Reversible and irreversible transformations of Ni-based electrocatalysts during the oxygen evolution reaction AITranslate
Abstract AITranslate
Highlights • Significant, OER-driven changes in Ni-based materials preclude their active state. • This includes phase transformations of NiO, Ni(OH)2, and NiOOH caused by applied potential, pH changes and ageing. • Under OER conditions, Ni and Fe can experience reversible oxidation to the +IV state. • Lattice oxygen participation in the reaction mechanism can increase OER activity. • The uptake of electrolyte Fe impurities can influence the Ni electronic/geometric structure. Nickel-based catalysts for the alkaline oxygen evolution reaction (OER) demonstrate excellent catalytic performance and stability. However, a lack of fundamental understanding of the dynamic electronic and structural changes that occur under OER conditions inhibits the rational design of new materials. Recent advances in operando spectroscopy and computational modeling techniques have helped to elucidate the electrochemically-driven transformations of Ni-based materials. For reversible transformations, this encompasses an increased understanding of the redox transformations of Ni/Fe centers, the adsorption and desorption of reaction intermediates, oxygen vacancy dynamics, phase transformations, and the mechanism of dissolution and redeposition of surface atoms. Likewise, there have been great advances in scientific understanding of irreversible transformations including phase transformations related to ageing, as well as operando surface reconstruction which involves the growth of new OER active phases. Graphical abstract Download : Download high-res image (230KB) Download : Download full-size image
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DOI:https://doi.org/10.1016/j.coelec.2023.101231
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Highlights • Significant, OER-driven changes in Ni-based materials preclude their active state. • This includes phase transformations of NiO, Ni(OH)2, and NiOOH caused by applied potential, pH changes and ageing. • Under OER conditions, Ni and Fe can experience reversible oxidation to the +IV state. • Lattice oxygen participation in the reaction mechanism can increase OER activity. • The uptake of electrolyte Fe impurities can influence the Ni electronic/geometric structure. Nickel-based catalysts for the alkaline oxygen evolution reaction (OER) demonstrate excellent catalytic performance and stability. However, a lack of fundamental understanding of the dynamic electronic and structural changes that occur under OER conditions inhibits the rational design of new materials. Recent advances in operando spectroscopy and computational modeling techniques have helped to elucidate the electrochemically-driven transformations of Ni-based materials. For reversible transformations, this encompasses an increased understanding of the redox transformations of Ni/Fe centers, the adsorption and desorption of reaction intermediates, oxygen vacancy dynamics, phase transformations, and the mechanism of dissolution and redeposition of surface atoms. Likewise, there have been great advances in scientific understanding of irreversible transformations including phase transformations related to ageing, as well as operando surface reconstruction which involves the growth of new OER active phases. Graphical abstract Download : Download high-res image (230KB) Download : Download full-size image
quote
| GB/T 7714-2015 | [1] Natasha Hales, Thomas Justus Schmidt, Emiliana Fabbri. Current Opinion in Electrochemistry, 2023(38). DOI:10.1016/j.coelec.2023.101231. |
| MLA | [1] Natasha Hales, et al., Current Opinion in Electrochemistry, no. 38, 2023, https://doi.org/10.1016/j.coelec.2023.101231. |
| APA | [1] Natasha Hales, Thomas Justus Schmidt, & Emiliana Fabbri. (2023). Current Opinion in Electrochemistry(38). https://doi.org/10.1016/j.coelec.2023.101231 |
| IEEE | [1] Natasha Hales, Thomas Justus Schmidt, and Emiliana Fabbri, Current Opinion in Electrochemistry, no. 38, 2023, doi: 10.1016/j.coelec.2023.101231. keywords: {Water splitting;Electrolysis;Nickel;Oxide;Hydroxide;Oxyhydroxide;OER;Operando} |
