In this work, two series of glasses, i.e. (68-x) CuO – xV2O5 – 32TeO2 (x = 0–68 mol%, Te32 series) and (35-x) CuO – xV2O5 – 65TeO2 (x = 0–35 mol%, Te65 series), were synthesized by the melt-quenching method and subjected to physical, thermal and electrical characterization. Their vitreous nature was confirmed by X-Ray diffraction and differential scanning calorimetry, while their structural units were determined by Raman spectroscopy. CuO substitution by V2O5 led to a decrease in density and glass-transition temperature, together with a conductivity increase. Conduction mechanism was interpreted as mainly due to small polaron hopping from the lower (V4+) to the higher (V5+) vanadium valence states. Te32 glasses, possessing the highest electronic conductivities (ranging from 2 E−4 to 5 E−7 Ω−1 cm−1), were investigated by the Electron Paramagnetic Resonance technique, in order to more deeply analyze their structure-conductivity correlation. Particularly, the observed signals were determined to consist in a superposition of a first line due to paramagnetic Cu2+ ions and a second line due to exchange-coupled CuO clusters. Differences in the spectra were determined between samples with higher (i.e. 20-30 mol%) Cu2+ concentrations and samples with lower Cu2+ concentrations, suggesting they are located in different local environments. Finally, it was found that the Cu2+ ions are not involved in the process of electron transfer.

Synthesis and characterization of (68-x) CuO – xV2O5 – 32TeO2 (x = 0–68 mol%) and (35-x) CuO – xV2O5 – 65TeO2 (x = 0–35 mol%) glasses: Conduction mechanism, structure and EPR study / Mugoni, C.; Rosa, R.; Giovanardi, R.; Affatigato, M.; Gualtieri, M. L.; Siligardi, C.; Andronenko, S. I.; Misra, S. K.. - In: MATERIALS CHEMISTRY AND PHYSICS. - ISSN 0254-0584. - 266:(2021), pp. 124488-124489. [10.1016/j.matchemphys.2021.124488]

Synthesis and characterization of (68-x) CuO – xV2O5 – 32TeO2 (x = 0–68 mol%) and (35-x) CuO – xV2O5 – 65TeO2 (x = 0–35 mol%) glasses: Conduction mechanism, structure and EPR study

Mugoni C.;Rosa R.;Giovanardi R.;Affatigato M.;Gualtieri M. L.;Siligardi C.;
2021

Abstract

In this work, two series of glasses, i.e. (68-x) CuO – xV2O5 – 32TeO2 (x = 0–68 mol%, Te32 series) and (35-x) CuO – xV2O5 – 65TeO2 (x = 0–35 mol%, Te65 series), were synthesized by the melt-quenching method and subjected to physical, thermal and electrical characterization. Their vitreous nature was confirmed by X-Ray diffraction and differential scanning calorimetry, while their structural units were determined by Raman spectroscopy. CuO substitution by V2O5 led to a decrease in density and glass-transition temperature, together with a conductivity increase. Conduction mechanism was interpreted as mainly due to small polaron hopping from the lower (V4+) to the higher (V5+) vanadium valence states. Te32 glasses, possessing the highest electronic conductivities (ranging from 2 E−4 to 5 E−7 Ω−1 cm−1), were investigated by the Electron Paramagnetic Resonance technique, in order to more deeply analyze their structure-conductivity correlation. Particularly, the observed signals were determined to consist in a superposition of a first line due to paramagnetic Cu2+ ions and a second line due to exchange-coupled CuO clusters. Differences in the spectra were determined between samples with higher (i.e. 20-30 mol%) Cu2+ concentrations and samples with lower Cu2+ concentrations, suggesting they are located in different local environments. Finally, it was found that the Cu2+ ions are not involved in the process of electron transfer.
2021
266
124488
124489
Synthesis and characterization of (68-x) CuO – xV2O5 – 32TeO2 (x = 0–68 mol%) and (35-x) CuO – xV2O5 – 65TeO2 (x = 0–35 mol%) glasses: Conduction mechanism, structure and EPR study / Mugoni, C.; Rosa, R.; Giovanardi, R.; Affatigato, M.; Gualtieri, M. L.; Siligardi, C.; Andronenko, S. I.; Misra, S. K.. - In: MATERIALS CHEMISTRY AND PHYSICS. - ISSN 0254-0584. - 266:(2021), pp. 124488-124489. [10.1016/j.matchemphys.2021.124488]
Mugoni, C.; Rosa, R.; Giovanardi, R.; Affatigato, M.; Gualtieri, M. L.; Siligardi, C.; Andronenko, S. I.; Misra, S. K.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1248145
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