Publication

Operando identification of a side-on nickel superoxide intermediate and the mechanism of oxygen evolution on nickel oxyhydroxide

Xile Hu, Lichen Bai, Seunghwa Lee
2023
Journal paper
Abstract

The oxygen evolution reaction (OER) is a key electrochemical reac-tion relevant to energy storage. Ni-containing bimetallic oxyhydrox-ides are among the most active OER catalysts in alkaline medium, but the mechanism of OER on pure Ni oxyhydroxide remains un-clear. Here we combine multiple operando spectroscopic tools including X-ray absorption, ultraviolet visible (UV-Vis), and Raman with electrokinetics to study the mechanism of OER on Ni(OH)2 nanosheets. The spectroscopic data reveal two intermediates. The first one is a Ni(III)-O center dot species formed upon a 2-e oxidation of Ni(OH)2, and the second one is a Ni-OO-Ni species formed upon a 1-e oxidation of Ni(III)-O center dot. The Ni-OO-Ni species is a side-on super-oxide that acts as a site for hole accumulation. The reaction kinetics follows an inner-sphere model. The rate-determining step is OH -attack to Ni(III)-O center dot, chemically driven by the Ni-OO-Ni species. This work provides new experimental fingerprints and mechanistic perspectives for the understanding of Ni-based OER catalysts.

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Related concepts (34)
Oxygen
Oxygen is the chemical element with the symbol O and atomic number 8. It is a member of the chalcogen group in the periodic table, a highly reactive nonmetal, and an oxidizing agent that readily forms oxides with most elements as well as with other compounds. Oxygen is Earth's most abundant element, and after hydrogen and helium, it is the third-most abundant element in the universe. At standard temperature and pressure, two atoms of the element bind to form dioxygen, a colorless and odorless diatomic gas with the formula O2.
Rate equation
In chemistry, the rate law or rate equation for a chemical reaction is a mathematical equation that links the rate of forward reaction with the concentrations or pressures of the reactants and constant parameters (normally rate coefficients and partial reaction orders). For many reactions, the initial rate is given by a power law such as where [\mathrm{A}] and [\mathrm{B}] express the concentration of the species \mathrm{A} and \mathrm{B}, usually in moles per liter (molarity, M).
Rate-determining step
In chemical kinetics, the overall rate of a reaction is often approximately determined by the slowest step, known as the rate-determining step (RDS or RD-step or r/d step) or rate-limiting step. For a given reaction mechanism, the prediction of the corresponding rate equation (for comparison with the experimental rate law) is often simplified by using this approximation of the rate-determining step. In principle, the time evolution of the reactant and product concentrations can be determined from the set of simultaneous rate equations for the individual steps of the mechanism, one for each step.
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