镁离子电池负极材料TiO2的制备及电化学表征

A. Abildina, Kh. Avchukir, R. Dzhumanova, A. Beiseyeva, G. Rakhymbay, A. Argimbayeva
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引用次数: 1

摘要

在二氧化钛粉的基础上制备阳极。利用椭偏仪、扫描电镜(SEM)、x射线能谱仪(EDS)和x射线衍射仪(XRD)研究了其形貌特征。并用循环伏安法研究了其电化学性能。分散、混合初始试剂以获得均匀的浆料及其涂层到衬底上、干燥和切割电极是阳极生产的主要步骤。椭偏仪、扫描电镜和能谱分析结果表明,该层厚度约为200 μm,呈均匀分布的多孔结构,颗粒直径为50 ~ 80 nm,二氧化钛含量为45.7%。XRD数据证实,活性阳极基体的形成具有单斜晶格,对应于二氧化钛(B)改性后含有少量锐钛矿夹杂物。研究了电极在乙腈基Mg(TFSI)2溶液中的电化学行为。扩散系数(DMg)和电荷转移速率常数(kct)分别由循环伏安图1.54∙10-2 cm2/s和1.29∙10-4 cm/s测定。在不同的循环次数下,阴极和阳极过程的电量消耗比揭示了两步电化学反应。循环伏安图计算的极化电阻(Rp)值较小,表明插入/脱插过程中镁离子的快速扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and electrochemical characterization of TiO2 as an anode material for magnesium-ion batteries
Anode on the basis of titanium dioxide powder was made. Its morphological characteristics were investigated using ellipsometry, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). Electrochemical properties were also investigated by cyclic voltammetry. Dispersing, mixing the initial reagents for obtaining homogenized paste and its coating to a substrate, drying and cutting the electrodes were main steps of anode production. The results of ellipsometry, SEM and EDS demonstrated a uniformly distributed layer of about 200 μm thickness with porous structure, particle diameter of 50–80 nm and titanium dioxide content (45.7 %). The XRD data confirmed the active anode matrix formation with a monoclinic crystal lattice corresponding to the modification of titanium dioxide (B) with small anatase inclusions. Electrochemical behavior of the electrode was examined in acetonitrile-based Mg(TFSI)2 solution. Diffusion coefficient (DMg) and the charge transfer rate constant (kct) were determined from cyclic voltammograms 1.54∙10–2 cm2/s and 1.29∙10–4 cm/s, respectively. A two-step electrochemical reaction was revealed by the ratio of the electricity amount consumed in the cathode and anode processes at varying the number of cycles. Small values of polarization resistance (Rp) calculated from cyclic voltammograms indicated rapid diffusion of magnesium ions during intercalation/deintercalation.
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