Far Infrared Electronic Transitions in Rare Earth Ions

1970 ◽  
pp. 535-560 ◽  
Author(s):  
Armand Hadni
2008 ◽  
Vol 39-40 ◽  
pp. 61-64 ◽  
Author(s):  
M. Elisa ◽  
Ileana Cristina Vasiliu ◽  
Cristiana Eugenia Ana Grigorescu ◽  
B. Grigoras ◽  
H. Niciu ◽  
...  

A wet non-conventional method for preparing aluminophosphate glasses is presented. Aluminophosphate glasses belonging to the oxide system Li2O-BaO-Al2O3-La2O3-P2O5, doped with rare-earth ions (Pr3+, Er3+, Gd3+, and Yb3+) were obtained. The influence of the doping ions on the optical properties of the phosphate glasses has been investigated in relation with micro-structural and local electronic phenomena The optical behavior of Li2O-BaO-Al2O3-La2O3-P2O5 glasses doped with 3% mol. rare-earth ions has been studied by ultra-violet-visible-near-infra-red (UV-VISNIR) spectroscopy. The transmission spectra revealed electronic transitions between 4f and 6s inner orbital of the rare-earth ions. Structural information via optical phonons was provided by infra-red (IR) absorption spectra in the range 400-4000 cm-1. IR optical phonons are characteristic for the vitreous phosphate network, showing out the glass network-forming role of P2O5. The absorption spectra present the main PO2 and P-O-P symmetrical stretch modes besides P-O-P bend mode, P-OH, P=O, PO3 2-, asymmetrical and symmetrical vibration modes. Fluorescence spectra of the rareearth- doped aluminophosphate glasses, in the visible range, were obtained by laser excitation at 514.5 nm. The fluorescence signals revealed specific electronic transitions, which provide visible and near-infra-red emission. Glasses containing rare-earth ions exhibit luminescence at the following wavelengths: Pr3+ ions at 820 nm and 880 nm, Er3+ ions at 520 nm, 550 nm and 560 nm, Gd3+ ions at 530 nm, 540 nm, 550 nm 820 and 880 nm, Yb3+ions at 530 nm, 540 nm, 550 nm and 980 nm.


1988 ◽  
Vol 151 (4-5) ◽  
pp. 315-317 ◽  
Author(s):  
Shigeru Yamauchi ◽  
Hitoshi Kanno ◽  
Yoshifumi Akama

1960 ◽  
Vol 33 (1) ◽  
pp. 192-193 ◽  
Author(s):  
G. Mandel ◽  
R. P. Bauman ◽  
E. Banks

1964 ◽  
Vol 3 (S1) ◽  
pp. 574
Author(s):  
Armand Hadni ◽  
Xavier Gerbaux ◽  
Guy Morlot ◽  
Pierre Strimer

1970 ◽  
Vol 24 (4) ◽  
pp. 436-445 ◽  
Author(s):  
G. V. Subba Rao ◽  
C. N. R. Rao ◽  
J. R. Ferraro

The electronic and ir spectra of rare earth perovskites of the general formula LnZO3, where Ln is the rare earth ion or yttrium and Z is Cr, Mn, or Fe, have been studied in detail. The results have been discussed in terms of crystallography, magnetic properties, covalency of Ln—O and Z—O bonds, and Goodenough's one electron energy diagrams. In all these compounds the rare earth ions do not markedly affect the electronic transitions of the transition metal ions; the 3 d electrons clearly exhibit localized behavior. Both the electronic and ir spectra of the LnZO3 perovskites are comparable to the spectra of the corresponding transition metal sesquioxides, Z2O3.


1976 ◽  
Vol 16 (6) ◽  
pp. 605-617 ◽  
Author(s):  
G. Villermain-Lecolier ◽  
A. Hadni ◽  
G. Morlot ◽  
P. Strimer ◽  
J.P. Aubry

1971 ◽  
Vol 49 (13) ◽  
pp. 2336-2344 ◽  
Author(s):  
J. A. Koningstein ◽  
P. Grunberg

Additional experimental data are reported on electronic Raman scattering of trivalent lanthanides, making the observation of this effect of the series nearly complete. The bulk of the information now available points to the fact that the intensity of electronic Raman transition is strongest for the rare earth ions in the middle of the series. The most profound differences of polarization features of electronic transitions and phonons is observed in the situation where the lanthanide ions have an odd number of 4f electrons. Antisymmetric scattering tensors play a less important role.


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