Spectroscopy of the rare-earth-ion transitions in fluoride glasses

2022 ◽  
pp. 333-399
Author(s):  
Stuart Jackson ◽  
Shigeki Tokita ◽  
Mathew R. Majewski ◽  
Ori Henderson-Sapir ◽  
David J. Ottaway ◽  
...  
2012 ◽  
Vol 184 ◽  
pp. 110-115
Author(s):  
X.P. Wang ◽  
J. Hu ◽  
Zhong Zhuang ◽  
Tao Zhang ◽  
Qian Feng Fang

The relaxation and phase transition behaviors of rare-earth ion substituted fast oxide-ion conductors (La1-xRex)2Mo2O9 (Re=Nd, Gd) were investigated by internal friction (IF) measurement in the temperature range 300 K - 950 K. Three different IF peaks (labeled as PL, PH, and PG, respectively) were observed in the rare-earth ion doped La2Mo2O9 samples. Peak PL corresponds to short diffusion processes of oxygen ions among different oxygen vacancy sites. Peak PH is associated with the static/dynamic disorder transition in oxygen ion distribution. Peak PG is a newly discovered peak embodying phase transition-like characteristics and is suggested to be related to order-disorder transition associated with the rearrangement of La/ Re sub-lattice.


1964 ◽  
Vol 2 (8) ◽  
pp. iv
Author(s):  
J. Verdone ◽  
M. Veyssie ◽  
B. Dreyfus

1961 ◽  
Vol 39 (5) ◽  
pp. 1049-1053 ◽  
Author(s):  
P. Glentworth ◽  
R. H. Betts

It is shown that the rare earth ion Yb3+ is very resistant towards ordinary thermal exchange when it is complexed with the chelating agent EDTA in aqueous solution. However, when the complexed rare earth atom, as the 1.8-h Yb-177, emits a beta-particle, the daughter atom Lu-177 escapes readily from the chelate structure. Nuclear recoil arising from the beta-particle emission is shown not to be the cause of the escape of the daughter atom. It is suggested that the observed lability of the daughter atom is a result of a high degree of chemical reactivity of the chelate ion arising from the sudden change in atomic number of the central metal ion of the chelate structure.


2007 ◽  
Vol 49 (1) ◽  
pp. 91-98 ◽  
Author(s):  
U. V. Valiev ◽  
J. B. Gruber ◽  
D. K. Sardar ◽  
B. Zandi ◽  
I. S. Kachur ◽  
...  

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