TY - GEN
T1 - Visible luminescence from ZnO nanostructures
AU - Cheng, An Jen
AU - Wang, Dake
AU - Seo, Hee Won
AU - Park, Minseo
AU - Tzeng, Yonhua
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2007
Y1 - 2007
N2 - Room 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 bluegreen 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.
AB - Room 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 bluegreen 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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M3 - Conference contribution
AN - SCOPUS:34250858328
SN - 0762313951
SN - 9780762313952
T3 - Materials Research Society Symposium Proceedings
SP - 277
EP - 282
BT - Zinc Oxide and Related Materials
T2 - 2006 MRS Fall Meeting
Y2 - 27 November 2006 through 1 December 2006
ER -