Published December 14, 2012 | Version v1
Journal article

Tuning photoluminescence properties of ZnO nanorods via surface modification

  • 1. University of Chinese Academy of Sciences, Beijing 100049 (China)
  • 2. National Center for Nanoscience and Technology, Beijing 100190 China (China)

Description

Zinc oxide (ZnO) is a versatile material that has been used in photocatalysis, solar cells, chemical sensors, and piezoelectric transducers. All these are directly related to its surface properties. Here ZnO nanorod arrays were successfully synthesized by electrochemical deposition method, the surface of which was modified by dopamine, a robust anchor. Compared with pristine ZnO sample, the surface modification can greatly enhance the ultraviolet and visible-light photoluminescence. This is due to the formation of polydopamine on the nanorod surface, which may act as a dye that can be photoexcited. The resultant photogenerated electrons can inject into the conduction band of ZnO and take part in the luminescent process. These results may provide a foundation for real applications of ZnO nanomaterials in optoelectronic devices and, especially, for the applications in biological field as both the dopamine and ZnO are biocompatible materials. -- Highlights: ► ZnO nanorod arrays are prepared via a simple electrochemical deposition method. ► Photoluminescence of ZnO nanorods can be greatly enhanced via dopamine treatment. ► Dye-like polydopamine can be formed on the nanorod surface upon dopamine treatment. ► Photogenerated electrons in polydopamine can inject into conduction band of ZnO. ► Enhanced photoluminescence is because more electrons can contribute to it.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2012.09.065

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2012.09.065;
PII
S0254-0584(12)00891-7;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
137
Journal Issue
2
Journal Page Range
p. 622-627
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.