| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1523339 | Materials Chemistry and Physics | 2012 | 5 Pages |
The Cu-doped hydrogen titanate nanorods are synthesized via a hydrothermal reaction and converted into Cu-doped TiO2(B) and anatase phases by calcinations. X-ray diffraction (XRD), Fourier transform infrared (FTIR) and selected area electron diffraction (SAED) pattern do not show the presence of any other phases and thus confirmed the intrinsic ferromagnetic behavior rather than it arising from metallic clusters. The blue shifting in absorption edge and increase in photoluminescence (PL) intensity from Cu-doped hydrogen titanate to anatase phase are strongly correlated with concentration of oxygen vacancies and defect formation. The higher concentration of oxygen vacancies and/or structural defects leads to the coalescence of ferromagnetic domains, which corroborates to the observed higher magnetization value of Cu-doped anatase phase compared to other phases.
Graphical abstractRoom temperature ferromagnetic behavior has been observed in the Cu-doped titanate, TiO2(B) and anatase nanorods. Oxygen vacancies and/or structural defects are responsible for the observed ferromagnetism.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The Cu-doped titanate nanorods have been synthesized by hydrothermal method. ► Ferromagnetism of Cu-doped TiO2 nanorods are intrinsic property. ► Room temperature ferromagnetism observed in all the Cu-doped samples. ► Variation in Ms is attributed due to oxygen vacancies and defect formation.
