1980
DOI: 10.1016/0013-4686(80)87102-7
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Mechanism of oxygen evolution in basic medium at a nickel electrode

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1980
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Cited by 68 publications
(34 citation statements)
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“…It is our opinion that a systematic and consistent study of the OER at the oxidised surfaces of electrodes of adjacent first row transition metals should prove useful in elucidating whether a common reaction mechanism prevails, and if so, which (if any) of the previously proposed pathways is most likely. Polycrystalline nickel anodes have been commercially utilised in water electrolysis and consequently there exists a significant body of work on this system [24][25][26][27][28][29][30][31][32]. In contrast, we are aware of only three separate studies [33][34][35][36] on the OER at oxidised cobalt electrodes, while our own work [37,38] is, to the best of our knowledge, the only published account of the reaction at oxidised iron anodes.…”
Section: Introductionmentioning
confidence: 81%
“…It is our opinion that a systematic and consistent study of the OER at the oxidised surfaces of electrodes of adjacent first row transition metals should prove useful in elucidating whether a common reaction mechanism prevails, and if so, which (if any) of the previously proposed pathways is most likely. Polycrystalline nickel anodes have been commercially utilised in water electrolysis and consequently there exists a significant body of work on this system [24][25][26][27][28][29][30][31][32]. In contrast, we are aware of only three separate studies [33][34][35][36] on the OER at oxidised cobalt electrodes, while our own work [37,38] is, to the best of our knowledge, the only published account of the reaction at oxidised iron anodes.…”
Section: Introductionmentioning
confidence: 81%
“…[56][57][58][59][60][61][62][63][64] In addition, β-Ni(OH) 2 and β-NiOOH were regarded as superior catalysts compared with α-Ni(OH) 2 and γ-NiOOH because the catalytic efficiency was enhanced upon its transformation from α-Ni(OH) 2 into β-Ni(OH) 2 after electrochemical aging treatment in KOH electrolyte. [54,55] However, Corrigan claimed that the improvement of the catalytic activity after the treatment was not due to phase transformation but due to the incorporation of Fe impurities.…”
Section: Ni-fe Layered Hydroxidementioning
confidence: 99%
“…This high charging voltage may be due to the poor catalytic activity of the platinum/platinum black electrode for the OER at room temperature in the aqueous solution of saturated LiOH with 10 M LiCl. Metal electrodes such as Ag and Ni, which exhibit excellent catalytic activity for the OER in alkaline solution [70,71], were unstable in the (15-30 μm), and the catalytic activities of these electrodes were compared using linear sweep voltammetry [68]. The highest catalytic activity for the OER was observed for RuO 2 in an aqueous solution of saturated LiOH with 10 M LiCl.…”
Section: Cell Performance Of Aqueous Lithium-air Cellsmentioning
confidence: 99%