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<title>Abstract</title> Barium titanate (Gd<sub>x</sub>Ba<sub>(1-x)</sub>TiO<sub>3</sub>) modified with replacing Barium (Ba) with Gadolinium (Gd) (x = 0, 0.25, 0.50, 0.625, 0.75, 0.875, and 1 Mol.%) were synthesized via the solid-state reaction method. This study elucidates the substitution mechanism of Gd<sup>3+</sup> ions into Ba<sup>2+</sup> ions sites, leading to the creation of Ba and oxygen vacancies to maintain charge neutrality. Structural analyses, including X-ray diffraction (XRD), FT-IR spectroscopy, FE-SEM, and Raman spectroscopy, provided insights into the compositional and structural characteristics of the composites. A structural phase transition from tetragonal to orthorhombic was observed in Gd-modified BaTiO<sub>3</sub>, with coexisting phase noted in (Gd/Ba)TiO<sub>3</sub> samples. SEM analysis revealed reduced particle size and particle shape morphology with increasing Gd content. Photoluminescence (PL) confirmed the impact of the immersion of Gd ions on the BaTiO<sub>3</sub>. Dielectric properties were examined across varying frequencies (100 Hz to 120 MHz) and temperatures (30°C to 500°C), showing a decrease in dielectric constant with increasing Gd content and frequency. This study offers an effective modulation of electronic and dielectric properties through the controlled incorporation of gadolinium in BaTiO<sub>3</sub> material, which offers valuable insights for the development of advanced functional materials tailored for various technological applications.
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DOI: 10.21203/rs.3.rs-4775267/v1
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