Lanthanide level location in transition metal complex compounds

被引:168
作者
Dorenbos, P. [1 ]
Krumpel, A. H. [1 ]
van der Kolk, E. [1 ]
Boutinaud, P. [2 ,3 ]
Bettinelli, M. [4 ]
Cavalli, E. [5 ]
机构
[1] Delft Univ Technol, Fac Sci Appl, NL-2629 JB Delft, Netherlands
[2] Univ Clermont Ferrand, Lab Mat Inorgan, UMR 6002, Aubiere, France
[3] ENSCCF, Aubiere, France
[4] Univ Verona, Lab Solid State Chem, INSTN, UdR Verona, I-37100 Verona, Italy
[5] Univ Parma, Dipartimento Chim Gen & Inorgan, I-43100 Parma, Italy
关键词
Transition metal compounds; Charge transfer; Lanthanide levels; INTERVALENCE CHARGE-TRANSFER; EXCITED-STATE DYNAMICS; LUMINESCENCE; EMISSION; CRYSTALS; ENERGY; PR3+; PHOSPHORS; EU3+;
D O I
10.1016/j.optmat.2010.02.021
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
We will provide a method to place the levels of all trivalent lanthanides with respect to the top of the valence band and bottom of the conduction band in oxides containing transition metal complexes. The method will be applied to CaTiO(3), YVO(4), LaVO(4), CaNb(2)O(6), YNbO(4), CaWO(4), YTaO(4), and LaTaO(4), but in principle can be applied to any oxide containing transition metal complexes with lanthanide dopants on either rare earth or alkaline earth sites. Crucial to place the energy levels is the energy for intervalence charge transfer between a lanthanide (Fr(3+) and Tb(3+)) and a transition metal ion (Ti(4+), V(5+), Nb(5+), Mo(6+), Ta(5+), W(6+)) that can be observed in luminescence excitation spectra. The quenching of Pr(3+) emission from the (3)P(0) state and of Tb(3+) emission from the (5)D(3) and (5)D(4) states provides complementary information. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1681 / 1685
页数:5
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