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      Comparative Electrocatalytic Oxygen Evolution Reaction Studies of Spinel NiFe2O4 and Its Nanocarbon Hybrids

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          Abstract

          Electrocatalytic oxygen evolution reaction (OER) is one of the crucial reactions for converting renewable electricity into chemical fuel in the form of hydrogen. To date, there is still a challenge in designing ideal cost-effective OER catalysts with excellent activity and robust durability. The hybridization of transition metal oxides and carbonaceous materials is one of the most effective and promising strategies to develop high-performance electrocatalysts. Herein, this work synthesized hybrids of NiFe 2O 4 spinel materials with two-dimensional (2D) graphene oxide and one-dimensional (1D) carbon nanotubes using a facile solvothermal approach. Electrocatalytic activities of NiFe 2O 4 with 2D graphene oxide toward OER were realized to be superior even to the 1D carbon nanotube-based electrocatalyst in terms of overpotential to reach a current density of 10 mA/cm 2 as well as Tafel slopes. The NiFe 2O 4 with 2D graphene oxide hybrid exhibits good stability with an overpotential of 327 mV at a current density of 10 mA/cm 2 and a Tafel slope of 103 mV/dec. The high performance of NiFe 2O 4 with 2D graphene oxide is mainly attributed to its unique morphology, more exposed active sites, and a porous structure with a high surface area. Thus, an approach of hybridizing a metal oxide with a carbonaceous material offers an attractive platform for developing an efficient electrocatalyst for water electrochemistry applications.

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          Most cited references49

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          Solar water splitting cells.

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            Universality in Oxygen Evolution Electrocatalysis on Oxide Surfaces

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              Mechanistic studies of the oxygen evolution reaction by a cobalt-phosphate catalyst at neutral pH.

              The mechanism of the oxygen evolution reaction (OER) by catalysts prepared by electrodepositions from Co(2+) solutions in phosphate electrolytes (Co-Pi) was studied at neutral pH by electrokinetic and (18)O isotope experiments. Low-potential electrodepositions enabled the controlled preparation of ultrathin Co-Pi catalyst films (<100 nm) that could be studied kinetically in the absence of mass transport and charge transport limitations to the OER. The Co-Pi catalysts exhibit a Tafel slope approximately equal to 2.3 × RT/F for the production of oxygen from water in neutral solutions. The electrochemical rate law exhibits an inverse first order dependence on proton activity and a zeroth order dependence on phosphate for [Pi] ≥ 0.03 M. In the absence of phosphate buffer, the Tafel slope is increased ∼3-fold and the overall activity is greatly diminished. Together, these electrokinetic studies suggest a mechanism involving a rapid, one electron, one proton equilibrium between Co(III)-OH and Co(IV)-O in which a phosphate species is the proton acceptor, followed by a chemical turnover-limiting process involving oxygen-oxygen bond coupling.
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                Author and article information

                Journal
                Transactions of Tianjin University
                Trans. Tianjin Univ.
                Springer Science and Business Media LLC
                1006-4982
                1995-8196
                February 2022
                December 10 2021
                February 2022
                : 28
                : 1
                : 80-88
                Article
                10.1007/s12209-021-00310-x
                4c828adf-7b0d-4518-913e-2c7dec4ea458
                © 2022

                https://creativecommons.org/licenses/by/4.0

                https://creativecommons.org/licenses/by/4.0

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