Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1286462 | Journal of Power Sources | 2007 | 9 Pages |
The effect of charge–discharge cycling on the capacity of surface-adhered nickel hydroxide (Ni(OH)2) micro-particles is investigated in aqueous KOH by cyclic voltammetry, and compared with that for pasted nickel hydroxide electrodes. Cyclic voltammetry on adhered Ni(OH)2 micro-particles enables rapid screening of four types of commercially available, battery-grade, nickel hydroxide samples and allows the separation of the oxidation process from the oxygen evolution reaction. With large pasted electrodes, due to their high uncompensated resistance (Ru), these processes are poorly resolved. Pasted β-nickel hydroxide electrodes with a specific capacity of between 190 and 210 mAh g−1 are charged and discharged at constant currents greater than 15 C (18 mA cm−2). With no voltage limit in the charging profile, excess oxygen evolution occurs and capacity fading is observed within the first 50 cycles. Loss of capacity is attributed to the degradation of the electrode due to excess oxygen evolution at switching potentials greater than 0.55 V versus Hg/HgO (1 M KOH). X-ray diffraction (XRD) measurements confirm the formation of γ-NiOOH in these electrodes. Limiting the cell voltage to 1.5 V, and thereby minimizing oxygen evolution, results in no observed capacity loss within 100 cycles, and only β-Ni(OH)2 can be detected by XRD phase analysis.