Le Calvez Etienne, Espinosa-Angeles Julio César, Whang Grace J, Dupré Nicolas, Dunn Bruce S, Crosnier Olivier, Brousse Thierry
Nantes Université, CNRS, Institut des Matériaux de Nantes Jean Rouxel, IMN, Nantes, France.
Réseau sur le Stockage Electrochimique de l'Energie (RS2E), CNRS FR 3459, Amiens Cedex, France.
Front Chem. 2022 Apr 13;10:873783. doi: 10.3389/fchem.2022.873783. eCollection 2022.
The broader development of the electric car for tomorrow's mobility requires the emergence of new fast-charging negative electrode materials to replace graphite in Li-ion batteries. In this area, the design of new compounds using innovative approaches could be the key to discovering new negative electrode materials that allow for faster charging and discharging processes. Here, we present a partially substituted AgNbO perovskite material by introducing lanthanum in the A-site. By creating two vacancies for every lanthanum introduced in the structure, the resulting general formula becomes AgLa□NbO (with x ≤ 0.20 and where □ is a A-site vacancy), allowing the insertion of lithium ions. The highly substituted AgLa□NbO oxide shows a specific capacity of 40 mAh.g at a low sweep rate (0.1 mV s). Interestingly, AgLa□NbO retains 64% of its capacity at a very high sweep rate (50 mV s) and about 95% after 800 cycles. Li MAS NMR experiments confirmed the insertion of lithium ions in these materials. A kinetic analysis of AgLa□NbO underlines the ability to store charge without solid-state ion-diffusion limitations. Furthermore, XRD indicates no structural modification of the compound when accommodating lithium ions, which can be considered as zero-strain material. This finding explains the interesting capacity retention observed after 800 cycles. This paper thus demonstrates an alternative approach to traditional insertion materials and identifies a different way to explore not-so common electrode materials for fast energy storage application.
为了满足未来出行对电动汽车的广泛需求,需要研发新型快速充电负极材料来取代锂离子电池中的石墨。在这一领域,采用创新方法设计新化合物可能是发现新型负极材料的关键,这些材料能够实现更快的充放电过程。在此,我们通过在A位引入镧元素,展示了一种部分取代的AgNbO钙钛矿材料。通过在结构中每引入一个镧原子就创造两个空位,得到的通式变为AgLa□NbO(x≤0.20,□表示A位空位),从而允许锂离子嵌入。高度取代的AgLa□NbO氧化物在低扫描速率(0.1 mV s)下表现出40 mAh·g的比容量。有趣的是,AgLa□NbO在非常高的扫描速率(50 mV s)下仍保留其容量的64%,在800次循环后约保留95%。Li MAS NMR实验证实了锂离子在这些材料中的嵌入。对AgLa□NbO的动力学分析强调了其在无固态离子扩散限制的情况下存储电荷的能力。此外,XRD表明该化合物在容纳锂离子时没有结构变化,可被视为零应变材料。这一发现解释了在800次循环后观察到的有趣的容量保持现象。因此,本文展示了一种不同于传统嵌入材料的方法,并确定了一种探索用于快速储能应用的不常见电极材料的不同途径。