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Commentary  |  Open Access  |  5 Jan 2023

High entropy design: a new pathway to promote the piezoelectricity and dielectric energy storage in perovskite oxides

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Microstructures 2023;3:2023003.
10.20517/microstructures.2022.38 |  © The Author(s) 2023.
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Commentary to publications by Prof. Jun Chen, University of Science and Technology Beijing, E-mail: junchen@ustb.edu.cn (10.1038/s41467-022-30821-7; 10.1016/j.actamat.2022.118115).

Intrinsic polarization is an important property that distinguishes ferroelectric materials from others. Tuning the polarization configuration is crucial for promoting the electric performance, including the piezoelectric and dielectric properties. For example, the traditional strategy of constructing phase boundaries, including morphotropic phase boundaries (MPBs) and polymorphic phase boundaries (PPBs), is usually adopted to tune the polarization configuration with coexisting multiple ferroelectric phases to cause a more flexible polarization configuration than that of a single phase, resulting in higher ferroelectricity or piezoelectricity[1-5]. To enhance the energy storage performance of ferroelectrics, macrodomains with an ordered configuration due to long-range polarization are generally broken by tuning the polarization configuration to nanodomains or polar nanoregions (PNRs)[6-8]. These approaches, however, have limited degrees of freedom in further tuning the polarization configuration and improving electrical performance. “High entropy” is a new materials design strategy developed in the 1980s-1990s, but only recently realized in high-entropy alloys in 2004 by Yeh et al.[9], and was gradually extended into the fields of metal carbides and oxides[10,11]. Its excellent high-entropy effect increases the disorder of a system by forming solid solutions of multi-component elements, effectively controlling various properties benefiting from the entropy-dominated phase stabilization, atomic disorder with lattice distortion, sluggish diffusion kinetics and property synergy from multiple components[12-16]. Recently, Chen’s group proposed a high-entropy strategy to successfully promote piezoelectric and energy storage performance in perovskite oxide ceramics by tuning the polarization configuration [Acta Mater. 236 (2022) 118115 - high entropy piezoelectrics Pb(Ni,Sc,In,Ti,Nb)O3[17]; Nat. Commun. 13 (2022) 3089 - high entropy dielectric (K,Na,Li,Ba,Bi)(Nb,Sc,Hf,Zr,Ta,Sb)O3[18]], opening up new ideas for high-entropy piezoelectrics and high-entropy energy storage materials.

It is well known that different elements have different valence states, ionic radii, electronic configurations, electronegativity and polarizabilities. In recent studies, the high-entropy concept has been tuned to enable various elements, such as Ni2+, Mg2+, Sc3+, Yb3+, In3+, Zr4+, Hf4+, Ti4+, and Nb5+, to simultaneously occupy equivalent lattice sites, such as B-sites, in perovskites to enhance the local polarization fluctuation as much as possible, achieving the effect of increasing entropy[17]. After introducing multiple components, as shown in Figure 1A, large-scale transition regions (green color) that are spread out over the whole area demonstrate the high flexibility of this unique polarization configuration. An almost even distribution of polarization angles (θ) over the whole range of 0-45° can be observed in the statistical results [Figure 1B], breaking the constraints of crystallographic symmetry and promoting the polarization rotation under excitation by an electric field[19]. From another perspective, the unique polarization configuration can be considered as coexisting multiple monoclinic phases with different θ values on the atomic scale, which play a bridge-like role between the polarizations of different phases[20], facilitating the flexible rotation between different phases under electric fields. Benefiting from this unique polarization configuration caused by increasing configuration entropy, an ultrahigh piezoelectric coefficient (d33) of ~1210 pC/N can be achieved in the multi-component perovskite ceramics [Figure 1C].

High entropy design: a new pathway to promote the piezoelectricity and dielectric energy storage in perovskite oxides

Figure 1. (A) Contour map of the distribution of polarization angles (θ). (B) Statistics of the distribution of θ in the range of 0°-45°, extracted from over 30, 000 polarization vectors. (C) Strong correlation between d33 and the number of B-site element types (nB) for a series of PbBO3-based solid solutions. Reproduced with permission from[17], Copyright 2022, Elsevier. (D) Atomic-resolution high-angle annular dark field - scanning transmission electron microscopy (HAADF STEM) polarization vector image along [110]c. (E) Comparison of the recoverable energy storage density, Wrec (efficiency, η ≥ 90%), of (K,Na)NbO3 (KNN)-based high-entropy ceramic with other representative lead-free bulk ceramics with Wrec ≥ 1 J cm-3. Reproduced with permission from[18], Copyright 2022, Nature Publishing Group.

A local diverse polarization configuration can greatly enhance the polarization response rate under electric fields, leading to high Wrec and efficiency η in energy storage capacitors[21]. Chen’s group introduced the high-entropy concept into KNN-based ceramics and designed “local polymorphic distortion” to tune the local diverse polarization configuration with coexisting rhombohedral - orthorhombic - tetragonal - cubic (R-O-T-C) multiphase nanoclusters [Figure 1D][18]. Notably, the cations (Li+, Ba2+, Bi3+, Sc3+, Hf4+, Zr4+, Ta5+, Sb5+) introduced by the high entropy strategy take into account the substitution on A-sites and B-sites in perovskites, greatly enhancing the occupancy disorder and perturbation of the polarization. Meanwhile, the cations are also considered as additives used to tailor the phase transition temperatures TR-O, TO-T, and TT-C to construct room-temperature R-O-T-C multiphase nanoclusters coexisting at the local scale. Compared with the dielectrics with single-phase and coexisting two-phase polarization configuration, the high-entropy sample exhibited smaller and more diverse PNRs with weak correlation embedded in the nonpolar cubic phase, providing higher η and delayed polarization saturation under electric fields. In addition, different types of oxygen octahedral distortions exist in different nanophases, which would introduce coexisting multiple randomly-distributed oxygen octahedral tilts, further breaking the local polarization order. As a result, high-entropy designed KNN-based ceramics with local polymorphic distortion achieved breakthroughs in the ultrahigh Wrec (≥ 10 J cm-3) and ultrahigh η (≥ 90%) for lead-free ceramics for the first time [Figure 1E]. The results demonstrate that high-entropy design opens a new avenue to enhance electrical performance by tuning the polarization configuration.

The multiple components introduced by high entropy can cause significant local compositional disorder and random fields, resulting in flexible and diverse local polarization configurations in both high-entropy piezoelectrics and high-entropy energy storage dielectrics. It has to be mentioned that the various elements introduced by the high-entropy strategy endow the material with more performance control freedom and control methods, rather than a single ferroelectric/piezoelectric performance improvement. We believe that high-entropy design will become an important way to enhance the electrical properties of perovskite materials, enriching the design of material components thanks to the rapid development of machine learning and materials genome engineering.

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The author contributed solely to the article.

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The author declared that there are no conflicts of interest.

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Copyright

© The Author(s) 2023.

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Commentary
Open Access
High entropy design: a new pathway to promote the piezoelectricity and dielectric energy storage in perovskite oxides
Shujun ZhangShujun  Zhang

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Zhang, S. High entropy design: a new pathway to promote the piezoelectricity and dielectric energy storage in perovskite oxides. Microstructures. 2023, 3, 2023003. http://dx.doi.org/10.20517/microstructures.2022.38

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