In situ STM studies of zinc in aqueous solutions containing PEG DiAcid inhibitor: Correlation with electrochemical performances of zinc-air fuel cells

摘要

Electrochemical performance of prismatic zinc-air fuel cells comprising zinc anode gel containing poly(ethylene glycol) (PEG 600) and poly(ethylene glycol) bis(carboxymethyl) ether (PEG DiAcid 600) as corrosion inhibitor were studied. It was found that in addition to the low zinc corrosion rates obtained from cells utilizing PEG DiAcid 600 as corrosion inhibitor, both analog and global mobile system (GSM) discharge capacities and potential plateaus, in a wide range of temperatures were higher once PEG DiAcid was added to the zinc gel mixtures. The results obtained from in situ scanning tunneling microscopy (STM) studies of zinc substrates immersed in deionized (DI) water containing inhibitors reveal that the film produced on the zinc metal in the presence of PEG DiAcid is by far thinner than the film produced by other inhibitors such as PEG 600 and polyoxyethylene alkyl phosphate ester acid (GAFAC RA 600). These studies also reveal that the addition of PEG DiAcid forms an adherent and a complete protective coverage, while the addition of PEG 600 and GAFAC RA 600 resulted in an incomplete coverage with the appearance of pits and terraces, indicating on a restricted inhibition performance of these two polymers compared with PEG DiAcid. These studies suggest a low interface resistivity of zinc immersed in alkaline solution containing PEG DiAcid, which is expressed in a higher working potential and increased cell capacity in different temperatures at two discharge modes of analog and GSM.