Highly stretchable and self-healing cellulose nanofiber-mediated conductive hydrogel towards strain sensing application.

HYPOTHESIS: Hydrogel-based sensors have attracted considerable attention due to potential opportunities in human health monitoring when both mechanical flexibility and sensing ability are required. Therefore, the integration of excellent mechanical properties, electrical conductivity and self-healing properties into hydrogels may improve the application range and durability of hydrogel-based sensors. EXPERIMENTS: A novel composite hydrogel composed of polyaniline (PANI), polyacrylic acid (PAA) and 2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO)-oxidized cellulose nanofibrils (TOCNFs) was designed. The viscoelastic, mechanical, conductive, self-healing and sensing properties of hydrogels were studied. FINDINGS: The TOCNF/PANI/PAA hydrogel exhibits a fracture strain of 982%, tensile strength of 74.98 kPa and electrical conductivity of 3.95 S m-1, as well as good mechanical and electrical self-healing properties within 6 h at ambient temperature without applying any stimuli. Furthermore, owing to the high sensitivity of the TOCNF/PANI/PAA-0.6 hydrogel-based strain sensor (gauge factor, GF = 8.0), the sensor can accurately and rapidly detect large-scale motion and subtle localized activity. The proposed composite hydrogel is as a promising material for use as soft wearable sensors for health monitoring and smart robotics applications.

A stretchable, self-healing conductive hydrogels based on nanocellulose supported graphene towards wearable monitoring of human motion.

Stretchable, self-healing and conductive hydrogels have attracted much attention for wearable strain sensors, which are highly required in health monitoring, human-machine interaction and robotics. However, the integration of high stretchability, self-healing capacity and enhanced mechanical performance into one single conductive hydrogel is still challenging. In this work, a type of stretchable, self-healing and conductive composite hydrogels are fabricated by uniformly dispersing TEMPO-oxidized cellulose nanofibers (TOCNFs)-graphene (GN) nanocomposites into polyacrylic acid (PAA) hydrogel through an in-situ free radical polymerization. The resulting hydrogels demonstrate a stretchability (∼850 %), viscoelasticity (storage modulus of 32 kPa), mechanical strength (compression strength of 2.54 MPa, tensile strength of 0.32 MPa), electrical conductivity (∼ 2.5 S m-1) and healing efficiency of 96.7 % within 12 h. The hydrogel-based strain sensor shows a high sensitivity with a gauge factor of 5.8, showing great potential in the field of self-healing wearable electronics.

A Skin-Inspired Stretchable, Self-Healing and Electro-Conductive Hydrogel with A Synergistic Triple Network for Wearable Strain Sensors Applied in Human-Motion Detection.

Keywords: nanocellulose; polyacrylic acid; polypyrrole; hydrogel; self-healing and conductive.