Ionic liquid-enabled hydrogen-bonding networks in corn stalk-derived cellulose/poly(butylene succinate) composite films for sustainable flexible sensors.

Flexible wearable sensors hold great promise for applications in electronic skin, health monitoring, and human-computer interaction. However, conventional sensors often struggle to balance sustainability, mechanical robustness, and sensing accuracy. Herein, we report a sustainable controlled incomplete regeneration strategy to fabricate multifunctional composite films by precisely locking trace ionic liquid ([BMIM]Cl) within a poly(butylene succinate) (PBS)-toughened cellulose matrix. This design achieves a unique performance synergy, the PBS skeleton provides structural reinforcement to counteract IL-induced plasticization, while the residually locked IL establishes continuous ionic pathways and imparts flexibility. The resulting IL/PBS/RC composite films exhibited remarkable performance, including a high tensile strength of 106 MPa, an elongation at break of 21.61%, and stable electrical conductivity. Crucially, this synergistic structure resolves the intrinsic trade-off between strength and conductivity. The assembled sensors demonstrated high linearity (gauge factor, GF = 4.65) and optical transparency, enabling visualizable, real-time monitoring of respiratory patterns and joint movements. This work establishes a scalable, eco-friendly material platform for high-performance wearable electronics, valorizing agricultural waste into functional smart devices.