This study presents a novel non-aqueous Al–air battery utilizing 1-ethyl-3-methylimidazolium oligo-fluoro-hydrogenate room temperature ionic liquid. The Al–air-RTIL system can sustain current densities up to 1.5 mA cm−2, producing capacities above 140 mA h cm−2, thus utilizing above 70% of the theoretical Al capacity.

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Silicon electrochemistry in fluorohydrogenate ionic liquids is partly hampered owing to the incapability of producing an accurate and reproducible potential measurement due to a lack of appropriate reference electrodes. This research work describes a simple assembly of a stable external reference electrode enabling accurate studies of silicon electrochemistry in fluorohydrogenate ionic liquids. The electrode configuration is based on the ferrocene/ferrocenium (Fc|Fc(+)) couple dissolved in the EMIm(HF)(2.3)F (1-ethyl-3-methyl-imidazolium fluorohydrogenate)/Carbopol 941 gel. A stable potential of 2.5 wt% Carbopol-based electrode was measured versus a calomel reference electrode at 250 ± 3 mV. By utilizing the constructed electrode, an intensive electrochemical investigation on n-type silicon in EMIm(HF)(2.3)F was conducted. Flat-band and open circuit potentials were measured, along with Si-air half- and full-cell electrochemical measurements. A suggested mechanism for the n-type Si dissolution process in the EMIm(HF)(2.3)F electrolyte, without illumination, is discussed as well.

Aluminum (Al) electrochemical dissolution in organic nonaqueous media and room temperature ionic liquids (RTILs) is partially hampered by the presence of a native oxide. In this work, Al activation in EMIm(HF)2.3F RTIL is reported. It was confirmed that as a result of the interaction of Al with the RTIL, a new film is formed instead of the pristine oxide layer. Aluminum surface modifications result in a transformation from a passive state to the active behavior of the metal. This was confirmed via the employment of electrochemical methods and characterization by XPS, AFM, and TEM. It was shown that the pristine oxide surface film dissolves in EMIm(HF)2.3F, allowing an Al-O-F layer to be formed instead. This newly built up layer dramatically restricts Al corrosion while enabling high rates of Al anodic dissolution. These beneficial features allow the implementation of Al as an anode in advanced portable power sources, such as aluminum-air batteries.