The polarized 15 K absorption spectra of Zn2SiO4 doped with Ni2+ consist of three-band systems in the near-infrared (NIR) and visible (VIS) spectral regions centered at 4700, 8500, and 16500 cm-1, respectively. In the tetrahedral approximation they are assigned to the d → d transitions 3T1 → 3T2, 3A2, and 3T1(P), respectively. The spectra are interpreted in terms of a Td →C2v site distortion and analyzed using the angular overlap model. The ligand field parameter 10Dq is 4500 cm-1, and the Racah parameters B and C are 780 and 3630 cm-1, respectively. By the inclusion of spin-orbit coupling in the AOM calculation it is possible to assign the rich fine structure in the origin regions of the 3T1 → 3T2, 3A2 absorptions to Ni2+ ions occupying the two crystallographically inequivalent Zn2+ sites of Zn2SiO4. © 1997 Elsevier Science B.V.

Optical spectroscopy of Ni2+ doped crystals of Zn2SiO4 / Brunold, T. C.; Gude, H. U.; Cavalli, E.. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - 268:5-6(1997), pp. 413-420. [10.1016/S0009-2614(97)00237-6]

Optical spectroscopy of Ni2+ doped crystals of Zn2SiO4

Cavalli E.
1997

Abstract

The polarized 15 K absorption spectra of Zn2SiO4 doped with Ni2+ consist of three-band systems in the near-infrared (NIR) and visible (VIS) spectral regions centered at 4700, 8500, and 16500 cm-1, respectively. In the tetrahedral approximation they are assigned to the d → d transitions 3T1 → 3T2, 3A2, and 3T1(P), respectively. The spectra are interpreted in terms of a Td →C2v site distortion and analyzed using the angular overlap model. The ligand field parameter 10Dq is 4500 cm-1, and the Racah parameters B and C are 780 and 3630 cm-1, respectively. By the inclusion of spin-orbit coupling in the AOM calculation it is possible to assign the rich fine structure in the origin regions of the 3T1 → 3T2, 3A2 absorptions to Ni2+ ions occupying the two crystallographically inequivalent Zn2+ sites of Zn2SiO4. © 1997 Elsevier Science B.V.
Optical spectroscopy of Ni2+ doped crystals of Zn2SiO4 / Brunold, T. C.; Gude, H. U.; Cavalli, E.. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - 268:5-6(1997), pp. 413-420. [10.1016/S0009-2614(97)00237-6]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2894392
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