News Release

Unconventional piezoelectricity in ferroelectric hafnia

Peer-Reviewed Publication

Helmholtz-Zentrum Berlin für Materialien und Energie

Unconventional piezoelectricity in ferroelectric hafnia

image: 

The effect: polarisation and electric field are pointing in the same direction. With positive d33, the sample expands,  whereas the material is contracting when d33 is negative.

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Credit: Laura Canil

Hafnium oxide thin films are a fascinating class of materials with robust ferroelectric properties in the nanometre range. While the ferroelectric behaviour is extensively studied, results on piezoelectric effects have so far remained mysterious. A new study now shows that the piezoelectricity in ferroelectric Hf0.5Zr0.5O2 thin films can be dynamically changed by electric field cycling. Another ground-breaking result is a possible occurrence of an intrinsic non-piezoelectric ferroelectric compound. These unconventional features in hafnia offer new options for use in microelectronics and information technology.

 

Since 2011, it has been known that certain hafnium oxides, are ferroelectric, that is, they possess a spontaneous electric polarization whose direction can be switched in the opposite one by applying an external electric field.  All ferroelectrics exhibit piezoelectricity and, most often, a positive longitudinal piezoelectric coefficient (d33). This means that the crystal expands if the applied electric field is in the same direction than the electrical polarization. However, for hafnia, studies have shown contradictory results, with different hafnia films expanding or contracting in the same experimental conditions. Moreover, the ferroelectric polarization can apparently switch against the electrical field, which was named “anomalous” switching.

Unconventional behaviour investigated

An international collaboration led by Prof. Dr. Catherine Dubourdieu, HZB, has now elucidated for the first time some aspects of these mysterious results and discovered an unconventional behaviour in hafnia. They investigated Hf0.5Zr0.5O2 (HZO) capacitors using piezoresponse force microscopy (PFM): a conductive needle scans the sample surface under a small electrical voltage and measures the local piezoelectric response.

Switching piezoelectricity

Their study revealed that piezoelectricity in HZO is not an invariable parameter but is a dynamic entity that can be changed, in the very same material, by an external stimulus such as electrical cycling. The ferroelectric HZO capacitors undergo a complete uniform inversion of the piezoelectric d33 coefficient sign, from positive to negative, upon electric field cycling. Every single location of the ferroelectric capacitor undergoes such a change passing through zero local piezoelectricity upon suitable number of ac cycles.

New option: ferroelectric materials without piezoelectricity

Density functional theory calculations suggest that the positive d33 in the initial state is due to a metastable polar orthorhombic phase that gradually evolves, under ac cycling, towards the fully developed stable polar phase with negative d33. The DFT calculations not only suggest a mechanism for the d33 sign inversion but also predict a groundbreaking result: a possible occurrence of an intrinsic non-piezoelectric ferroelectric compound, which is observed experimentally.

New applications

"For the first time, we have ben able to experimentally observe a sign inversion of the piezoelectric effect in the whole area of a capacitor in these Hafnia Zirconia ferroelectrics under applied ac electric field,” Catherine Dubourdieu states. This discovery has enormous potential for technological applications. “As the piezoelectricity in these materials can be dynamically changed and even nullified while the polarisation remains robust, we see fantastic prospects for developing ferroelectric HfO2-based devices with electromechanical functionalities. Moreover, on a fundamental standpoint, the possibility of a non-piezoelectric ferroelectric compound would revolutionize our vision of ferroelectricity." says Catherine Dubourdieu.


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