EPR and optical absorption studies of Cr3+ ions in alkaline earth alumino borate glasses
Electron paramagnetic resonance (EPR) and optical absorption spectra of Cr3+ ions in Calcium alumino borate (CaAB) glasses have been studied. The EPR spectra exhibit weak resonance signal at g ≈ 4.50 and intense resonance signal at g ≈ 1.98. A sharp resonance signal at g ≈ 1.97 was also observed at...
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Veröffentlicht in: | Journal of materials science 2006-04, Vol.41 (7), p.2045-2053 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Electron paramagnetic resonance (EPR) and optical absorption spectra of Cr3+ ions in Calcium alumino borate (CaAB) glasses have been studied. The EPR spectra exhibit weak resonance signal at g ≈ 4.50 and intense resonance signal at g ≈ 1.98. A sharp resonance signal at g ≈ 1.97 was also observed at lower concentrations of chromium. The concentration dependence of the linewidth of the resonance signal at g ≈ 1.98 suggests the formation of Cr3+ ion clusters by magnetic superexchange interactions. The temperature dependence of the peak to peak intensity and the linewidth of the resonance signal at g ≈ 1.98 suggests that the exchange interactions between Cr3+ ions in the present sample were antiferromagnetic in nature with Néel temperature, TN = 233 K. From the number of spins participating in the resonance at g ≈ 1.98, the paramagnetic susceptibility (χ) was calculated at different temperatures (233–295 K). A plot of 1/χ and T was found to obey Curie-Weiss law with negative Curie temperature. By measuring the relative intensities of the resonance signal at g ≈ 1.98, at different temperatures, the value of antiferromagnetic coupling constant (J) has been estimated. The optical absorption spectrum of chromium doped CaAB glass exhibits four bands, characteristic of Cr3+ ions, in nearly octahedral symmetry. From the band positions, the crystal field splitting parameter, Dq and the Racah interelectronic repulsion parameters, B and C were evaluated. The optical band gap (Eopt) and the Urbach energy (ΔE) were calculated from the ultraviolet absorption edges. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-006-0889-7 |