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The sodium intercalation compound , more commonly , was studied as a potential positive electrode in an aqueous electrolyte hybrid energy storage device. Varying ratios of precursors were used in a solid-state synthetic route in an effort to compensate for volatile loss of sodium during processing. The powders were characterized using X-ray powder diffraction and thermogravimetric analysis, while particle morphology and formation were studied by scanning electron microscopy/electron dispersive spectroscopy and transmission electron microscopy. Electrochemical behavior was characterized by galvanostatic cycling and cyclic voltammetry. With a positive electrode voltage window of −0.3 to 0.3 V vs a reference electrode, a specific capacity of 35 mAh/g was observed after 20 cycles at a C/1.4 rate (25 mA/g) with little capacity loss. The most stable of the materials were made with a Na:Mn precursor ratio equal to 0.55 and showed excellent performance through many charge/discharge cycles. These samples also contained varying amounts of and impurity phases. The results indicated a relationship between the precursor Na/Mn ratio and the resultant redox potentials associated with the multiple hybrid Mn oxidation states encountered during cycling although no significant variance in the crystallography of the phase was observed.
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Amul Tevar
Carnegie Mellon University
Jay Whitacre
Aquion (Czechia)
Journal of The Electrochemical Society
Carnegie Mellon University
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Tevar et al. (Fri,) studied this question.
synapsesocial.com/papers/69d9e0ab00ab073a278377c6 — DOI: https://doi.org/10.1149/1.3428667
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