Metin Orbay, Abbas Khan, Olivier Crosnier, Thierry Brousse, Andrea Balducci
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引用次数: 0
Abstract
In this work, we report on the investigation the perovskite-type AgNbO3 as a model negative electrode for sodium and potassium systems. We demonstrated that during the initial discharge, regardless of the inserted cation, the material undergoes an activation mechanism that induces a crystalline-to-amorphous transition. This transition, in turn, leads to an enhancement of the electrode capacity. At 5 A g−1 sodium-ion AgNbO3 and Potassium-ion AgNbO3 display capacities of 81 mAh g−1 and 60 mAh g−1, respectively. Furthermore, both electrodes display good cycling stability and efficiency over 350 cycles at 1 A g−1.
在这项工作中,我们报道了钙钛矿型AgNbO3作为钠和钾系统的模型负极的研究。我们证明了在初始放电过程中,无论插入的阳离子如何,材料都经历了一个激活机制,诱导了晶体到非晶态的转变。这种转变反过来又导致电极容量的增强。在5 Ag−1时,钠离子AgNbO3和钾离子AgNbO3的容量分别为81 mAh g−1和60 mAh g−1。此外,两种电极在1 A g−1下的350次循环中都表现出良好的循环稳定性和效率。
期刊介绍:
Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.