The development of soft electronic devices capable of autonomous self-healing (SH) holds immense potential across various endeavours, promising to revolutionize product durability, reliability, and maintenance practices. Despite some progress has been made, underwater stable SH continues to be an active area of research. Herein, SH polymer PDMS-MDI0.4-TFB0.6 (SHP) with excellent mechanical property was composited with MXene to investigate the piezoelectric nature under various circumstance. By leveraging MXene into SHP not only improves the material properties of mechanical stress but also permittivity of the elastomer. Thus, MXene incorporated SHP (mSHP) induce high polarized charges under mechanical pressure. The fabrication of mSHP piezoelectric nanogenerator (mSHP-PENG) device via spray coating AgNWs on the surface forms ohmic contact, which facilitate high sensitivity and flexibility. Nevertheless, the generated piezoelectricity (30 V, 4.2 μA: 3 Hz) upon mechanical pressure gives maximum power density of 128 μW/m2 indicating that our device can act as a reliable power source for portable electronic gadgets. In addition, SHP with amphiphilic functional groups sustain the original shape even after immerse into water for so long. Taking this into account, our device undergoes effective deformation even at low pressures, thus render to fabricate touch sensitive piezo-switches for both atmospheric and aquatics environments.

Self-healing soft electronic material composition is crucial to sustain the device long-term durability. The fabrication of self-healing soft electronics exposed to high moisture environment is a significant challenge that has yet to be fully achieved. This paper presents the novel concept of a water-assisted room-temperature autonomous self-healing mechanism based on synergistically dynamic covalent Schiff-based imine bonds with hydrogen bonds. The supramolecular water-assisted self-healing polymer (WASHP) films possess rapid self-healing kinetic behavior and high stretchability due to a reversible dissociation–association process. In comparison with the pristine room-temperature self-healing polymer, the WASHP demonstrates favorable mechanical performance at room temperature and a short self-healing time of 1 h; furthermore, it achieves a tensile strain of 9050%, self-healing efficiency of 95%, and toughness of 144.2 MJ m⁻³. As a proof of concept, a versatile WASHP-based light-emitting touch-responsive device (WASHP-LETD) and perovskite quantum dot (PeQD)-based white LED backlight are designed. The WASHP-LETD has favorable mechanical deformation performance under pressure, bending, and strain, whereas the WASHP-PeQDs exhibit outstanding long-term stability even over a period exceeding one year in a boiling water environment. This paper provides a mechanically robust approach for producing eco-friendly, economical, and waterproof e-skin device components.