The role of side-chain branching in flexoelectric properties of a flexible, ionic solid polymer electrolyte membrane (PEM) has been investigated subjected to mechanical bending. These PEMs were synthesized via photopolymerization of the bifunctional poly(ethylene glycol) diacrylate (PEGDA) network attached with monofunctional poly(ethylene glycol) methyl ether acrylate (PEGMEA) branches in their ternary mixtures with lithium bis(tri-fluoromethane sulfonyl) imide (LiTFSI) salt. Both the PEGDA polymer precursor and PEGDMA side branches are capable of ionizing the lithium salt, but the dissociated lithium cations can also form the complexation with ether oxygen of PEGDA. With increasing PEGMEA content, not only the glass transition temperature is lowered, but also the ionic conductivity increases with temperature, which may be attributed to plasticization by dangling PEGMEA side chains. The flexoelectric responses of PEMs were investigated under various intermittent and oscillatory cantilever bending modes as a function of PEM composition and frequency. Last but not the least, the mechanoelectrical energy conversion was evaluated for various PEGDA/PEGMEA compositions and discussed its potential applications in energy harvesting from natural resources such as wind and wave motions.
Keywords: Branched network; Energy harvesting; Flexoelectricity; Mechanical deformation; Mechanoelectrical transduction; Polymer electrolyte membranes.