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Site selective spectroscopy and defect chemistry of CaO
The site selective spectroscopy of CaO:Eu3+, CaO:Er3+, and CaO:Pr3+ has been studied. The Eu3+ doped system has a cubic and an orthorhombic site which vary with concentration in a manner that can be quantitatively described by a simple defect equilibrium model. The Er3+ and Pr3+ spectra do not have...
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Published in: | The Journal of chemical physics 1982-09, Vol.77 (5), p.2322-2329 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The site selective spectroscopy of CaO:Eu3+, CaO:Er3+, and CaO:Pr3+ has been studied. The Eu3+ doped system has a cubic and an orthorhombic site which vary with concentration in a manner that can be quantitatively described by a simple defect equilibrium model. The Er3+ and Pr3+ spectra do not have transitions from the cubic site because electric dipole transitions are forbidden but there are strong transitions from the orthorhombic site. The Pr3+ system exhibits efficient relaxation between levels separated by 4000 cm−1 and efficient up-conversion. Both processes are attributed to the presence of states other than those in the 4f2 electron configuration. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.444151 |