Self-healing materials have been attracting the attention of the scientists over the past few decades because of their effectiveness in detecting damage and their autonomic healing response. Self-healing materials are an evolving and intriguing field of study that could lead to a substantial increase in the lifespan of materials, improve the reliability of materials, increase product safety, and lower product replacement costs. Within the past few years, various autonomic and non-autonomic self-healing systems have been developed using various approaches for a variety of applications. The inclusion of appropriate functionalities into these materials by various chemistries has enhanced their repair mechanisms activated by crack formation. This review article summarizes various self-healing techniques that are currently being explored and the associated chemistries that are involved in the preparation of self-healing composite materials. This paper further surveys the electronic applications of self-healing materials in the fields of energy harvesting devices, energy storage devices, and sensors. We expect this article to provide the reader with a far deeper understanding of self-healing materials and their healing mechanisms in various electronics applications.

Background: Dye contamination of natural water system is a severe problem due to the considerable enhancement in industrial activities. As the dyes are highly visible, non-biodegradable, and toxic in nature, they are considered as a severe source of water pollution. Therefore, it is imperative to develop an inexpensive, simple, effective, and easy technique for their elimination from wastewater. Methods: Luffa aegyptiaca peel (LuAP), kitchen waste was exploited as a low-priced biosorbent for the adsorptive elimination of cationic methylene blue (MB) dye. The influence of several batch parameters, i.e., adsorbent dose, pH of the solution, different initial dye concentration, adsorbate/adsorbent contact time, and temperature were optimized for maximum adsorption of MB from aqueous media. Furthermore, thermodynamics, kinetics, and isotherm studies were also carried out in order to comprehend the dominant mechanism for the adsorptive elimination of MB. Results: The kinetic data for the adsorption of MB onto the LuAP followed closely by the pseudo-second-order (PSO) equation, and the adsorption equilibrium data were observed to be well demonstrated by Langmuir isotherm. The equilibrium was attained in 180 min with maximum sorption capacity of 52.63 mg/g at an adsorbent dose 3 g/L, pH of 7, and temperature 303 K. Thermodynamic study reveals that the removal of MB by LuAP is spontaneous and endothermic. Conclusion: It has been concluded that LuAP can be efficiently utilized for the confiscation of cationic MB dye from polluted water.