Hostname: page-component-848d4c4894-x24gv Total loading time: 0 Render date: 2024-06-10T23:34:00.098Z Has data issue: false hasContentIssue false

Synthesis of Well-aligned ZnO Nanowires Using Simple Physical Vapor Deposition without Catalysts or Additives

Published online by Cambridge University Press:  15 February 2011

Lisheng Wang
Affiliation:
The Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084, China
Xiaozhong Zhang
Affiliation:
The Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084, China
Songqing Zhao
Affiliation:
Institute of Physics and Center for Condensed Matter Physics, Chinese Academy of Sciences, Beijing 100080, China
Guoyuan Zhou
Affiliation:
Institute of Physics and Center for Condensed Matter Physics, Chinese Academy of Sciences, Beijing 100080, China
Yueliang Zhou
Affiliation:
Institute of Physics and Center for Condensed Matter Physics, Chinese Academy of Sciences, Beijing 100080, China
Junjie Qi
Affiliation:
Institute of Physics and Center for Condensed Matter Physics, Chinese Academy of Sciences, Beijing 100080, China
Get access

Abstract

Well-aligned ZnO nanowires were synthesized by simple physical vapor deposition using c-oriented ZnO thin films as substrate without catalysts or additives. The synthesized ZnO nanowires have two typical average diameters: 60 nm in majority and 120 nm in minority. They are about 4ím in length and well aligned along the normal direction of the substrate. Most of the synthesized ZnO nanowires are single crystalline in a hexagonal structure and grow along the [001] direction. The c-oriented ZnO thin films control the growth direction. Photoluminescence spectrum was measured showing a single strong ultraviolet emission (380 nm). Such result indicates that the ZnO nanowire arrays can be applied to excellent optoelectronic devices.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Wong, E.M. and Searson, P.C., Appl. Phys. Lett 74, 2939 (1999).Google Scholar
2 Huang, M.H., Mao, S., Feick, H., Yan, H., Wu, Y., Kind, H., Weber, E., Russo, R., and Yang, P., Science 292, 1897 (2001).Google Scholar
3 Vayssieres, L., Adv. Mater. 15, 464 (2003).Google Scholar
4 Liu, C., Zapien, J.A., Yao, Y., Meng, X., Lee, C.S., Fan, S., Lifshitz, Y., and Lee, S.T., Adv. Mater. 15, 838 (2003).Google Scholar
5 Greene, L.E., Law, M., Goldberger, J., Kim, F., Johnson, J.C., Zhang, Y., Saykally, R.J., and Yang, P., Angew. Chem. 42, 3031 (2003).Google Scholar
6 Li, S.Y., Lee, C.Y., Tseng, T.Y., J. Cryst. Growth 247, 357 (2003).Google Scholar
7 Gao, P.X., Ding, Y., and Wang, Z.L., Nano Letters 3, 1315 (2003).Google Scholar
8 Lyu, S.C., Zhang, Y., Lee, C.J., Ruh, H. and Lee, H.J., Chem. Mater. 15, 3294 (2003).Google Scholar
9 Tseng, Y.-K., Huang, C.-J., Cheng, H.-M., Liu, K.-S., and Chen, I-C., Adv. Funct. Mater. 13, 811 (2003).Google Scholar
10 Kima, T.-W., Kawazoe, T., Yamazaki, S., Ohtsu, M. and Sekiguchi, T., Appl. Phys. Lett. 84, 3358 (2004).Google Scholar
11 Yao, B. D., Chan, Y. F., and Wang, N., Appl. Phys. Lett. 81, 757 (2002).Google Scholar
12 Yu, W. D., Li, X. M., and Gao, X. D., Appl. Phys. Lett. 84, 2658 (2004).Google Scholar
13 Wagner, R.S., Ellis, W.C., Appl. Phys. Lett. 4, 89 (1964).Google Scholar
14 Yang, P., Lieber, C.M., J. Mater. Res. 12, 2981 (1997).Google Scholar
15 Zhang, Y., Wang, N., Gao, S., He, R., Miao, S., Liu, J., Zhu, J., and Zhang, X., Chem. Mater. 14, 3564 (2002).Google Scholar
16 Wang, Z.L., J. Phys.: Condens. Matter 16, R825 (2004).Google Scholar
17 Kong, Y. C., Yu, D. P., Zhang, B., Fang, W., and Feng, S. Q., Appl. Phys. Lett. 78, 407 (2001).Google Scholar
18 Egelhaaf, H.-J., Oelkrug, D., J. Cryst. Growth 161, 190 (1996).Google Scholar