Vrl. Constantino et al., PHOTOLUMINESCENCE STUDY OF LAYERED NIOBATES INTERCALATED WITH EU3+ IONS, Journal of alloys and compounds, 278(1-2), 1998, pp. 142-148
In the present work the lamellar phases of composition K4Nb6O17, KNb3O
8 and KCa2Nb3O10 were used as precursors to prepare new compounds thro
ugh the potassium exchange reaction with Eu3+ ion via a soft chemistry
route. The precursors show absorption bands in the UV range and KNb3O
8 exhibits blue emission at room and liquid nitrogen temperature, whil
e K4Nb6O17 presents emission spectra only at low temperature. The aim
of this work is to investigate the photoluminescence properties of Eu3
+-exchanged layered oxides through the analysis of their excitation an
d emission spectra. The compounds show the general formulae Eux/3K4-xN
b6O17. zH(2)O (1), Eux/3K1-xNb3O8. zH(2)O (2) and Eux/3K1-xCa2Nb3O10.z
H(2)O (3) and were characterized by X-ray diffraction and europium and
potassium analyses. The emission spectra of the samples recorded at 2
98 and 77 K temperatures showed transitions between the D-5(0) and F-7
(J) (J=0-4) levels that indicate the presence of Eu3+ ions in C-nv sit
e symmetry. It was observed for systems (2) and (3) that the D-5(0)-->
F-7(0) transition does not split, which indicates that the Eu3+ ion is
found only in one site symmetry. On the other hand, the system (1) sp
ectra indicated the presence of the rare earth ions in two different s
ite symmetries. Since the precursor K4Nb6O17 has two crystallographica
lly distinct interlayer regions, we suggest that the K+ ion is replace
d by the Eu3+ ion in the two interlamellar regions of the material (1)
. In the case of the system (2), two types of emission spectra were ob
served at room temperature: blue luminescence due to matrix excitation
and red emission due to the direct excitation of the Eu3+ ion. The va
lues of the Omega(lambda) (lambda = 2, 4) experimental intensity param
eters for these three lamellar compounds suggest that the short distan
ce effects are not dominant. (C) 1998 Elsevier Science S.A. All rights
reserved.