation. The growth of the structures depends on the temperature and concentration gradient during material deposition as well as on the doping species. X-ray excited optical luminescence (XEOL) from nanostructured ZnO and Eu:ZnO shows a correlation of optical properties with morphology on a nanoscale. In particular, the relative intensity of band gap and defect emission (green light) changes drastically in Eu:ZnO and ZnO nanostructures with different morphology. In this Article, we present experimental results from Eu:ZnO and ZnO nanostructures, using synchrotron radiation-based XEOL, time-gated XEOL, and element specific XANES with partial and total photoluminescence yield (PLY). Our results suggest that the rare earth dopant most likely affects the energy transfer and structural changes by nucleation, rather than direct radiative decay from Eu sites.
引用
收藏
页码:10194 / 10200
页数:7
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