Polymer electrolytes have been explored as an alternative to conventional aqueous electrolytes in zinc-ion batteries, particularly for flexible and wearable applications. Despite the increasing interest in polymer electrolyte-based zinc-ion batteries (ZIBs), their development is still in its early stages due to various challenges. In this study, we investigated three promising polymer electrolytes: CSAM (carboxyl methyl chitosan with acrylamide monomer), PAM (polyacrylamide monomer hydrogel electrolyte), and p-PBI (phosphate-doped polybenzimidazole solid electrolyte) with Zn(ClO4)2 and Zn(OTf)2, as electrolytes for zinc-ion batteries. The p-PBI solid electrolyte showed high mechanical stability and improved resistance to short-circuiting during cycling. The presence of carboxyl groups in CSAM and the existence of O-H bonding facilitated ion movement, resulting in enhanced ionic conductivity and preventing dendrite formation. Incorporating these hydrogels with high-performance zinc salts, such as zinc triflate (Zn(OTf)2), resulted in stable symmetric cell cycling over 4000 h with a uniform voltage profile under 1 mA/cm2 and a low overpotential of around 53 mV cycling with CSAM. Rate-dependent full-cell testing showed that the PBI solid electrolyte delivers higher capacity retention at different current densities, whereas CSAM exhibits markedly better long-term stability, even at low voltages, owing to its effective dendrite suppression, which helps preserve cathode performance over extended cycling.
Rajabi et al. (2026) studied this question.