Expanding the limits of ferroelectrics

This handy property mostly arises from distortions within the ferroelectrics’ crystal structure. These, in turn, create tiny electric dipoles, whose polarities, plus and minus, can be reversed by a subtle, locally applied electric field. This way, it is possible to manipulate two distinct polarisation states within the material — similar to the 0 and 1 states of a “bit” in magnetic memory devices. “This means that one can ‘write’ on the material with an electric field and use it to store information,” explains Gattinoni.

However, this adaptable polarisation remains robust only to a certain critical thinness of the material, which is a limiting factor for the miniaturisation of electronic systems. Gattinoni’s work provides insight into why the polarisation is lost and how this could be overcome — specifically, how ferroelectric materials could be engineered to sustain stable polarisation even in very thin nano-scale films.

Pinpointing the trouble in thin films

To that end, Gattinoni and her colleagues performed density functional theory (DFT) calculations using the “Piz Daint” supercomputer at CSCS. The scientists probed very thin films, above and below a thinness of only 7 unit cells, and compared the results to experiments performed by their collaborators at the lab for ferroic materials at ETH on a film of lead titanate (PbTiO3) — a prototypical ferroelectric material — placed on a strontium ruthenate metal waver. The combined results offer insights into the cause of the suppressed polarisation.

Two known phenomena contribute to this polarisation loss. One is the so-called depolarising field, which arises from opposite charges on the opposite surfaces of the material — a natural consequence of its dipole moment. These charges create an electric field that is contrary to the direction of the ferroelectric polarisation. The thinner the film, the closer these opposite charges come to one other, and, consequently, the stronger this destructive depolarising field becomes. The second phenomenon arises from the instability of the surface charges, per se. “In practice, the system has to find a way to compensate the surface charges in order to maintain the ferroelectric properties,” explains Gattinoni. Her DFT calculations indicate a way to achieve this even in thin films.

Thinking thinner

Gattinoni found that, contrary to previous suppositions, the chemical bonding at the interface between the ferroelectric and the underlying metal — in this case a strontium ruthenate layer — does not have a major influence on maintaining polarisation. Instead, the electronic structure and therefore the electrostatic properties of the ferroelectric and the metal layer play the dominant role in the system. “This means that for controlling the polarisation stability, researchers need to engineer the electrostatic properties, rather than focus on the chemical bonding,” Gattinoni says.

Her calculations also gave indications as to where such modifications would have the highest effect on charge compensation. According to the results, charge transfers at the interface between ferroelectric and metal, which had previously been assumed to be vital, really only play a minor role. In contrast, modifications at the ferroelectrics’ surface proved to be significantly more effective. Such modifications could consist of the introduction of structural defects to create vacancies that can adsorb the charges or of charge-adsorbing molecules in a device’s atmosphere. “Both of these methods can be used to stabilise the polarisation, even in very thin ferroelectric films,” Gattinoni says.

The magical material

Ferroelectrics are also expected to have a big impact on the catalysis of certain important chemical reactions. In this context, Gattinoni recently investigated a material that is, as she says, magical: bismuth ferrite. Again, she examined a thin film of the material using DFT calculations on “Piz Daint”, this time to determine its potential in catalysis of water splitting — a chemical reaction that splits water molecules into hydrogen and oxygen and can be used for hydrogen production. Current hydrogen production methods are flawed, being either dependent on fossil fuels or else costly and energy demanding. Therefore, developing more efficient technology for water splitting could lead to an eco-friendly hydrogen economy.

As Gattinoni’s calculations showed, bismuth ferrite nano-sheets could indeed be used as a catalyst to boost the reaction. Its electronic properties are surprising, in that the material film remains ferroelectric down to a thinness of a single unit cell — and this without needing any external charge adsorption. This is because bismuth ferrite contains two different types of polarisation: the ferroelectric polarisation and an inbuilt polarisation arising from the material’s bismuth oxide layer being positively charged and the iron oxide layer negatively charged. By coincidence, these two opposed polarisation types possess the same magnitude. Therefore, this inbuilt polarisation exactly compensates the ferroelectric polarisation and adsorbs the surface charges.

A convenient catalyst

This “magical” property makes the material inert, meaning not likely to induce a chemical reaction. If added to water, for instance, nothing will happen. However, if the ferroelectric polarisation is forcibly reversed by applying an electric field, a massive build-up of surface charges occurs, which, in turn, induces the water molecules to split.

Currently, Gattinonis collaborators are working on the experimental confirmation of the idea. In addition, her results as well as previous work from other scientists indicate that an equivalent setup could also be used to degrade pollutants such as toxic nitrogen oxides (NOx). “We will certainly further explore the potential of ferroelectrics for catalysis.”

This text by Santina Russo first appeared in English on the external page CSCS website.