Polycrystalline BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document} and Bi0.9\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {0.9}}}$\end{document}Gd0.1\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {0.1}}}$\end{document}Fe1−x\documentclass[12pt]{minimal}
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\begin{document}$_{\boldsymbol {1-}\boldsymbol {{x}}}$\end{document}TixO3 (x= 0, 0.01, 0.05 and 0.1) samples were synthesized by solid-state reaction route. Structural, magnetic and ferroelectric properties of these samples were investigated. X-ray powder diffraction (XRD) results confirmed the presence of a significant amount of Bi2\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {2}}}$\end{document}Fe4O9\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {4}}}\textit {O}_{\mathrm {\mathbf {9}}}$\end{document} impurity phase in the undoped BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document} sample. Mössbauer spectroscopy studies corroborated the XRD studies to confirm the presence of impurity phase. We have observed that gadolinium (Gd3+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {3+}}$\end{document}) and titanium (Ti4+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {4+}}$\end{document}) doping, respectively, on Bi3+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {3+}}$\end{document} and Fe3+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {3+}}$\end{document} sites facilitated a significant reduction in the impurity phase formation in BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document}. Interestingly, Gd3+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {3+}}$\end{document}-doping significantly reduced the impurity phase formation as compared to the undoped BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document} sample. This impurity phase formation was further overcome by doping higher (x≥\documentclass[12pt]{minimal}
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\begin{document}$\boldsymbol {\ge } $\end{document} 0.05) amounts of Ti in BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document}. The crystallographic site occupancies of Gd and Ti were confirmed by Rietveld refinement of XRD data, Mössbauer spectroscopy and magnetization measurements. An enhancement in ferromagnetic properties along with moderate ferroelectric properties have been observed after co-doping. There was an increasing trend in remnant polarization (Pr\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {r}}}$\end{document}) with the increase in Ti concentration besides an improvement in the characteristic saturation magnetization. Our results demonstrate that Gd3+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {3+}}$\end{document} and Ti4+\documentclass[12pt]{minimal}
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\begin{document}$^{\boldsymbol {4+}}$\end{document} doping could be used to enhance multifunctional properties of BiFeO3\documentclass[12pt]{minimal}
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\begin{document}$_{\mathrm {\mathbf {3}}}$\end{document} ceramics to enable them as potential material for various devices.