RESUMEN
Zn-air batteries (ZABs) are a promising technology; however, their commercialization is limited by challenges, including those occurring in the electrolyte, and thus, gel polymer electrolytes (GPEs) and hydrogels have emerged as substitutes for traditional aqueous electrolytes. In this work, PVA/PAA membranes were synthesized by the solvent casting method and soaked in 6 M KOH to act as GPEs. The thickness of the membrane was modified (50, 100, and 150 µm), and after determining the best thickness, the membrane was modified with synthesized SiO2 nanospheres and multi-walled carbon nanotubes (CNTs). SEM micrographs revealed that the CNTs displayed lengths of tens of micrometers, having a narrow diameter (95 ± 7 nm). In addition, SEM revealed that the SiO2 nanospheres had homogeneous shapes with sizes of 110 ± 10 nm. Physicochemical experiments revealed that SiO2 incorporation at 5 wt.% increased the water uptake of the PVA/PAA membrane from 465% to 525% and the ionic conductivity to 170 mS cm-1. The further addition of 0.5 wt.% CNTs did not impact the water uptake but it promoted a porous structure, increasing the power density and the stability, showing three-times-higher rechargeability than the ZAB operated with the PVA/PAA GPE.
RESUMEN
In this work, the proof of concept of a functional membraneless microfluidic Zn-air cell (µZAC) that operates with a flow-through arrangement is presented for the first time, where the activity and durability can be modulated by electrodepositing Zn on porous carbon electrodes. For this purpose, Zn electrodes were obtained using chronoamperometry and varying the electrodeposition times (20, 40, and 60 min), resulting in porous electrodes with Zn thicknesses of 3.3 ± 0.3, 11.6 ± 2.4, and 34.8 ± 5.1 µm, respectively. Pt/C was initially used as the cathode to analyze variables, such as KOH concentration and flow rate, and then, two manganese-based materials were evaluated (α-MnO2 and MnMn2O4 spinel, labeled as Mn3O4) to determine the effect of inexpensive materials on the cell performance. According to the transmission electron microscopy (TEM) results, α-MnO2 has a nanorod-like shape with a diameter of 11 ± 1.5 nm, while Mn3O4 presented a hemispherical shape with an average particle size of 22 ± 1.8 nm. The use of α-MnO2 and Mn3O4 cathodic materials resulted in cell voltages of 1.39 and 1.35 V and maximum power densities of 308 and 317 mW cm-2, respectively. The activities of both materials were analyzed through density of state calculations; all manganese species in the α-material MnO2 presented an equivalent density of states with a reduced orbital occupation to the left of the Fermi energy, which allowed for better global performance above Mn3O4/C and Pt/C.