A nonstoichiometric structural model to characterize changes in the nickel hydroxide electrode during cycling
Experimental capacities and mass changes are v recorded using an electrochemical quartz crystal microbalance during the first nine charge and discharge cycles of nickel hydroxide thin films cycled in 3.0 weight percent (wt%) potassium hydroxide electrolyte. For the first time, the film capacities have been corrected for the oxygen evolution side reaction, and the data used as input into a point defect-containing structural model to track the changes that occur during short-term cycling. Variations in capacity and mass during formation and charge/discharge cycling are related to changes in the point defect parameters, thus providing a structural origin for the unique experimental variations observed here and often reported in the literature, but previously unexplained. Proton-, potassium-, and water-content vary in the active material during charge/discharge cycling. The observed capacity loss, or "capacity fade," is explained by incomplete incorporation of potassium ions in (or near) the nickel vacancy during charge, as additional protons are then allowed to occupy the vacant lattice site. The increase in water content during reduction parallels the expansion of the electrode that is well known during cycling. This result confirms the origin of the swelling phenomenon as being caused by water incorporation. The model and methodology developed in this paper can be used to correlate electrochemical signatures with material chemical structure.
Journal of Solid State Electrochemistry
A nonstoichiometric structural model to characterize changes in the nickel hydroxide electrode during cycling.
Journal of Solid State Electrochemistry,
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/4784