An interesting new dilute magnetic compositions have been synthesized by solid-state reaction from (Gd, Ru), (Gd, Mn) and (Gd, Fe) codoped SrTiO3 semiconductors. The X-ray diffraction (XRD) patterns of pure, (Gd, Ru), (Gd, Mn) and (Gd, Fe) codoped SrTiO3 samples verified the formation of cubic SrTiO3 structure. The morphological analysis using scanning electron microscope (SEM) showed that the addition of (Gd, Ru), (Gd, Mn) and (Gd, Fe) ions obviously effect on the grains size and shape of SrTiO3 powder. The band gap energy of SrTiO3 powder was found to be 3.22 eV, and when (Gd, Ru), (Gd, Mn) and (Gd, Fe) ions incorporated into its lattice a blue shift to 3.28, 3.29 and 3.295 eV were detected, respectively. The X-Ray photoelectron spectroscopy (XPS) analysis of (Gd, Mn) codoped SrTiO3 composition (best ferromagnetic sample) ruled out the presence of Gd and Mn metals and confirmed the existence of Gd3+ and Mn2+ oxidation states. The measured magnetic results indicated that (Gd, Ru), (Gd, Mn) and (Gd, Fe) dopants strongly advance the ferromagnetic nature of SrTiO3 structure. The H-M loop of (Gd, Mn) codoped SrTiO3 composition gives the best ferromagnetic order with detected saturation magnetization (MS), coercivity (HC) and retentivity (Mr) of 0.52 emu/g, 177 Oe and 0.054 emu/g, respectively. These outcomes established the promising room temperature ferromagnetic order of the fabricated compositions, especially Sr0.98Gd0.02Ti0.98Ru0.02O3 semiconductor for spin-electronics applications.
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