Published April 15, 2010 | Version v1
Journal article

Magnetic, magnetoresistance and electrical transport properties of Ni and Al co-doped ZnO films grown on glass substrates by direct current magnetron co-sputtering

  • 1. Department of Physics, School of Applied Science, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China)
  • 2. Department of Mathematics and Physics, Beijing Technology and Business University, 33 Fucheng Road, Haidian District, Beijing 100037 (China)

Description

200-nm-thick Zn0.85Al0.04Ni0.11O films were deposited on glass substrates at 300 K and 573 K by co-sputtering ZnO:Al and Ni targets. A temperature dependence of magnetization and resistivity within 50-300 K and a room temperature magnetoresistance (MR) were measured. X-ray photoelectron spectroscopy was used to analyze chemical valences of Ni in the films. The films have the room temperature ferromagnetism. A magnetization of the film grown at 300 K decreases slightly and that of the film grown at 573 K decreases markedly with increasing temperature. The small negative MR is observed for the film deposited at 300 K while the positive MR is obtained for the film prepared at 573 K. For the film grown at 300 K, the carrier transport mechanism is thermally activated band conduction. However, the carrier transport mechanism in the film grown at 573 K is the Mott's variable range hopping in the temperature range below 100 K and the thermally activated band conduction above 140 K. The metallic Ni atoms and Ni2+ ions exist in the films. The ferromagnetism is mainly attributed to the Ni clusters in the Zn0.85Al0.04Ni0.11O film.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2009.12.007

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2009.12.007;
PII
S0254-0584(09)00753-6;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
120
Journal Issue
2-3
Journal Page Range
p. 571-575
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.