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Zinc-electrode morphology in acid-battery electrolytes

Conference ·
OSTI ID:6606590
This work includes an investigation of zinc deposition from both ZnCl/sub 2/ and ZnBr/sub 2/ electrolytes. The techniques used are cyclic voltammetry, the potential step method and scanning electron microscopy. Apart from the electrolyte the variables investigated were the substrate (zinc, glassy carbon and pyrolytic graphite), fluorinated surfactants, inorganic additives (Pb/sup + +/, Br/sup + + +/) and the superimposition of square wave pulses. Results, which could be fitted to reasonable models, could only be obtained after careful attention was given to electrolyte purity, electrode surface preparation and elimination of the resistance component from the potential measurements. The complexing ion greatly affects the kinetics of zinc deposition. In pure electrolytes the nucleation overvoltage for zinc deposition on glassy carbon was approx. 12mV in 3M ZnBr/sub 2/ and approx. 17mV in 3M ZnCl/sub 2/. The kinetics were much faster in ZnBr/sub 2/ electrolytes. The growth of zinc on glassy carbon could be described by a model that assumes instantaneous nucleation of three dimensional centers and growth under kinetic control. When zinc is deposited on zinc, there is no observable nucleation overvoltage and growth occurs with the simultaneous formation of two dimensional layers and the nucleation and growth of three dimensional centers.
Research Organization:
Brookhaven National Lab., Upton, NY (USA)
DOE Contract Number:
AC02-76CH00016
OSTI ID:
6606590
Report Number(s):
BNL-32190; CONF-821211-3; ON: DE83003959
Country of Publication:
United States
Language:
English