Zhang Qing, Bruck Andrea M, Bock David C, Li Jing, Sarbada Varun, Hull Robert, Stach Eric A, Takeuchi Kenneth J, Takeuchi Esther S, Marschilok Amy C
Department of Materials Science and Engineering, Stony Brook University, Stony Brook, NY 11794, USA.
Phys Chem Chem Phys. 2017 May 31;19(21):14160-14169. doi: 10.1039/c7cp02239e.
LiVO (n = 0-0.2) has been extensively investigated as a cathode material for Li ion batteries because of its superior electrochemical properties including high specific energy and good rate capability. In this paper, a synchrotron based energy dispersive X-ray diffraction (EDXRD) technique was employed to profile the phase transitions and the spatial phase distribution of a LiVO electrode during electrochemical (de)lithiation in situ and operando. As annealing temperature during the preparation of the LiVO material has a strong influence on the morphology and crystallinity, and consequently influences the electrochemical outcomes of the material, LiVO materials prepared at two different temperatures, 500 and 300 °C (LVO500 and LVO300), were employed in this study. The EDXRD spectra of LVO500 and LVO300 cells pre-discharged at C/18, C/40 and C/150 were recorded in situ, and phase localization and relative intensity of the peaks were compared. For cells discharged at the C/18 rate, although α and β phases were distributed uniformly within the LVO500 electrode, they were localized on two sides of the LVO300 electrode. Discharging rates of C/40 and C/150 led to homogeneous β phase formation in both LVO500 and LVO300 electrodes. Furthermore, the phase distribution as a function of position and (de)lithiation extent was mapped operando as the LVO500 cell was (de)lithiated. The operando data indicate that (1) the lithiation reaction initiated from the side of the electrode facing the Li anode and proceeded towards the side facing the steel can, (2) during discharge the phase transformation from a Li-poor to a Li-rich α phase and the formation of a β phase can proceed simultaneously in the electrode after the first formation of a β phase, and (3) the structural evolution occurring during charging is not the reverse of that during discharge and takes place homogenously throughout the electrode.
由于LiVO(n = 0 - 0.2)具有包括高比能量和良好倍率性能在内的优异电化学性能,它作为锂离子电池的正极材料已得到广泛研究。在本文中,采用基于同步加速器的能量色散X射线衍射(EDXRD)技术,对LiVO电极在电化学(脱)锂过程中的相变和空间相分布进行原位和实时监测。由于LiVO材料制备过程中的退火温度对其形态和结晶度有很大影响,进而影响材料的电化学性能,因此本研究采用在500和300 °C两个不同温度下制备的LiVO材料(LVO500和LVO300)。原位记录了在C/18、C/40和C/150下预放电的LVO500和LVO300电池的EDXRD光谱,并比较了峰的相定位和相对强度。对于以C/18速率放电的电池,尽管α相和β相在LVO500电极内均匀分布,但它们在LVO300电极的两侧局部化。C/40和C/150的放电速率导致LVO500和LVO300电极中均形成均匀的β相。此外,在LVO500电池进行(脱)锂时,实时绘制了作为位置和(脱)锂程度函数的相分布图。实时数据表明:(1)锂化反应从电极面向锂阳极的一侧开始,并朝着面向钢壳的一侧进行;(2)在放电过程中,在首次形成β相后,电极中从贫锂α相到富锂α相的相变和β相的形成可以同时进行;(3)充电过程中发生的结构演变与放电过程不同,且在整个电极中均匀发生。