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Dielectric dispersion and impedance spectroscopy of NiO doped Li2SO4–MgO–P2O5 glass system

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Abstract Li2SO4–MgO–P2O5 glasses mixed with a varied quantity of NiO were prepared. Detailed spectroscopic investigations (viz., OA, IR and Raman) spectra were carried out. Optical absorption spectral results indicated that… Click to show full abstract

Abstract Li2SO4–MgO–P2O5 glasses mixed with a varied quantity of NiO were prepared. Detailed spectroscopic investigations (viz., OA, IR and Raman) spectra were carried out. Optical absorption spectral results indicated that Ni2+ ions in the glass network reside in octahedral (Oh) as well as tetrahedral (Td) sites; these results have also pointed out the growing concentration of Ni2+ ions in Oh sites as NiO concentration is increased up to 0.8 mol%. Results of infrared and Raman spectral studies indicated increased internal chaos in the sulpho-phosphate glass network with an increase of NiO concentration up to 0.8 mol%. Values of dielectric permittivity (both real and imaginary components), a.c. conductivity, σac, are observed to be gradually increasing with NiO content in the concentration range 0–0.8 mol%. Electric moduli spectra have exhibited dipolar relaxation effects and the dipolar relaxation time τ estimated from these spectra exhibited a decreasing trend with the raise of NiO quantity up to 0.8 mol%. The complexes of octahedral Ni2+ ions with oxygen ions are predicted to be the possible dipoles responsible for the dipolar effects. Variation of σac with NiO content exhibited an increasing trend up to 0.8 mol%. Quantitative analysis of this observation indicated ionic contribution to σac is dominant in the glasses containing small quantities of NiO ( 0.8 mol%) polaronic contribution to the conductivity seems to be present. Overall, the results of dielectric properties of studied glass system indicted that the glass with low quantities of NiO (

Keywords: glass; mgo p2o5; li2so4 mgo; glass system; spectroscopy

Journal Title: Journal of Alloys and Compounds
Year Published: 2020

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