Abstract

Zinc-air batteries are a promising technology for large-scale electricity storage. However, their practical deployment has been hindered by some issues related to corrosion and passivation of the zinc anode in an alkaline electrolyte. In this work, anionic surfactant sodium dodecyl sulfate (SDS) and nonionic surfactant Pluronic F-127 (P127) are examined their applicability to enhance the battery performances. Pristine zinc granules in 7 M KOH, pristine zinc granules in 0–8 mM SDS/7 M KOH, pristine zinc granules in 0–1000 ppm P127/7 M KOH, and SDS coated zinc granules in 7 M KOH were examined. Cyclic voltammograms, potentiodynamic polarization, and electrochemical impedance spectroscopy confirmed that using 0.2 mM SDS or 100 ppm P127 effectively suppressed the anode corrosion and passivation. Nevertheless, direct coating SDS on the zinc anode showed adverse effects because the thick layer of SDS coating acted as a passivating film and blocked the removal of the anode oxidation product from the zinc surface. Furthermore, the performances of the zinc-air flow batteries were studied. Galvanostatic discharge results indicated that the improvement of discharge capacity and energy density could be sought by the introduction of the surfactants to the KOH electrolyte. The enhancement of specific discharge capacity for 30% and 24% was observed in the electrolyte containing 100 ppm P127 and 0.2 mM SDS, respectively.

Highlights

  • Electrolyte plays an essential role in battery electrochemistry affecting the transport properties of the active species between the anode and the cathode

  • The primary objective of this work is to examine the effects of sodium dodecyl sulfate (SDS), which is an anionic surfactant, and Pluronic F-127 (P127), which is a nonionic surfactant, on the electrochemical behavior of zinc granules used in zinc-air flow batteries

  • cyclic voltammetry (CV) measurements were recorded in the voltage ranging from −1.8 to 0.8 V vs. Hg/HgO using a potential scan rate of 0.05 V/s unless otherwise specified

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Summary

Introduction

Electrolyte plays an essential role in battery electrochemistry affecting the transport properties of the active species between the anode and the cathode. The passivation effect is known as the result of zinc oxide (ZnO) deposition on the active zinc surface. Aluminum oxide (Al2O3) as a surface modification exhibited the positive effect on controlling the hydrogen evolution reaction (HER) for zinc-air batteries[20]. Corrosion and passivation behaviors of planar zinc was studied in electrolytes containing KOH, ZnO and a cationic surfactant dodecyltrimethylammonium bromide (DTAB)[24]. Ghavami et al.[29] studied the effects of cationic surfactant cetyl trimethylammonium bromide (CTAB) and SDBS on the performance of Zn–MnO2 alkaline batteries. The negative charge polar group of SDBS coordinated to zinc ions at the anode surface leading to a generation of small zinc oxide particles. The positive charge polar group of CTAB showed weak interaction with the zinc ions leading to a generation of larger zinc oxide particles. The results revealed that SDS outperformed CTAB, and significantly enhanced the cycle life of the batteries

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