Vanadium Complexes in a Lewis Basic Room-Temperature 1-Ethyl-3-methyl-1H-imidazolium Chloride/Aluminum Chloride Molten Salt

1997 ◽  
Vol 36 (18) ◽  
pp. 4024-4028 ◽  
Author(s):  
Kevin R. Hanz ◽  
Thomas L. Riechel
Keyword(s):  
Molten Salt ◽  
Aluminum Chloride ◽  
Room Temperature ◽  
Vanadium Complexes ◽  
Imidazolium Chloride

Room Temperature Molten Salt Electrolytes for Photoelectrochemical Applications

1982 ◽  
Vol 104 (3) ◽  
pp. 146-152 ◽  
Author(s):  
K. Rajeshwar ◽  
P. Singh ◽  
J. DuBow
Keyword(s):  
Molten Salt ◽  
Room Temperature ◽  
Stability Limit ◽  
Redox System ◽  
Conduction Band Edge ◽  
Cyclic Voltammograms ◽  
Imidazolium Chloride ◽  
Molar Ratios ◽  
The Difference ◽  
Redox Level

Mixtures of aluminum chloride (AlCl3) with triethylammonium chloride (Et3NHCl), 1,6-ethyl lutidinium bromide (EtluBr), tert-butyl pyridinium bromide (BPBr), and dialkyl imidazolium chloride (R2ImCl), in certain molar ratios yielded ionic liquids at room temperature which were studied with respect to their applicability as electrolytes in photoelectrochemical (PEC) cells. Background voltammograms were obtained for these electrolytes on carbon and n-GaAs electrodes. The anodic stability limit was found to be enhanced on n-GaAs relative to carbon in all cases. The cathodic decomposition potential of the electrolyte showed a smaller positive shift on n-GaAs with the exception of the 3:1 AlCl3-BPBr electrolyte. The difference in electrolyte stability behavior on carbon and n-GaAs is interpreted in terms of carrier density effects. Cyclic voltammograms were compared on carbon in the various electrolytes for a model redox system comprising the ferrocene/ferricenium couple. The separation of the cathodic and anodic waves in all the cases was consistent with a quasi-reversible redox behavior—the most sluggish electron transfer being observed in the case of the 3:1 AlCl3-BpBr electrolyte. These results are compared with those obtained previously on the AlCl3-butyl pyridinium chloride (BPC) system. Capacitance-voltage measurements were made on n-GaAs electrodes in contact with the various electrolytes. Flatband-potentials (Vfb) were deduced from these data using Mott-Schottky plots. The relative positions of the n-GaAs band-edges and the redox levels were mapped on a common potential scale utilizing these data. The ferrocene/ferricenium redox level was placed negative of the conduction band-edge in n-GaAs in all the cases. The implications of this result for PEC applications and the role of specific ion adsorption of electrolyte species on the electrostatic aspects of the n-GaAs/molten salt electrolyte interface are discussed with the aid of energy band diagrams.

Electrodeposition of Aluminum from the Aluminum Chloride‐1‐Methyl‐3‐ethylimidazolium Chloride Room Temperature Molten Salt + Benzene

1997 ◽  
Vol 144 (3) ◽  
pp. 936-943 ◽  
Author(s):  
Qing Liao ◽  
William R. Pitner ◽  
Gemma Stewart ◽  
Charles L. Hussey ◽  
Gery R. Stafford
Keyword(s):  
Molten Salt ◽  
Aluminum Chloride ◽  
Room Temperature ◽  
Ethylimidazolium Chloride
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