EPR study on magnetic Zn1-xMnxO

in: Superlattices and Microstructures (2005)
Diaconu, Mariana; Schmidt, Heidemarie; Pöppl, Andreas; Böttcher, Rolf; Hoentsch, Joachim; Rahm, Andreas; Hochmuth, Holger; Lorenz, Michael; Grundmann, Marius
Diluted magnetic semiconductors (DMS), systems formed by replacing cations of the host semiconductor material with transition-metal ions, are developed for further use in spintronics. A good combination as a DMS is Zn1−xMnxO due to the ZnO wide band gap (3.37 eV) and the matching ionic radii of Mn2+ and Zn2+. Using electron paramagnetic resonance we determined the valence of Mn ions in Zn1−xMnxO thin films to be 2+. This is required for explaining the origin of the room temperature ferromagnetism observed in Zn1−xMnxO films.We studied films grown on c-plane sapphire substrates by pulsed laser deposition with the Mn content ranging from x = 0.001 to x = 0.091 and a single crystal with x = 0.035 for comparison. We observed the hyperfine and fine-structure lines of Mn2+ for x = 0.001, while for higher Mn contents the fine-structure lines were broadened by dipolar interactions and onto these lines a very broad single line, due to Mn ions in higher local concentrations, was superposed. We modeled the experimental spectra and separated the broad single line from the hyperfine and fine-structure lines. The hyperfine and fine-structure parameters obtained have values characteristic for Zn1−xMnxO lattice sites. We found that the D fine-structure parameter depends on the lattice distortion and Mn content. For example |D| amounts to 675 MHz for a single crystal with x = 0.035 and to 757 MHz for a film on c-plane sapphire with x = 0.001.

Third party cookies & scripts

This site uses cookies. For optimal performance, smooth social media and promotional use, it is recommended that you agree to third party cookies and scripts. This may involve sharing information about your use of the third-party social media, advertising and analytics website.
For more information, see privacy policy and imprint.
Which cookies & scripts and the associated processing of your personal data do you agree with?

You can change your preferences anytime by visiting privacy policy.