Structural, electrical and photoluminescence properties of Er3+-doped SrBi4Ti4O15—Bi4Ti3O12 inter-growth ceramics
Er 3+ -doped SrBi 4 Ti 4 O 15 -Bi 4 Ti 3 O 12 (SBT-BIT- x Er 3+ , x = 0.00, 0.05, 0.10, 0.15 and 0.20) inter-growth ceramics were synthesized by the solid-state reaction method. Structural, electrical and up-conversion properties of SBT-BIT- x Er 3+ were investigated. All samples showed a single pha...
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Published in | Frontiers of materials science Vol. 13; no. 1; pp. 99 - 106 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Beijing
Higher Education Press
01.03.2019
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Er
3+
-doped SrBi
4
Ti
4
O
15
-Bi
4
Ti
3
O
12
(SBT-BIT-
x
Er
3+
,
x
= 0.00, 0.05, 0.10, 0.15 and 0.20) inter-growth ceramics were synthesized by the solid-state reaction method. Structural, electrical and up-conversion properties of SBT-BIT-
x
Er
3+
were investigated. All samples showed a single phase of the orthorhombic structure. Raman spectroscopy indicated that the Er
3+
substitution for Bi
3+
at A sites of the pseudo-perovskite layer increases the lattice distortion of SBT-BIT-
x
Er
3+
ceramics. The substitution of Bi
3+
by Er
3+
leads to a decrease of dielectric loss tanδ and an increase of conductivity activation energy. Piezoelectric constant
d
33
was slightly improved, but dielectric constant was decreased with the Er
3
+ doping. The SBT-BIT-
x
Er
3+
ceramic with
x
= 0.15 exhibits the optimized electrical behavior (
d
33
~17 pC/N, tanδ ~0.83%). Moreover, two bright green (532 and 548 nm) and one red (670 nm) emission bands were observed under the 980 nm excitation. Optimized emission intensity was also obtained when
x
= 0.15 for the SBT-BIT-
x
Er
3+
ceramic. Therefore, this kind of ceramics ought to be promising candidates for multifunctional optoelectronic applications. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 2095-025X 2095-0268 |
DOI: | 10.1007/s11706-019-0454-3 |