Synthesis and electrochemical characterization of PEO-based polymer electrolytes with room temperature ionic liquids

New gel polymer electrolytes containing 1-butyl-4-methylpyridinium bis(trifluoromethanesulfonyl)imide (BMPyTFSI) ionic liquid are prepared by solution casting method. Thermal and electrochemical properties have been determined for these gel polymer electrolytes. The addition of BMPyTFSI to the P(EO)₂₀LiTFSI electrolyte results in an increase of the ionic conductivity, and at high BMPyTFSI concentration (BMPy⁺/Li⁺ = 1.0), the ionic conductivity reaches the value of 6.9 × 10⁻⁴ S/cm at 40 °C. The lithium ion transference numbers obtained from polarization measurements at 40 °C were found to decrease as the amount of BMPyTFSI increased. However, the lithium ionic conductivity increased with the content of BMPyTFSI. The electrochemical stability and interfacial stability for these gel polymer electrolytes were significantly improved due to the incorporation of BMPyTFSI.     

超低功耗的锂电池管理系统设计

为了满足某微功耗仪表的应用,提高安全性能,提出了一种超低功耗锂电池管理系统的设计方案。该方案采用双向高端微电流检测电路,结合开路电压和电荷积分算法实现电量检测。采用纽扣电池代替DC/DC降压电路最大程度降低功耗。系统实现了基本保护、剩余电量检测、故障记录等功能。该锂电池管理系统在仪表上进行验证,结果表明具有良好的稳定性和可靠性,平均工作电流仅145μA。     

商业化的锂离子电池石墨负极材料的研究进展

综述了锂离子电池石墨负极材料的研究进展,对MCMB、天然石墨与人造石墨、炭纤维为代表的石墨负极材料目前的研究和应用现状进行了详细的论述,并对石墨类炭负极的发展作了展望。     

基于MG811探头的二氧化碳采集系统设计

二氧化碳采集系统以德州仪器公司的MSP430F169为主要控制芯片,采用MG811二氧化碳气体感应探头检测二氧化碳气体浓度。通过HT1621来驱动段式LCD,显示测量的二氧化碳浓度数据,系统外扩M25P80芯片,实现对测量数据的存储,并可通过USB与上位机进行通信。实验证明,该系统设计工作稳定、结构简单、便于携带,有良好的推广前景。     

Studies of structure and cycleability of LiMn2O4 and LiNd0.01Mn1.99O4 as cathode for Li-ion batteries

Lithium manganese oxides LiMn₂O₄ and rare earth elements doped LiNd_0.01Mn_1.99O₄ were synthesized by microwave method. The structure and the electrochemical performances of the samples were characterized. XRD data shows both samples exhibit the same pure spinel phase. But due to the introduction of Nd³⁺ ion into the unit cell, the lattice parameter of the Nd-doped spinel was larger than that of the undoped one. The two samples had a similar morphology including small particle size and homogeneous particle distribution as tested by SEM. The cyclic voltammmetry and constant-current charge-discharge tested that Nd-doped spinel displayed a better reversibility and cycleability.     

A study on capacity fading of lithium-ion battery with manganese spinel positive electrode during cycling

The capacity fading mechanism of lithium-ion cell was studied by disassembling the charge-discharged cells and analyzing their electrodes using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS), etc. Cu ion dissolved from current collector of anode and Mn ion dissolved from LiMn₂O₄ spinel (cathode) were all existing in solid electrolyte interface (SEI) layer on carbon anode as Cu₂O and MnO or MnO₂, respectively. These depositions of Cu and Mn oxides did not uniformly deposited on the anode side, and most of them were detected on the carbon surface nearby to the separator side. The SEI layer is hard and about 0.3 μm in thickness. Furthermore, the cycling performance of the cells can be improved by adding 1,2,3-benzotrazole (a corrosion inhibitor of Cu) before assembling the cell, it then coordinates strongly with Cu ions into the electrolyte. From the results, it is obvious that the existing of Cu oxide as well as Mn oxide in the SEI layer, which blocks the normal intercalation of the lithium ions, is one of the factors for the capacity fading of the cells.     

Effect of structural and electrochemical properties of different Cr-doped contents of Li[Ni1/3Mn1/3Co1/3]O2

Layered Li[Ni_(1−x)/3Mn_(1−x)/3Co_(1−x)/3Cr_x]O₂ materials with x = 0, 0.01, 0.02, 0.03, 0.05 are prepared by a solid-state pyrolysis method. The oxide compounds were calcined with various Cr-doped contents, which result in greater difference in morphological (shape, particle size and specific surface area) and the electrochemical (first charge profile, reversible capacity and rate capability) differences. The Li[Ni_(1−x)/3Mn_(1−x)/3Co_(1−x)/3Cr_x]O₂ powders were characterized by means of X-ray diffraction (XRD), charge/discharge cycling, cyclic voltammetry, and SEM. XRD experiment revealed that the Li[Ni_(1−x)/3Mn_(1−x)/3Co_(1−x)/3Cr_x]O₂ (x = 0, 0.01, 0.02, 0.03, 0.05) were crystallized to well layered -NaFeO₂ structure. The first specific discharge capacity and coulombic efficiency of the electrode of Cr-doped materials were higher than that of pristine material. When x = 0.02, the sample showed the highest first discharge capacity of 241.9 mAh g⁻¹ at a current density of 30 mA g⁻¹ in the voltage range 2.3–4.6 V, and the Cr-doped samples exhibited higher discharge capacity and better cycleability under medium and high current densities at room temperature.     

An electrochemical impedance spectroscopy and scanning electron microscopy study of the influence of positive plate compression on the electrochemical behaviour of lead-acid batteries

This study has developed an electrochemical impedance spectroscopy (EIS) method for the in situ investigation of the influence of positive plate compression on the electrochemical behaviour of lead-acid batteries during charge/discharge cycling. The EIS data for a fully charged and fully discharged battery are internally consistent with the expected kinetics of a battery in the opposite states of charge, and demonstrate that EIS measurements may be recorded with a high level of reproducibility. Furthermore, this study has necessitated the development of a special cell incorporating horizontally orientated battery plates that can be subjected to elevated pressure through the stacking of lead bricks on top of the cell, as well as a physically robust reference electrode system that can withstand the application of pressure. For this purpose, a platinum-wire pseudo-reference electrode has been developed, and has been shown to exhibit sufficient electrode stability over the period of an EIS recording, enabling the measurement of reproducible and meaningful EIS data. Additionally, the influence of positive plate compression on the behaviour of the lead-acid battery has been investigated by using scanning electron microscopy (SEM). Clearly, the experimental data show that plate compression enhances significantly the kinetics and concomitant performance of the lead-acid battery, and this is related to the enhanced reactivity of the active material, as rationalized by using the agglomeration-of-spheres (AOS) model.     

Lithium-deficient LiYMn2O4 spinels (0.9 ≤ Y < 1): Lithium content, synthesis temperature, thermal behaviour and electrochemical properties

Lithium-deficient Li_YMn₂O₄ spinels (LD-Li_YMn₂O₄) with nominal composition (0.9 ≤ Y < 1) have been synthesized by melt impregnation from Mn₂O₃ and LiNO₃ at temperatures ranging from 700 °C to 850 °C. X-ray diffraction data show that LD-Li_YMn₂O₄ spinels are obtained as single phases in the range Y = 0.975-1 at 700 °C and 750 °C. Morphological characterization by transmission electron microscopy shows that the particle size of LD-Li_YMn₂O₄ spinels increases on decreasing the Li-content. The influence of the Li-content and the synthesis temperature on the thermal and electrochemical behaviours has been systematically studied. Thermal analysis studies indicate that the temperature of the first thermal effect in the differential thermal analysis (DTA)/thermogravimetric (TG) curves, T_C1, linearly increases on decreasing the Li-content. The electrochemical properties of LD-Li_YMn₂O₄ spinels, determined by galvanostatic cycling, notably change with the synthesis conditions. So, the first discharge capacity, Q_disch., at C rate increases on rising the Li-content and the synthesis temperature. The sample Li_0.975Mn₂O₄ synthesized at 700 °C has a Q_disch. = 123 mAh g⁻¹ and a capacity retention of 99.77% per cycle. This LD-Li_YMn₂O₄ sample had the best electrochemical characteristics of the series.     

The influence of preparation conditions on electrochemical properties of LiNi0.5Mn1.5O4 thin film electrodes by PLD

LiNi_0.5Mn_1.5O₄ thin films were prepared by pulsed laser deposition (PLD) on stainless steel substrates. The growth of the films has been studied as a function of substrate temperature and oxygen partial pressure in deposition, using X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM). Electrochemical properties of LiNi_0.5Mn_1.5O₄ thin film cathodes were investigated using cyclic voltammetry and galvanostatic charge/discharge against a lithium anode. The initial capacity and capacity retention of the films are highly dependent on the crystallinity and purity of the films. LiNi_0.5Mn_1.5O₄ thin films grown at 600 °C in an oxygen partial pressure of 200 mTorr are well crystallized with high purity, exhibiting excellent capacity retention between 3 and 5 V with a LiPF₆-based electrolyte.