Issue 16, 2015

Revealing the role of cationic displacement in potassium–sodium niobate lead-free piezoceramics by adding W6+ ions

Abstract

The effect of the structural modifications induced by the replacement of the B sites with W6+ ions in (K0.44Na0.52Li0.04)[(Nb0.86Ta0.10Sb0.04)1−xW5x/6]O3 lead free ceramics is investigated. Here we show the coexistence between a tetragonal symmetry (T) and an orthorhombic symmetry (O) in the perovskite structure, which is tuned by varying the doping level. In addition, this polymorphic behaviour is accompanied by the appearance of a secondary phase, which can be detected through XRD and Raman results. A correlation between the presence of both structural features and the W6+ content has been evaluated, and therefore this lead free system reveals a transition from a normal ferroelectric to a ‘relaxor-like’ ferroelectric due to the cation disorder in the perovskite-structure in doped samples. A large diffusivity value (γ) has been attained when the x value reached 0.05 owing to the involved O–T polymorphic phase, as well as due to the appearance of a secondary phase. The experimental proof makes clear that the role of the secondary phase is to capture the alkali ions of the (KNa)NbO3-based system, provoking a cation disorder in the perovskite-structure matrix. The significance of this work lies in evaluating whether such a material can benefit the understanding of (KNa)NbO3-based ceramics and the expansion of their application range.

Graphical abstract: Revealing the role of cationic displacement in potassium–sodium niobate lead-free piezoceramics by adding W6+ ions

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2014
Accepted
17 Mar 2015
First published
18 Mar 2015

J. Mater. Chem. C, 2015,3, 4168-4178

Author version available

Revealing the role of cationic displacement in potassium–sodium niobate lead-free piezoceramics by adding W6+ ions

L. Ramajo, M. Castro, A. del Campo, J. F. Fernandez and F. Rubio-Marcos, J. Mater. Chem. C, 2015, 3, 4168 DOI: 10.1039/C4TC02908A

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