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X-ray Photoelectron Spectroscopic Investigation of Plasma-Enhanced Chemical Vapor Deposited NiO<sub><i>x</i></sub>, NiO<sub><i>x</i></sub>(OH)<sub><i>y</i></sub>, and CoNiO<sub><i>x</i></sub>(OH)<sub><i>y</i></sub>: Influence of the Chemical Composition on the Catalytic Activity for the Oxygen Evolution Reaction
284
Citations
26
References
2017
Year
Materials ScienceWhereas NioxChemical EngineeringPure NioxEngineeringOxygen Reduction ReactionPhotochemistryInorganic PhotochemistrySurface ElectrochemistryChemical CompositionReactive GasCatalysisCatalytic ActivityHydrogenChemistryElectrode Reaction MechanismOxygen Evolution ReactionElectrochemistry
We report here the plasma-enhanced chemical vapor deposition and electrocatalytic characterization of pure NiOx and NiOx(OH)y. Whereas NiOx is deposited if oxygen is used as a reactive gas, the use of air as a reactive gas leads to the deposition of the NiOx(OH)y, which is electrochemically more active than the NiOx. By recording X-ray photoelectron spectra from the as-deposited catalysts and after their electrochemical investigations, we determined that the electrochemical activity correlates with the amount of hydroxide sites on the surface. Such a behavior was already observed for CoOx and CoOx(OH)y. As a consequence, CoNiOx(OH)y was deposited using air as a reactive gas to study the influence of nickel on the electronic structure of CoOx(OH)y and its effect on the electrochemical activity.
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