Strong green emission in ZnO films after H2 surface treatment
Using a two-step fabrication technique (pulsed laser deposition (PLD) and H2 surface treatment), we fabricated ZnO thin films that could emit ultra-strong green emission with coexistence of random lasing phenomenon. After PLD deposition, the as-prepared undoped ZnO thin films (200–500 nm) were annea...
Saved in:
Main Authors: | , , , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2013
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/95985 http://hdl.handle.net/10220/11405 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-95985 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-959852020-03-07T14:02:45Z Strong green emission in ZnO films after H2 surface treatment Li, T. Herng, T. S. Liang, H. K. Bao, N. N. Wong, J. I. Xue, J. M. Chen, Tupei Ding, Jun School of Electrical and Electronic Engineering DRNTU::Engineering::Electrical and electronic engineering Using a two-step fabrication technique (pulsed laser deposition (PLD) and H2 surface treatment), we fabricated ZnO thin films that could emit ultra-strong green emission with coexistence of random lasing phenomenon. After PLD deposition, the as-prepared undoped ZnO thin films (200–500 nm) were annealed in Ar 95%–H25% ambient at 500 °C. The H2 treatment led to the formation of a porous structure that creates substantial optical cavities (diameter ~1.3 µm). Surprisingly, these optical cavities tremendously amplified the green emission rather than ultraviolet (UV) emission. There was insignificant change in emission intensity after high-temperature annealing (700 °C) in O2 and acetone dipping, indicating the samples are thermally and chemically stable. The samples exhibited a high quantum yield of 32%. We studied the origin of this ultra-strong green emission using low-temperature photoluminescence, extensive structural study and cyclic annealing. The results suggested that neither hydrogen nor VO plays a role in green emission. The green emission was attributed mainly to the complex defects and the presence of structural defects in the porous structure. In addition, we demonstrated the feasibility of large-scale green emission ZnO fabrication via micro-size patterning, paving a way to practical optoelectronic applications. 2013-07-15T04:39:24Z 2019-12-06T19:24:02Z 2013-07-15T04:39:24Z 2019-12-06T19:24:02Z 2012 2012 Journal Article Li, T., Herng, T. S., Liang, H. K., Bao, N. N., Chen, T., Wong, J. I., et al. (2012). Strong green emission in ZnO films after H 2 surface treatment. Journal of physics D : applied physics, 45(18). https://hdl.handle.net/10356/95985 http://hdl.handle.net/10220/11405 10.1088/0022-3727/45/18/185102 en Journal of physics D : applied physics © 2012 IOP Publishing Ltd. |
institution |
Nanyang Technological University |
building |
NTU Library |
country |
Singapore |
collection |
DR-NTU |
language |
English |
topic |
DRNTU::Engineering::Electrical and electronic engineering |
spellingShingle |
DRNTU::Engineering::Electrical and electronic engineering Li, T. Herng, T. S. Liang, H. K. Bao, N. N. Wong, J. I. Xue, J. M. Chen, Tupei Ding, Jun Strong green emission in ZnO films after H2 surface treatment |
description |
Using a two-step fabrication technique (pulsed laser deposition (PLD) and H2 surface treatment), we fabricated ZnO thin films that could emit ultra-strong green emission with coexistence of random lasing phenomenon. After PLD deposition, the as-prepared undoped ZnO thin films (200–500 nm) were annealed in Ar 95%–H25% ambient at 500 °C. The H2 treatment led to the formation of a porous structure that creates substantial optical cavities (diameter ~1.3 µm). Surprisingly, these optical cavities tremendously amplified the green emission rather than ultraviolet (UV) emission. There was insignificant change in emission intensity after high-temperature annealing (700 °C) in O2 and acetone dipping, indicating the samples are thermally and chemically stable. The samples exhibited a high quantum yield of 32%. We studied the origin of this ultra-strong green emission using low-temperature photoluminescence, extensive structural study and cyclic annealing. The results suggested that neither hydrogen nor VO plays a role in green emission. The green emission was attributed mainly to the complex defects and the presence of structural defects in the porous structure. In addition, we demonstrated the feasibility of large-scale green emission ZnO fabrication via micro-size patterning, paving a way to practical optoelectronic applications. |
author2 |
School of Electrical and Electronic Engineering |
author_facet |
School of Electrical and Electronic Engineering Li, T. Herng, T. S. Liang, H. K. Bao, N. N. Wong, J. I. Xue, J. M. Chen, Tupei Ding, Jun |
format |
Article |
author |
Li, T. Herng, T. S. Liang, H. K. Bao, N. N. Wong, J. I. Xue, J. M. Chen, Tupei Ding, Jun |
author_sort |
Li, T. |
title |
Strong green emission in ZnO films after H2 surface treatment |
title_short |
Strong green emission in ZnO films after H2 surface treatment |
title_full |
Strong green emission in ZnO films after H2 surface treatment |
title_fullStr |
Strong green emission in ZnO films after H2 surface treatment |
title_full_unstemmed |
Strong green emission in ZnO films after H2 surface treatment |
title_sort |
strong green emission in zno films after h2 surface treatment |
publishDate |
2013 |
url |
https://hdl.handle.net/10356/95985 http://hdl.handle.net/10220/11405 |
_version_ |
1681042015863701504 |