Control engineering

Nanotechnology

Electrode

Organic chemistry

Electrical conductor

Decoupling (probability)

Crystallography

Biology

Crystal structure

Endocrinology

Ionic conductivity

Engineering

Conductivity

Physical chemistry

Chemical physics

Composite material

Ionic bonding

Chemistry

Materials science

Lithium (medication)

Electrolyte

Supramolecular chemistry

Nature Communications

The emergence of wearable electronics puts batteries closer to the human skin, exacerbating the need for battery materials that are robust, highly ionically conductive, and stretchable. Herein, we introduce a supramolecular design as an effective strategy to overcome the canonical tradeoff between mechanical robustness and ionic conductivity in polymer electrolytes. The supramolecular lithium ion conductor utilizes orthogonally functional H-bonding domains and ion-conducting domains to create a polymer electrolyte with unprecedented toughness (29.3 MJ m-3) and high ionic conductivity (1.2 × 10-4 S cm-1 at 25 °C). Implementation of the supramolecular ion conductor as a binder material allows for the creation of stretchable lithium-ion battery electrodes with strain capability of over 900% via a conventional slurry process. The supramolecular nature of these battery components enables intimate bonding at the electrode-electrolyte interface. Combination of these stretchable components leads to a stretchable battery with a capacity of 1.1 mAh cm-2 that functions even when stretched to 70% strain. The method reported here of decoupling ionic conductivity from mechanical properties opens a promising route to create high-toughness ion transport materials for energy storage applications.

Decoupling of mechanical properties and ionic conductivity in supramolecular lithium ion conductors