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Solvent‐Mediated Control of the Electrochemical Discharge Products of Non‐Aqueous Sodium–Oxygen Electrochemistry

The reduction of dioxygen in the presence of sodium cations can be tuned to give either sodium superoxide or sodium peroxide discharge products at the electrode surface. Control of the mechanistic direction of these processes may enhance the ability to tailor the energy density of sodium–oxygen batt...

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Detalles Bibliográficos
Autores principales: Aldous, Iain M., Hardwick, Laurence J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999043/
https://www.ncbi.nlm.nih.gov/pubmed/27240015
http://dx.doi.org/10.1002/anie.201601615
Descripción
Sumario:The reduction of dioxygen in the presence of sodium cations can be tuned to give either sodium superoxide or sodium peroxide discharge products at the electrode surface. Control of the mechanistic direction of these processes may enhance the ability to tailor the energy density of sodium–oxygen batteries (NaO(2): 1071 Wh kg(−1) and Na(2)O(2): 1505 Wh kg(−1)). Through spectroelectrochemical analysis of a range of non‐aqueous solvents, we describe the dependence of these processes on the electrolyte solvent and subsequent interactions formed between Na(+) and O(2) (−). The solvents ability to form and remove [Na(+)‐O(2) (−)](ads) based on Gutmann donor number influences the final discharge product and mechanism of the cell. Utilizing surface‐enhanced Raman spectroscopy and electrochemical techniques, we demonstrate an analysis of the response of Na‐O(2) cell chemistry with sulfoxide, amide, ether, and nitrile electrolyte solvents.