Poly(glycerol sebacate)-based soft-tissue-mimicked active layers for triboelectric nanogenerators

Abstract

Herein poly(glycerol sebacate) (PGS) has been synthesized and characterized to identify it’s potential as an active triboelectric layer in implantable and biodegradable TENG devices. The implantable and biodegradable TENG devices require excellent triboelectric properties, as well as the ability to mimic the mechanical properties of the surrounding tissues and exhibiting low cytotoxicity and eventual degradation and removal by bio-absorption. Two-step synthesis of PGS was carried out by using polycondensation between glycerol and sebacic acid in 1:1 molar ratio, followed by film preparation by spray-coating of the prepolymer solution. Crosslinking conditions were elaborated to yield good triboelectric performance together with low cytotoxicity. Triboelectric surface charge density of up to 0.188 nC cm−2 was obtained, exceeding the values of common triboelectric materials such as PDMS and PTFE by 2.89 and 3.76 times, respectively, when tested under identical contact-separation parameters. The mechanical properties of PGS can be tuned by varying the crosslinking degree to mimic soft tissues. In this context, in vitro studies on human skin fibroblasts revealed cell viability up to 78%. Furthermore, the cell viability is found to be strongly related to the crosslinking time of the PGS. The results show significantly lower cytotoxicity as compared to, for example, poly(sorbitol sebacate) and poly(hexanediol-co-citric acid). The flexibility and the confirmed biocompatibility beside the unique mechanical and physio-chemical collective properties of the of the polymer demonstrates the potential use of PGS for the next generation of implantable TENG devices. Graphical abstract