Electrochemical studies and diffusion kinetics in the Chevrel phase (Mo6S8) for rechargeable Mg batteries

IF 3.1 3区 物理与天体物理 Q2 PHYSICS, APPLIED Journal of Physics D: Applied Physics Pub Date : 2024-09-10 DOI:10.1088/1361-6463/ad703a
Gazal Gupta, Raghvendra Gupta, Amit Gupta and Deepak Kumar
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Abstract

Based on its availability, cost and stability, rechargeable Mg batteries (RMBs) are potential candidates to fulfill the futuristic demand for high energy density storage devices. However, they are minimally explored due to sluggish Mg ion diffusion in cathode materials. Literature suggests that the Chevrel phase (CP) (Mo6S8) holds promise as a cathode (positive electrode) for RMBs due to its open structure and self-healing properties during cycling. This study reports the electrochemical performance of Mo6S8 (synthesized using cost effective precursors (Cu–Mo–MoS2)) as a cathode for RMBs for the first time. The development of Mo6S8 is a two-step process: (i) synthesis of Cu2Mo6S8 via high energy milling method using Cu, Mo and MoS2 as precursors and (ii) leaching of Cu from Cu2Mo6S8. The morphological and structural characteristics of the developed materials are recorded using x-ray diffraction and field emission scanning electron microscopy. The developed Mo6S8 is cuboid-shaped with a rhombohedral unit cell. To record the electrochemical performance of Mo6S8 as a positive electrode for rechargeable Mg batteries (RMBs), CR2016 type half-cells are fabricated. It is observed that the initial discharge capacity was 89 mA h g−1 at a current density of 25 mA g−1 (1C = 128 mA g−1). Interestingly, the capacity increases from 89 to ≈100 mA h g−1 during 50 cycles which is higher than reported in the literature. The coulombic efficiency (CE) of ≈90% is observed for 100 cycles. Additionally, the over-potential decreases with an increase in cycle number. Importantly, the authors explained the diffusion behavior of Mg ions in Mo6S8 with 0.4 M 2(PhMgCl)-AlCl3/THF (APC) electrolyte via cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic intermittent titration (GITT) technique. The diffusion coefficients have been calculated and fall in the range of 10−8−10−14 cm2 s−1. Also, the authors explain the effect of outer site activation during cycling on the diffusion kinetics of the materials using the GITT technique. This investigation of diffusion kinetics of Mg ions in Mo6S8 may pave the way for evaluating various CPs as electrode materials for future rechargeable magnesium battery systems.
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用于可充电镁电池的 Chevrel 相(Mo6S8)的电化学研究和扩散动力学
可充电镁电池(RMB)具有易得性、成本低和稳定性等优点,是满足未来对高能量密度存储设备需求的潜在候选材料。然而,由于镁离子在阴极材料中扩散缓慢,对它们的研究还很少。文献表明,Chevrel 相(CP)(Mo6S8)因其开放式结构和循环过程中的自修复特性,有望成为人民币的阴极(正极)。本研究首次报道了作为人民币阴极的 Mo6S8(使用成本低廉的前驱体(Cu-Mo-MoS2)合成)的电化学性能。Mo6S8 的开发分为两步:(i) 以 Cu、Mo 和 MoS2 为前驱体,通过高能研磨法合成 Cu2Mo6S8;(ii) 从 Cu2Mo6S8 中浸出 Cu。利用 X 射线衍射和场发射扫描电子显微镜记录了所开发材料的形态和结构特征。所开发的 Mo6S8 呈立方体状,具有斜方体单胞。为了记录作为可充电镁电池(RMB)正极的 Mo6S8 的电化学性能,制作了 CR2016 型半电池。据观察,在电流密度为 25 mA g-1 (1C = 128 mA g-1)时,初始放电容量为 89 mA h g-1。有趣的是,在 50 个循环期间,容量从 89 mA h g-1 增加到 ≈100 mA h g-1,高于文献报道的水平。循环 100 次后,库仑效率(CE)≈90%。此外,过电位随着循环次数的增加而降低。重要的是,作者通过循环伏安法、电化学阻抗光谱法和电静电间歇滴定(GITT)技术解释了镁离子在 0.4 M 2(PhMgCl)-AlCl3/THF (APC) 电解质的 Mo6S8 中的扩散行为。计算得出的扩散系数在 10-8-10-14 cm2 s-1 之间。此外,作者还利用 GITT 技术解释了循环过程中外位点活化对材料扩散动力学的影响。这项关于镁离子在 Mo6S8 中扩散动力学的研究可能会为评估各种氯化石蜡作为未来可充电镁电池系统的电极材料铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Physics D: Applied Physics
Journal of Physics D: Applied Physics 物理-物理:应用
CiteScore
6.80
自引率
8.80%
发文量
835
审稿时长
2.1 months
期刊介绍: This journal is concerned with all aspects of applied physics research, from biophysics, magnetism, plasmas and semiconductors to the structure and properties of matter.
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