
Journal of the Electrochemical Society p. 1598 - 1607 (1998)
Update date:2022-08-17
Topics:
Carlin, Richard T.
De Long, Hugh C.
Fuller, Joan
Trulove, Paul C.
Chronoamperometric data collected at a 250 μm tungsten microelectrode were analyzed under near-steady-state conditions to determine the composition of MAlx alloys (M = Co, Ni, Fe, Cu, and Ag) electrodeposited from 1.5:1.0 AlCl3:1-ethyl-3-methylimidazolium chloride room temperature ionic liquids. The analysis method relied on the fact that these alloys are produced by an underpotential deposition mechanism. Results were consistent with previous studies showing that the CoAlx, FeAlx, and CuAlx systems tended to produce alloys with x ≈ 1. Analysis of the NiAlx data was complicated by kinetic phenomena, while data analysis of the AgAlx. system was precluded by dendritic growth of the electrodeposit. All the alloy systems showed complex anodic stripping voltammetric behavior, and the nature of the oxidation processes (e.g., metal anodization, alloy anodization, or selective dealloying) are different for electrodeposits produced in specific potential regimes. Nonlinear curve fitting of the Chronoamperometric data to the appropriate short-time and long-time equations gave diffusion coefficients from 3.9 × 10-7 to 8.3 × 10-7 cm2 s-1 for the transition metal ions in the ionic liquid electrolyte at ca. 22°C.
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