advances in condensed matter physics
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Hindawi Publishing CorporationAdvances in Condensed Matter PhysicsVolume 2013, Article ID 296419, 5 pageshttp://dx.doi.org/10.1155/2013/296419
Research ArticleStructural Disorder in the Key Lead-Free Piezoelectric Materials,Kš„
Na1āš„
NbO3 and (1 ā š„)Na0.5Bi0.5TiO3 + š„BaTiO3
Jason Schiemer,1,2 Ray Withers,1 Yun Liu,1 Yiping Guo,1 Zhiguo Yi,1 and Jian Wang1
1 Research School of Chemistry, Australian National University, Science Road, Acton, ACT 0200, Australia2 Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EQ, UK
Correspondence should be addressed to Jason Schiemer; [email protected]
Received 25 October 2013; Accepted 17 November 2013
Academic Editor: Danyang Wang
Copyright Ā© 2013 Jason Schiemer et al.This is an open access article distributed under the Creative Commons Attribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Using electron diffraction, trends in the local structural behaviour of the Kš„Na1āš„
NbO3(KNN x) and the (1 ā š„)Na
0.5Bi0.5TiO3+
š„BaTiO3(NBT-(š„)BT) systems are investigated. In KNN, electron diffraction shows a single plane of diffuse intensity perpendicular
to [010] across the entire phase diagram, indicating the existence of ferroelectric disorder along this axis. An additional characteristicpattern of diffuse scattering is also observed, involving rods of diffuse intensity running along the [100]p
ā and [001]pā directions
of the perovskite substructure and indicative of octahedral tilt disorder about these axes. Similarly, in the NBT-xBT system,rods of diffuse intensity running along the āØ100ā©p
ā directions of the perovskite substructure are observed, again indicatingoctahedral tilt disorder. Ferroelectric-like disorder is also observed in highly BT doped samples, and a continuous change fromthe ārhombohedralā structure of NBT to the ātetragonalā structure of NBT-12BT is seen from characteristic variation in observedsuperstructure reflections. A crystal chemical rationalisation of these results is performed, and the implications for structure andproperties are discussed.
1. Introduction
Kš„Na1āš„
NbO3(KNN x) became known as a promising
lead-free piezoelectric ceramic system when relatively highpiezoelectric coefficients (up to ā¼300 pC/N) along with Curietemperatures of up to 400āC were reported by Saito et al.in 2004 [1]. (1 ā š„)Na
0.5Bi0.5TiO3+ xBaTiO
3(NBT-xBT) is
similarly high performing. Its raw piezoelectric performanceis not as high as in KNN, ā¼160 pm/V [2], but it can displayhuge electrostrictive strains, up to 0.48% [3], which showpromise for electrostrictive actuators with zero strain, as longas they are designed to account for their nonlinear response.These materials are among the few lead-free piezoelectricmaterials that can compete with lead-based materials in spe-cialized applications. Due to their performance, the structureof materials such as KNN and NBT-BT is of considerableinterest in order to establish structure-property relationshipsand to engineer improvements.
At room temperature in the KNN system, there is longrange ferroelectric order in the plane perpendicular to aparticular parent perovskite āØ001ā©p direction (usually taken
to be the [010]p direction in KNN). As long range ferroelec-tric order is established along both the [100]p and [001]pdirections, the direction of the spontaneous polarization isthen along a parent perovskite āØ101ā©p direction, in the caseof the end-member KNbO
3, and it might be expected to
remain largely unchanged across the KNN phase diagramunless there is an unexpectedly strong coupling betweenferroelectric ordering and octahedral tilt rotation. There is apattern of octahedral tilting induced by the introduction ofthe smaller Na+ ions into the perovskite š“ sites of the origi-nally unrotated, Amm2, KNbO
3structure type. According to
the current phase diagram [4], the onset of b+ tilting does notoccur until a value of š„ = 0.4. š+ tilting is then reported tooccur from š„ = 0.4 to 0.2, below which šā, š+, and šā tiltsare reported. The nature of the local structure has not beenclosely examined, as previous investigations involve powderdiffraction using neutrons [5] andX-rays [4, 6], which are notvery sensitive to short range order.
NBT-BT initially appears simpler than that in KNN.The end member, NBT, is rhombohedral, with ferroelec-tricity along a particular [111]p direction. Above ā¼7% BT
2 Advances in Condensed Matter Physics
doping, the rhombohedral NBT structure transitions toa metrically tetragonal state when observed with powderdiffraction methods, while a pseudocubic state exists in theāmorphotropic phase boundaryā between these two phases.Additionally, there are electric field dependent phase transi-tions in this system at 7% BT doping [7], from pseudocubicto metrically tetragonal, which are irreversible.
Very few electron diffraction or diffuse scattering investi-gations have been performed on these systems. This reportseeks to examine disorder present in these materials, inparticular, the correlations between the two system andthe effects of this disorder on structure determination andproperties.
2. Materials and Methods
Synthesis of KNN x was performed for samples of com-position š„ = 0.15, 0.21, 0.35, 0.46, and 0.75. This wasby solid-state reaction for š„ = 0.15, 0.21, 0.35, and 0.75.Starting reagents were K
2CO3, Na2CO3, and Nb
2O5. Mixing
and homogenising of reagents were performed in a planetaryball mill, using yttrium stabilised zirconia balls in polymerictanks. The reagents were ball-milled in stoichiometric ratiosfor 12 h under acetone followed by calcining at 900āC for5 h to drive off carbon dioxide and begin the reaction toform KNN. Ball milling and calcination at 900āC werethen repeated for homogeneity and complete decomposition.Finally, the powders were ball-milled again for 12 h andpressed into 20mmpellets at 175MPa in a uniaxial steel press,followed by sintering in a bed of loose powder on Pt foil, inlidded alumina crucibles for 4 h in the range of 1030āC forKNN, š„ = 0.15 to 1110āC for KNN, š„ = 0.75. The š„ = 0.46sample was prepared by sol-gel synthesis as described in [8].
NBT-xBT ceramics of composition š„ = 0, 0.04, 0.06, 0.07,0.08, 0.10, and 0.12 were synthesized by solid-state reaction.These samples were from the same batch as described in [9].Starting reagents were Na
2CO3, Bi2O3, BaCO
3, and nano-
TiO2
(ā¼20 nm). These were ball-milled for 5 h in ethanol,followed by calcination at 800āC for 2 h.The calcined powderwas ball-milled again for 2 h and dried, followed by theaddition of poly(vinylalcohol) binder. This powder was thenpressed into pellets with a diameter of 13mm in a uniaxialsteel press at 200MPa. Finally, these pellets were sintered at1150āC for 2 h in a covered alumina crucible.
The purity and apparent metric symmetry of the resul-tant ceramic samples were investigated by X-ray powderdiffraction (SiemensD-5000, Cu radiation andGuinier-Haggcamera, CuK
š¼1radiation), and all samples were found to
be pure and free from secondary phases. The Guinier-Haggpatterns collected on the solid-state synthesized KNN sam-ples are shown in Figure 1, below, while the relevant patternsfor the KNN 46 sample and the NBT-xBT samples arereported in [8, 9] respectively. Electron diffraction patterns(EDPs) were obtained using Philips EM 430 and Philips CM30 Transmission Electron Microscopes (TEMs) operating at300 kV on crushed sample powders dispersed onto holeycarbon coated, copper grids.
0 20 40 60 80
2š (deg)
KNN 15
KNN 21
KNN 35
KNN 75
001pc 011pc 111pc 112pc012pc002pc
Figure 1: Guinier-Hagg X-ray diffraction patterns of solid-statereacted KNN, showing only the expected perovskite-related peaks.The subscript āpcā indicates pseudocubic indexing.
3. Results and Discussion
3.1. KNN Average Structure. In all discussions on EDPs, asubscript p denotes that the indexing is with respect to aparent perovskite subcell. EDPs of KNN as a function ofcomposition are shown in Figures 2(a) and 2(b). We startwith the unrotated, high š„ samples and then consider theoctahedrally rotated phases that occur when š„ is reduced.With š„ = 0.75 (see Figure 2(a)), there are no additionalsuperstructure reflections, and the structure appears to beAmm2, as is well known for KNbO
3.There are, however, faint
diffuse features, which will be discussed subsequently. Fromš„ = 0.46 down to š„ = 0.21, ašŗpĀ±1/2(101)p type spot occurs,with the intensity of this spot increasing with decreasingpotassium content. A sharp šŗp Ā± 1/2(111)p spot appears inš„ = 0.15 (Figure 2(b)) in addition tošŗpĀ±1/2(101)p. A diffusefeature exists at šŗp Ā± 1/2(111)p in all patterns from š„ = 0.46to š„ = 0.21. Weak spots associated with a doubled š axis canbe seen in the š„ = 0.15.
3.2. NBT-BT Average Structure. EDPs of NBT-BT as a func-tion of BT dopant are shown in Figures 2(a) and 2(b).We startwith the ārhombohedralā NBT end member and examinethe superstructure reflections as BT is introduced. Previousrefinements suggest that the structure remains rhombohedralwith š„ < 0.06, going pseudocubic at 0.06 < 0.07 andtetragonal for š„ > 0.07. Examination of the diffractionpatterns does not reproduce these findings.There is, in fact, acontinuous change of intensity between the ārhombohedralāšŗp Ā± 1/2(111)p spot and the ātetragonalā šŗp Ā± 1/2(101)pspot, both of which exist to some degree, even in pureNBT. Increasing the BT content reduces the intensity ofthe ārhombohedralā spot and increases the intensity of theātetragonalā spot, but neither disappears completely. Thewidth of the ātetragonalā peak is also noticeably higher thanthe parent reflections, even in NBT-12BT.
3.3. Diffuse Scattering. In all KNN EDPs, a single planeof diffuse scattering is observed perpendicular to [010],as expected from being in the singly disordered ferro-electric (orthorhombic) state [11] (chevron-headed arrowswith dashed tails in Figures 2(a) and 2(b)). This diffusescattering indicates ordered ferroelectricity in the 101 plane,
Advances in Condensed Matter Physics 3
010p
ā103p
102
(a)
010p
ā103p
102132
(b)
Figure 2: Electron diffraction patterns along a ā3, 0, ā1p axis in KNN x with (a) š„ = 0.75 and (b) š„ = 0.15.
001p
310p
(a)
001p
310p
(b)
Figure 3: Electron diffraction patterns along a 301p axis in NBT-xBT with (a) š„ = 0 and (b) š„ = 0.12.
with columnar disorder along [010]. In NBT, no ferro-electric diffuse is seen, again, as expected from being thefully ordered ferroelectric (rhombohedral) state. However,examination of the diffraction patterns from NBT-12BT(Figure 3(b)) shows planes of diffuse intensity perpendicu-lar to [111]p, indicating ferroelectric disorder along theseaxes (chevron-headed arrows with dashed tails), generatedby the addition of BT. Additionally, šŗp Ā± [1/2, 1/2, š]p
ā-type streaks of diffuse intensity, denoted by chevron-headedarrows with solid tails, are observed from 1/2(111)p to1/2(110)p and to 1/2(011)p at all compositions in KNNand from 1/2(111)p to 1/2(110)p, to 1/2(101)p, and to1/2(011)p in NBT-BT.These one-dimensional rods of diffuseappear both in the plane and as diffuse āspotsā (solid-headed arrows with solid tails) which arise from the Ewaldsphere cutting through one of the rods of diffuse intensity.In KNN, these can be indexed as šŗp Ā± [š, 1/2, 1/2]p
ā oršŗp Ā± [1/2, 1/2, š]p
ā and in NBT-BT as šŗp Ā± [š, 1/2, 1/2]pā
or šŗp Ā± [1/2, 1/2, š]pā or šŗp Ā± [1/2, š, 1/2]p
ā. This effect alsogives rise to apparent āspotsā of the type šŗp Ā± [1/2, 1/2, 0]p
ā
and šŗp Ā± [1/2, 1/2, 1/2]pā, which can be misleading in pat-
terns which show no other evidence that the āreflectionsāoriginate from diffuse rods. In NBT-BT, the continuousmovement of intensity between the ārhombohedralā šŗp Ā±1/2(111)p spot and the ātetragonalā šŗp Ā± 1/2(101)p spot isaccompanied by a continuous diffuse streak between thesespots for all compositions and thešŗpĀ±1/2(101)p spot remainsdiffuse and anisotropic, even when relatively strong. Denoyeret al. [12] observed streaking of the type šŗp Ā± [š, 1/2, 1/2]p
ā
in NaNbO3near a phase transition at 641 K and assigned it to
oxygens in the structure. Indeed, the directions and locationsof these streaks in bothKNNandNBT-BT suggest octahedraltilt twin disorder along their axes, as does the absence of evenharmonics of the type šŗp Ā± [1, 1, 2š]p
ā
/šŗp Ā± [2š, 1, 1]pā.
In KNN, the diffuse rods are clearer for lower sodiumcompositions. This is unsurprising, as KNbO
3is untilted,
4 Advances in Condensed Matter Physics
Figure 4: Tilt twin region in NBT/NBT-BT showing two rhom-bohedral twins with different polarization directions meeting in atetragonal tilt twin region, as shown by the dashed box. Modifiedversion reproduced with permission from [10].
while NaNbO3is highly tilted, and is due to the fact that
tilts increase š“ site valence and decrease šµ site valence, andsodium is much smaller than potassium. Disorder in thetilts gives them zero amplitude in refinements of the averagestructure.The continuous nature of the changes of tilt inKNNimplies that there are no phase boundaries with ferroelectricpolarization rotation, which are known to lead to temperatureindependent phase boundaries with enhanced properties.Similarly in NBT, tilt disorder is likely to stem from thesignificant ionic site size requirement mismatch between aBiIII and a NaI ion. Performing bond valence sums on theICSD structure, the valence for Na is found to be 0.12 v.u.high and Bi is found to be 0.60 v.u. low. Ordering of theseions may be expected, but this is likely to be frustrated bykinetic and ferroelectric requirements, and no superstructureis observed. Tilt twin disorder of the kind shown in Figure 4may be occurring, with the larger twin boundary sites morelikely to contain the sodium ion. The final question in NBT-BT is with regard to what occurs when BT is added to NBT,which is effectively the addition of BaII to the structure, whichrequires amuch larger ionic cavity thanNaI or BiIII.This effectis likely to force the Ba ions to occupy twin boundary regions,and it appears that the twin boundary region is able to expandto a multiple unit cell thickness, due to the driving forceof accommodating Ba, creating layers of tetragonal BT-likematerial between twins of rhombohedral NBT-like material.
If the dopant concentration is sufficiently high, thenthis twin boundary region will become the ābulkā and therhombohedral ābulkā region will become the twin boundary,giving a continuous intensity shift from rhombohedral-likereflections to tetragonal-like reflections, as is experimentallyobserved. This has been observed directly in NBT-6BT with3% KNN [13], with polar nanoregions of R3c and P4bmstructure reported.Thismixing of structures induces disorderin the ferroelectric direction observed from diffuse scattering
and may lead to the reported antiferroelectric behaviour andgiant strain in NBT-BT.
4. Conclusions
In this report we have examined the local structure anddisorder in NBT-BT and KNN. This investigation has showna single, undisturbed ferroelectric plane of diffuse scatteringin all compositions of KNN. Additionally, KNN showsdisordered octahedral tilting at all compositions due to themismatch in size between K and Na atoms. This disorderedtilting behaviour locks into some order at the composi-tion dependent tilt transitions, but no polarisation rotationoccurs.
NBT-BT is shown to also have octahedral tilt disorderat all compositions, but ferroelectric disorder only occurswith BT doping. Continuous transfer of intensity from theārhombohedralāšŗp Ā± 1/2(111)p spot to the ātetragonalā šŗp Ā±1/2(101)p spot with increasing BT content is explained asan expansion of the stacking fault boundary regions in thematerial due to the ionic size of Ba. This explanation alsogives a reason for observed ferroelectric disorder in NBT-12BT and may supply information about the origins of highelectrostrictive response and antiferroelectric behaviour inNBT-BT.
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