Revealing the surface origin of green band emission from ZnO nanostructures by plasma immersion ion implantation induced quenching

2008 ◽  
Vol 103 (6) ◽  
pp. 064307 ◽  
Author(s):  
Y. Yang ◽  
X. W. Sun ◽  
B. K. Tay ◽  
Peter H. T. Cao ◽  
J. X. Wang ◽  
...  
2010 ◽  
Vol 114 (41) ◽  
pp. 17889-17893 ◽  
Author(s):  
Rui Chen ◽  
Yeeyan Tay ◽  
Jun Ye ◽  
Yang Zhao ◽  
Guozhong Xing ◽  
...  

2010 ◽  
Vol 108 (11) ◽  
pp. 113507 ◽  
Author(s):  
Yuanda Liu ◽  
Hongwei Liang ◽  
Lu Xu ◽  
Jianze Zhao ◽  
Jiming Bian ◽  
...  

2009 ◽  
Vol 105 (11) ◽  
pp. 113511 ◽  
Author(s):  
L. W. Chang ◽  
J. H. Cheng ◽  
C. H. Hsu ◽  
H. Y. Chao ◽  
W. Li ◽  
...  

2006 ◽  
Vol 957 ◽  
Author(s):  
Shiva S Hullavarad ◽  
P C Karulkar ◽  
R D Vispute ◽  
R Heng ◽  
T Venkatesan

ABSTRACTIn this paper we report the growth of ZnO nanowires (12-60 nm) and nanorods (500 nm) by a method of Catalysis Free Direct Vapor Phase (DVP) technique. The nanowires were grown on c-Al2O3 and pulsed laser deposited ZnO nucleation layer on Al2O3 substrates at 800 °C without employing any metal catalysts that are conventionally used in MOCVD or Vapor-Liquid-Solid phase techniques. The ZnO nanowires are found to emit UV light at 386 nm with considerably lower green band emission.


1968 ◽  
Vol 39 (5) ◽  
pp. 2413-2416 ◽  
Author(s):  
R. J. Carbone ◽  
M. M. Litvak

Vacuum ◽  
2013 ◽  
Vol 89 ◽  
pp. 163-167 ◽  
Author(s):  
R.M. Oliveira ◽  
M.S. Vieira ◽  
M. Ueda ◽  
A. Tóth

2006 ◽  
Vol 957 ◽  
Author(s):  
An-jen Cheng ◽  
Dake Wang ◽  
Hee Won Seo ◽  
Minseo Park ◽  
Yonhua Tzeng

ABSTRACTRoom temperature photoluminescence (PL) spectra from zinc oxide (ZnO) nanostructures were studied. ZnO samples were produced via thermal chemical vapor deposition (thermal-CVD) and a variety of ZnO nanostructures were synthesized by adjusting the oxygen content during the growth process. All samples exhibit a sharp and strong ultra-violet near-band-edge (NBE) emission at about 3.18 eV. The visible emission from the samples deposited under an oxygen-deficient condition were dominated by blue-green band emission at 2.34 eV. The intensity of the blue-green band was greatly reduced (so-called green band free) for the ZnO deposited at the center of the wafer while strong violet-blue emission bands and broad bands at yellow-orange-red range were collected from the ZnO grown along the edge of the wafer. We believe that the spatial inhomogeniety was caused by turbulent gas flow in the reaction chamber, which resulted in different local oxygen concentration. Origin of visible luminescence from ZnO nanostructures will be discussed and a model to explain the observed visible luminescence process will be presented.


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