Rechargeable zinc-air batteries (RZABs) with high energy densities and low costs have attracted tremendous interest for meeting the ever-growing demand for flexible and portable applications. In these batteries, the quasisolid/solid-state electrolyte plays a critical role in the battery performance, such as the cycling performance rate and power output. In this study, porous poly (vinyl alcohol) (PVA) and poly (acrylic acid) (PAA) composite gel polymer electrolytes (GPEs) were modified by incorporating SiO2 as a water retainer. For this reason, SiO2 spheres of different sizes were synthesized by varying the temperature (5, 20, 60, and 80 degrees C) and reaction time (2, 6, 18, and 24 h). According to the SEM micrographs, the average size ranged from 107 to 710 nm depending on the conditions. The porous PVA/PAA-SiO2 GPEs obtained by selecting three SiO2 sizes (107, 425, and 630 nm) exhibited higher water retention capability than the unmodified GPE. Among them, the GPE with SiO2-630 nm displayed the highest battery performance (1.46 V, 85 mWcm-2 @ 0.8 V). This was achieved using CoMn2O4 spinel as a bifunctional electrocatalyst, with a catalyst loading of 2 mg cm- 2 . The quasi-solid-state RZAB displayed twice the rechargeability of the RZAB assembled with Pt/C+IrO2/C (120 vs. 62 cycles). According to postmortem tests, this can be related to the improved water retention, the decrease in the size of the formed Zn dendrites, and the stability of the bifunctional material. Thus, fine-tuning of the electrocatalyst/electrolyte interface strongly affects the rechargeability.
