2004
DOI: 10.1007/s00269-004-0393-z
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Temperature dependence of the polarized electronic absorption spectra of olivines. Part II?Cobalt-containing olivines

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Cited by 22 publications
(27 citation statements)
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“…These assignments are in good agreement with those reported in earlier works [15][16][17]. Furthermore, spin-forbidden d-d transitions to the other excited terms could be contributing to the absorbance at still higher energies (up to 300 nm) in the near-UV region [17]. However, these bands as well as those in NIR region (900-1600 nm) do not contribute to the absorption in the borders of visible zone and thus, they do not have any optical effect.…”
Section: Optical Spectroscopy (Powders)supporting
confidence: 93%
See 1 more Smart Citation
“…These assignments are in good agreement with those reported in earlier works [15][16][17]. Furthermore, spin-forbidden d-d transitions to the other excited terms could be contributing to the absorbance at still higher energies (up to 300 nm) in the near-UV region [17]. However, these bands as well as those in NIR region (900-1600 nm) do not contribute to the absorption in the borders of visible zone and thus, they do not have any optical effect.…”
Section: Optical Spectroscopy (Powders)supporting
confidence: 93%
“…For the infrared region, the bands centred at around 1300 (M1 sites) and 1560 nm (M2 sites) correspond to the ν 1 spin-allowed transitions to the excited term 4 T 2 (F). These assignments are in good agreement with those reported in earlier works [15][16][17]. Furthermore, spin-forbidden d-d transitions to the other excited terms could be contributing to the absorbance at still higher energies (up to 300 nm) in the near-UV region [17].…”
Section: Optical Spectroscopy (Powders)supporting
confidence: 88%
“…The red-shift is likely due to the thermal expansion as the energy separation between the t 2g and e g orbitals is inversely proportional to the fifth power of the metal-ligand distance (Burns, 1993). Intensity variations of CF bands with temperature reported in the literature show a less regular behavior (Shankland et al, 1979;Fukao et al, 1968;Goncharov et al, 2008;Ullrich et al, 2002Ullrich et al, , 2004Thomas et al, 2012;Taran et al, 1994), but often may be understood in terms of temperature-induced changes in the CF symmetry (Taran and Langer, 2001) lifting the Laporte selection rule, which impedes electron transfer among the same parity states (e.g. d-d transitions).…”
Section: Gpamentioning
confidence: 94%
“…These assignments were in good agreement with reported earlier works. 32,13,33 Once again, the optical spectra of all Mg 2−x Co x SiO 4 pigments indicate that their violet color is due to the d-d transitions within Co 2+ ions in the forsterite octahedral sites and results from absorption over all visible spectra except the violet region around 400-450 nm. The Co 2+ preference for olivine M1 sites confirmed by several works based on X-ray structure refinement of a synthetic Mg-Co 2+ olivine (see, Ghose and Wan 34 ; Bostrom 35 ), is less evident from crystal field spectra of Mg 2−x Co x SiO 4 .…”
Section: Microstructure Of Forsterite and Pigment Samplesmentioning
confidence: 98%