快离子导体
离子电导率
离子
电极
材料科学
尖晶石
电导率
离子半径
化学
重量分析
离子键合
分析化学(期刊)
无机化学
电解质
物理化学
冶金
色谱法
有机化学
作者
Danielle M. Butts,Jürgen Schoiber,Christopher Choi,Günther J. Redhammer,Nicola Hüsing,Scott W. Donne,Bruce Dunn
标识
DOI:10.1021/acs.chemmater.1c01680
摘要
The great interest in Na-ion batteries has led to the development of a number of materials based on the analogues of Li-ion battery materials. However, the larger ion radius and the lower operating potential of Na compared to those of Li show the limitation of that approach and underscore the need for new methods of electrode material design. In this paper, the well-known superionic conductor, Na β″-Al2O3, is converted into a high-rate Na+ negative electrode by substituting Fe for Al and achieving mixed electron–ion conduction; that is, the presence of Fe2+/Fe3+ in the spinel block of the structure produces electronic conduction, while Na+ transport is retained in the conduction plane. The 52 mol % Fe-substituted Na β″-Al2O3 exhibited a high ionic conductivity (∼10–3 S cm–1), near theoretical capacity values at 1C, and retained ∼70% of theoretical capacity at 20C. Kinetic analysis revealed that a surface-controlled charge-storage mechanism is responsible for the high-rate capability. Although the gravimetric capacity of this converted superionic conductor is limited by the small number of Na-ion storage sites available per transition metal, the transformation of Na β″-Al2O3 into a mixed electronic–ionic conducting electrode provides a set of design rules for achieving high-rate redox electrodes from solid-state electrolytes.
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