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锂离子电池电解液过充添加剂的行为 总被引:4,自引:2,他引:4
制备了3种1 mol/L LiPF6电解液,溶剂组成分别为:1)碳酸乙烯酯,碳酸二甲酯和碳酸甲乙酯;2)碳酸乙烯酯,碳酸二甲酯,碳酸甲乙酯和4%联苯;3)碳酸乙烯酯,碳酸二甲酯,碳酸甲乙酯和4%环己基苯.采用线性电压扫描法、锂循环效率法、锂离子电池的循环性能法和3 C倍率过充的方法测试了联苯与环己基苯电解液过充添加剂的行为.结果表明:环己基苯是一种较实用的锂离子电池电解液过充添加剂,环己基苯的电化学稳定性比联苯的高,环已基苯的氧化电势为4.72 V(vs Li/Li ),联苯的为4.54 V(vs Li/Li );以1 mA电流循环20次后,联苯的铂电极锂循环效率为15.7%,环己基苯的为59.3%;锂离子电池以1 C循环150次后,环己基苯的容量保持率为88%,联苯的为76.3%.环己基苯与联苯添加剂都改善了锂离子电池的耐过充性能,且两者的效果十分接近. 相似文献
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采用DSC和XRD方法研究了1 mol.L-1 LiPF6电解液的热行为,发现EMC和H2O降低了1 mol.L-1 LiPF6电解液(溶剂为EC\DML,质量比为1:1)的热稳定性。电解液热分解反应是EMC分解生成DEC和DMC,而DEC和DMC与LiPF6的分解产物PF5发生系列化学反应,释放大量反应热与气体。由于可燃性电解液与Li0.5CoO2的热分解产物O2之间发生燃烧反应,使Li0.5CoO2发生复杂的热分解反应。高温下电解液与LiC6电极的热反应主要是:固体电解质膜(SEI膜)的碎裂反应,LiC6与粘结剂和电解液之间的反应。热反应主要发生在石墨的表面,而石墨的晶形结构在160℃热反应前后没有变化。 相似文献
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以硼酸、硅溶胶、片状石墨为原料,采用碳热还原法制备SiC-B_4C复合粉末。研究了反应温度对SiC-B_4C复合粉末的烧失率和物相组成的影响。采用X射线衍射仪(XRD)、激光粒度分析仪(LPSA)对实验样品的物相组成、粒度大小及其分布进行分析。结果表明:在反应温度达到1500℃以上时,采用碳热还原法可以成功合成出SiC-B_4C复合粉末。合成SiC-B_4C复合粉末的最适温度与硼酸用量有关。当硼酸用量为理论配比时,合成SiC-B_4C复合粉末的适宜反应温度为1500℃;当硼酸过量30%时,合成Si C-B_4C复合粉末的适宜反应温度为1550℃。当硼酸过量30%时,在1550°C下合成的SiC-B_4C复合粉末中位粒径为0.14μm。 相似文献
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为了降低镍氢电池的原材料成本 ,研究了一系列多元、低钴和无钴AB5型贮氢合金 ,以及取代元素对贮氢合金电化学性质的影响。结果显示 ,用少量的铁、铜和铬部分取代贮氢合金La(NiMnCoAl) 5中的钴对改善贮氢合金电化学循环稳定性有效。贮氢合金La(NiMnAl) 4.6(FeCuCr) 0 .2 Co0 .2 具有满意的循环稳定性 ,它在 0 .2C放电条件下的最大放电容量为 2 96mAh/g-1,经过 30 0次循环容量衰减仅 2 1.8%。另外 ,还用X射线衍射检测了贮氢合金的微观结构 相似文献
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Preparation of calcium stannate by modified wet chemical method 总被引:1,自引:2,他引:1
A modified wet chemical route for low-temperature synthesis of the calcium stannate CaSnO3, a potential material for dielectric applications is reported. Firstly, a precursor CaSn(OH)6 was prepared using tin tetrachloride, calcium chloride and sodium hydroxide at room temperature. Then the precursor was annealed at relatively low temperature of 600 ℃ to obtain CaSnO3. The phase identification, thermal behavior and surface morphology of the samples were characterized by element analysis, X-ray diffraction (XRD) , thermo-gravimetric (TG) analysis and derivative thermo-gravimetric (DTG) analysis, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) in detail. The results show that CaSnO3 obtained by this method possesses a cubic perovskite structure with average grain size of 5μm. 相似文献
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Li2Fe0.5Mn0.5SiO4 material was synthesized by a citric acid-assisted sol-gel method. The influence of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+) on the electrochemical properties of Li2Fe0.5Mn0.5SiO4 was studied. The final sample was identified as Li2Fe0.5Mn0.5SiO4 with a Pmn21 monoclinic structure by X-ray diffraction analysis. The crystal phases components and crystal phase structure of the Li2Fe0.5Mn0.4SiO4 material were improved as the increase of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+). Field-emission scanning electron microscopy verified that the Li2Fe0.5Mn0.5SiO4 particles are agglomerates of Li2Fe0.5Mn0.5SiO4 primary particles with a geometric mean diameter of 220 nm. The Li2Fe0.5Mn0.5SiO4 sample was used as an electrode material for rechargeable lithium ion batteries, and the electrochemical measurements were carried out at room temperature. The Li2Fe0.5Mn0.5SiO4 electrode delivered a first discharge capacity of 230.1 mAh/g at the current density of 10 mA/g in first cycle and about 162 mAh/g after 20 cycles at the current density of 20 mA/g. 相似文献
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