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71.
模糊控制技术在电池快速充电控制中的应用 总被引:1,自引:0,他引:1
曹建平 《南京工业职业技术学院学报》2010,10(2):1-3
针对常规的电池快速充电模式存在的问题,探讨了基于模糊控制技术的电池快速充电器的设计方法,给出了该方案应用的测试结果,实现了电池充电过程的优化控制,为有效延长电池的使用寿命提供了一种解决方案。 相似文献
72.
73.
Yong Min Lee 《Electrochimica acta》2006,52(4):1582-1587
Highly ion-conductive solid polymer electrolyte (SPE) based on polyethylene (PE) non-woven matrix is prepared by filling poly(ethylene glycol) (PEG)-based crosslinked electrolyte inside the pores of the non-woven matrix. The PE non-woven matrix not only shows good mechanical strength for SPE to be a free-standing film, but also has very porous structure for high ion conductivity. The ion conductivity of SPE based on PE non-woven matrix can be enhanced by adding sufficient non-volatile plasticizer such as poly(ethylene glycol) dimethyl ether (PEGDME) into ion conduction phase without sacrificing mechanical strength. SPE with 20 wt.% crosslinking agent and 80 wt.% non-volatile plasticizer shows 3.1 × 10−4 S cm−1 at room temperature (20 °C), to our knowledge, which is the highest level for SPEs. It is also electrochemically stable up to 5.2 V and has high transference number about 0.52 due to the introduction of anion receptor as an additive. The interfacial resistance between Li electrode and SPE is low enough to perform charge/discharge test of unit cell consisting of LiCoO2/SPE/Li at room temperature. The discharge capacity of the unit cell shows 87% of theoretical value with 86% Coulombic efficiency. 相似文献
74.
Jernej Drofenik Robert Dominko Mogens Mogensen Stane Pejovnik 《Electrochimica acta》2003,48(7):883-889
Four types of cellulose, in particular carboxy methyl cellulose (CMC), are tested as potential binding materials in graphitic anodes for lithium ion batteries. It is shown that a minimum content of a cellulose which gives acceptable anode properties (reversible capacity>300 mA h g−1 during the first 10 cycles, irreversible loss<20%) is about 2 wt.%, which is less than in the case of conventional polymeric binders (5-10 wt.%). Kinetics of insertion-deinsertion and passivation processes seem not to be affected by the presence of cellulose. Explanation for the electrode failure at cellulose contents lower than 1 wt.% is given based on X-ray diffraction and microscopy investigations. Finally, the structure (distribution) of cellulose in the composite anode material is discussed and (indirectly) checked with a series of experiments. Most results are compared with the corresponding results obtained either with gelatin or conventional polymeric binders or both. 相似文献
75.
The impedance rise that results from the accelerated aging of high-power lithium-ion cells containing LiNi0.8Co0.15Al0.05O2-based positive and graphite-based negative electrodes is dominated by contributions from the positive electrode. Data from various diagnostic experiments have indicated that a general degradation of the ionic pathway, apparently caused by surface film formation on the oxide particles, produces the positive electrode interface rise. One mechanistic hypothesis postulates that these surface films are components of the negative electrode solid electrolyte interphase (SEI) layer that migrate through the electrolyte and separator and subsequently coat the positive electrode. This hypothesis is examined in this article by subjecting cells with LiNi0.8Co0.15Al0.05O2-based positive and Li4/3Ti5/3O4-based negative electrodes to accelerated aging. The impedance rise in these cells was observed to be almost entirely from the positive electrode. Because reduction products are not expected on the 1.55 V Li4/3Ti5/3O4 electrode, the positive electrode impedance cannot be attributed to the migration of SEI-type fragments from the negative electrode. It follows then that the impedance rise results from mechanisms that are “intrinsic” to the positive electrode. 相似文献
76.
A method has been developed to suppress the decomposition of propylene carbonate (PC) by coating graphite electrode foil with a layer of silver. Results from electrochemical impedance measurements show that the Ag-coated graphite electrode presents lower charge transfer resistance and faster diffusion of lithium ions in comparison with the virginal one. Cyclic voltammograms and discharge-charge measurements suggest that the decomposition of propylene carbonate and co-intercalation of solvated lithium ions are prevented, and lithium ions can reversibly intercalate into and deintercalate from the Ag-coated graphite electrode. These results indicate that Ag-coating is a good way to improve the electrochemical performance of graphitic carbon in PC-based electrolyte solutions. 相似文献
77.
水溶性有机液流电池自2014年出现后发展迅猛,特别是近些年来有机电活性物质的降解和二聚导致的容量衰减问题得到初步解决后,该类液流电池有望作为大规模储能系统的候选者。然而能量密度较低的问题限制了其商业化的进程。对此,主要从增大溶解度、提高电化学窗口和电子的得失数这3个方面详细介绍了5种提高水溶性有机液流电池能量密度的方法——分子结构剪裁、“interaction-mediating”策略的应用、采用聚合物电活性物质、“氧化还原靶向”原理和电极表面的改性,同时对进一步提高水溶性有机液流电池能量密度的策略进行了简要展望。 相似文献
78.
Summary: This paper introduces a new inorganic poly(phosphazene disulfide) material. With unique element composition and molecular structure, the polymer has noncombustible safety and preferable conductivity. When used as cathode material for rechargeable lithium batteries, the polymer's first discharge capacity is as high as 467.9 mAh · g?1, which can be retained at 409.9 mAh · g?1 after 60 repeated cycles. Therefore, it has a great application potential in the field of lithium batteries.
79.
以聚吡咯(PVP K60)为表面活性剂和碳源,采用流变相法合成了x Li Fe PO4·y Li3V2(PO4)3/C正极材料样品。利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)对样品形貌和结构进行了测试;采用电池测试仪和电化学工作站对样品电化学性能进行了测试,分析了不同复合比(x:y)对其结构和电化学性能的影响。研究表明:复合材料中存在两相复合与元素掺杂两种效应;当复合比为5∶1时材料的电化学性能最优,在0.1和10 C倍率下放电容量分别达到162.7和104.6 m Ah·g-1,且具有良好的循环稳定性。 相似文献
80.
以Mn3O4为锰源,采用固相反应法,在较低的温度(650℃)制得尖晶石LiMn2O4正极材料。采用X射线衍射(XRD)、扫描电镜(SEM)、循环伏安和恒流充放电等技术对其相组成、微结构和电化学性能进行表征。结果表明该正极材料结晶良好,一次粒径约为150 nm。它的电化学性能,尤其是循环性能,明显优越于在较高温度合成的LiMn2O4。在电流密度为74 mA?g-1时,测得比容量为128 mAh?g-1,在1 480 mA?g-1时,比容量为105 mAh?g-1;在室温、148 mA?g-1充放电200次循环后,容量保持率为93%。 相似文献