循环伏安法
熔盐
计时安培法
无机化学
电解质
参比电极
过电位
介电谱
化学
电化学
电极
氧化还原
碘化物
氢醌电极
工作电极
材料科学
物理化学
作者
Adam Maraschky,Stephen Percival,Rose Lee,Melissa Meyerson,Amanda S. Peretti,Erik David Spoerke,Leo J. Small
标识
DOI:10.1149/1945-7111/acd874
摘要
Iodide redox reactions in molten NaI/AlCl 3 are shown to generate surface-blocking films, which may limit the useful cycling rates and energy densities of molten sodium batteries below 150 °C. An experimental investigation of electrode interfacial stability at 110 °C reveals the source of the reaction rate limitations. Electrochemical experiments in a 3-electrode configuration confirm an increase of resistance on the electrode surface after oxidation or reduction current is passed. Using chronopotentiometry, chronoamperometry, cyclic voltammetry, and electrochemical impedance spectroscopy, the film formation is shown to depend on the electrode material (W, Mo, Ta, or glassy carbon), as well as the Lewis acidity and molar ratio of I − /I 3 − in the molten salt electrolytes. These factors impact the amount of charge that can be passed at a given current density prior to developing excessive overpotential due to film formation that blocks the electrode surface. The results presented here guide the design and use of iodide-based molten salt electrolytes and electrode materials for grid scale battery applications.
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