阳极
法拉第效率
电化学
介电谱
扩散
循环伏安法
分析化学(期刊)
电极
离子
空位缺陷
化学
电池(电)
材料科学
电流密度
热力学
物理化学
色谱法
有机化学
物理
功率(物理)
量子力学
结晶学
作者
Mahesh Chandra,Tuhin Suvra Khan,Rishabh Shukla,Salahuddin Ahamad,Amit Gupta,Suddhasatwa Basu,M. Ali Haider,R. S. Dhaka
标识
DOI:10.1016/j.electacta.2019.135293
摘要
Abstract We study Na/Li–ion diffusion and electrochemical performance of NaVO3 (NVO) as anode material in Na/Li–ion batteries with the specific capacity of ≈350 mAhg−1 at the current density 11 mAg−1 after 300 cycles for Li-ion battery. Remarkably, the capacity retains ≥200 mAhg−1 even after 400 cycles at 44 mAg−1 with Coulombic efficiency >99%. The deduced diffusion coefficient from galvanostatic intermittent titration technique (GITT), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) measurements for NVO as anode in Li–ion battery is in the range of 10−10–10−12 cm2s−1. In case of Na-ion batteries, the NVO electrode exhibits initial capacity of 385 mAhg−1 at 7 mAg−1 current rate, but the capacity degradation is relatively faster in subsequent cycles. We find the diffusion coefficient of NVO–Na cells similar to that of NVO–Li. On the other hand, our charge discharge measurements suggest that the overall performance of NVO anode is better in Li–ion battery than Na-ion. Moreover, we use the density functional theory to simulate the energetics of Na vacancy formation or addition in the bulk of the NVO structure, which is found to be 0.9–1.2 eV higher than that of the most stable (100) surface. Thus, the Na ion incorporation at the surface of the electrode material is more facile compared to the bulk.
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