Self-Healing Smartphones on the Horizon

The key to self-repair is in the chemical bonding. Two types of bonds exist in materials, Wang explains. There are covalent bonds, which are strong and don’t readily reform once broken; and noncovalent bonds, which are weaker and more dynamic. For example, the hydrogen bonds that connect water molecules to one another are non-covalent, breaking and reforming constantly to give rise to the fluid properties of water. “Most self-healing polymers form hydrogen bonds or metal-ligand coordination, but these aren’t suitable for ionic conductors,” Wang says.

Wang’s team at the University of California, Riverside, turned instead to a different type of non-covalent bond called an ion-dipole interaction, a force between charged ions and polar molecules. “Ion-dipole interactions have never been used for designing a self-healing polymer, but it turns out that they’re particularly suitable for ionic conductors,” Wang says. The key design idea in the development of the material was to use a polar, stretchable polymer, poly(vinylidene fluoride-co-hexafluoropropylene), plus a mobile, ionic salt. The polymer chains are linked to each other by ion-dipole interactions between the polar groups in the polymer and the ionic salt.

 

Credit: The American Chemical Society

The resulting material could stretch up to 50 times its usual size. After being torn in two, the material automatically stitched itself back together completely within one day.

As a test, the researchers generated an “artificial muscle” by placing a non-conductive membrane between two layers of the ionic conductor. The new material responded to electrical signals, bringing motion to these artificial muscles, so named because biological muscles similarly move in response to electrical signals (though Wang’s materials are not intended for medical applications).

For the next step, the researchers are working on altering the polymer to improve the material’s properties. For example, they are testing the material in harsh conditions, such as high humidity. “Previous self-healing polymers haven’t worked well in high humidity, Wang says. “Water gets in there and messes things up. It can change the mechanical properties. We are currently tweaking the covalent bonds within the polymer itself to get these materials ready for real-world applications.”

Wang acknowledges funding from start-up funds from the University of California, Riverside.

The researchers presented their work today at the 253rd National Meeting & Exposition of the American Chemical Society (ACS). ACS, the world’s largest scientific society, is holding the meeting in San Francisco through Thursday. It features more than 14,000 presentations on a wide range of science topics.