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1.
核壳结构三元锂离子电池正极材料研究进展   总被引:1,自引:1,他引:0  
李佳玮  厉英  孔亚州 《材料导报》2016,30(Z1):187-190
核壳结构三元锂离子电池正极材料由高比容量的内核与高稳定性的外壳组成,因其兼具容量高与循环稳定性好等优点,受到研究者与工业界的广泛关注。从三元壳核正极材料的结构类型和制备方法两方面进行综述,并对其商业化应用前景进行了展望和评价。  相似文献   

2.
李军  周燕  靳世东  郑育英 《材料导报》2011,25(9):51-53,67
球形化可以提高锂离子正极材料的压实密度、体积比容量并改善其加工性能和极片的质量。简要介绍了球形材料的特点,综述了球形LiCoO2、LiNixM1-xO2、LiMn2O4、LiFePO4等的制备及其性能,展望了球形正极材料的应用前景。  相似文献   

3.
锂离子电池正极材料热稳定性研究进展   总被引:1,自引:0,他引:1  
综述了锂离子电池正极材料热稳定性的研究现状及其进展。针对正极材料LiCcO2、LiNiO3、LiMn2O4及其衍生物的热稳定性,众多研究者提出了不同的反应机理,认为正极材料的热稳定性与颗粒大小、晶体结构、充/放电状态、脱锂程度及电解质性质等因素有关。可以利用掺杂技术、涂层技术及优化合成条件等手段来改善正极材料的热稳定性。  相似文献   

4.
锂离子电池正极材料LiFePO4的研究进展   总被引:1,自引:1,他引:1  
磷酸铁锂用作锂离子电池正极材料是当前研究热点之一,由于其性能、价格、安全和环境优势,其应用前景十分看好.首先对晶体结构进行了描述,并综述了近年来各种制备LiFePO4的方法,包括高温固相合成,机械化学法等"固相方法"以及溶胶-凝胶法等"软化学合成法",对各种方法的优缺点进行了分析对比.并且对LiFePO4的改性研究进行了简单的探讨.  相似文献   

5.
全固态薄膜锂离子电池正极材料研究进展   总被引:1,自引:0,他引:1  
全固态薄膜锂离子电池是锂离子电池的最新研究领域,正极材料的薄膜化成为锂离子电池的重要组成部分和研究热点.主要综述了LiCoO2、LiNiO2、LiMn2O4、v2O5、金属磷酸盐化合物等薄膜正极材料近几年来在材料改性、制备工艺等方面的研究状况,并展望了其发展趋势.  相似文献   

6.
王联  吴锋  吴川 《材料导报》2008,22(1):13-16
简要介绍了近年来磁控溅射和脉冲激光沉积制膜技术在薄膜型锂离子电池正极材料制备方面的应用研究; 对制膜新工艺及新型正极材料的研究现状进行了概括,认为现阶段新型材料LiFePO4有希望成为薄膜锂电池正极材料的首选,并展望了薄膜型锂离子电池的发展前景.  相似文献   

7.
对近年来圆外层状氧化锰锂正极材料的研究进展进行了综述。详细介绍了正交和单斜同质多晶层状氧化锰锂的晶体结构,合成方法及其电化学特性。开发新的合成方法以及多组分掺杂改性以提高英应用性仍是今后.层状氧化锰锂的研究发展方向。  相似文献   

8.
用单质硫和聚丙烯腈进行硫化,可以制备具有电化学活性的导电高分子材料硫化聚丙烯腈.这种材料用作锂离子电池正极活性材料,可以获得较高的比容量和较长的循环寿命.本文综述了硫化聚丙烯腈的研究进展和可能的储锂机理,并提出了进一步改进性能的方法.  相似文献   

9.
锂离子电池聚阴离子型硅酸盐正极材料的研究进展   总被引:1,自引:0,他引:1  
综述了硅酸盐正极材料的设计、特性、制备及电化学性能,介绍了基于密度泛函理论的量子化学计算在锂离子电池材料设计中的方法和理论,认为进一步开展Li2MSiO4及其复合材料的理论和实验研究可以获得性能优异的高容量正极材料.  相似文献   

10.
锂离子电池(LIB)近年来受到了广泛的关注,与其他可充电电池相比,锂离子电池LIB具有更高的能量密度、功率和效率.正极作为LIB的关键部件,其特性会显著影响LIB的性能.本文分类综述了一些锂离子正极材料,包括一元、二元、三元金属锂氧化物和磷酸亚铁锂正极材料,并对其优缺点进行了介绍.此外,本文还对已商业化的正极材料物性数...  相似文献   

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12.
锂金属电池被认为是最具潜力的高能量密度储能器件之一,但是锂金属电池负极低库仑效率及不可控的枝晶生长等问题阻碍了其商业化进程.在锂金属电池中,电解液会直接参与固态电解质界面膜(SEI)的形成,对锂金属负极的库仑效率、枝晶生长等产生重要影响.传统LiPF6基酯类电解液中,锂金属库仑效率低,且锂枝晶现象严重.近年来通过电解液添加剂、溶剂、锂盐以及锂盐浓度等途径调控电解液化学,在锂金属负极保护上取得了显著效果.例如,采用与锂金属负极兼容性更佳的醚类溶剂,可以降低电解液与锂金属的反应性;采用多种添加剂与新型锂盐复配可以有效抑制锂枝晶的形成;采用高浓度锂盐电解液,可以形成稳定SEI膜等.本文综述了锂枝晶的生长原理以及通过溶剂、锂盐、添加剂和高浓度电解液等策略调控电解液化学保护锂金属电池负极的研究现状,总结了各种途径的优势及局限性.并对锂金属电池电解液的发展提出了新的见解,以激发新的策略面对锂金属电池后续的挑战.  相似文献   

13.
Silicon-graphite composites were prepared by mechanical ball milling for 20 h under argon protection. The microstructure and electrochemical performance of the composites were characterized by X-ray diffraction (XRD), scanning electron microscopy, and electrochemical experiments. XRD showed that the materials prepared by ball milling were composites consisting of Si and graphite powders. The composite electrode showed the best performance, especially when annealed at 200 °C for 2 h, which had a reversible capacity of 595 mAh g−1 and an initial coulombic efficiency of 66%, and still retained 469 mAh g−1 after 40 cycles with about 0.6% capacity loss per cycle.  相似文献   

14.
Solid state battery (SSB) performance is largely governed by processes occurring at electrolyte–electrode interfaces. At the Li metal anode, where the overwhelming majority of solid electrolyte (SE) are unstable against Li metal, the interface can readily react to form emergent Li-solid electrolyte interphases (SEI) with ionic, electronic, chemical, mechanical, and electrochemical properties substantially distinct from the parent phase. Facing similar challenges with liquid electrolytes, the Li battery community underwent a half century-long effort, still in progress, to illuminate fundamental properties of the Li SEI—including chemistry, morphology, transport, and sources of Li loss upon cycling—from which guiding principles have emerged to drive improvement in electrolyte and interface design. The Li metal SEI with solid electrolytes presents both similarities and differences to that in liquid electrolytes, with differences defining unique research needs. Here, we examine current understanding of the Li-SE interface as well as learnings from the liquid electrolyte community that we propose might be adopted to help rationalize and improve SE integration with Li anodes. Through this lens, we inspect current state-of-understanding of Li SEI composition, structure, and properties, along with Coulombic efficiency values reported so far for Li cycling with SE. We also highlight potential Li modification strategies for SSB, which are informed by and exploit understanding of the ionic SEI phases; in some instances, engineering strategies utilize a liquid electrolyte SEI directly, making liquid-derived SEI knowledge of immediate relevance.  相似文献   

15.
P25/graphene nanocomposites were successful synthesized in a water-ethanol solvent under hydrothermal conditions. During the process of the reduction of GO into graphene (GR), the P25 nanoparticles were decorated on graphene sheets simultaneously. Moreover, the GR content in the as-synthesized nanocomposites can be easily adjusted by changing the dosage of P25. The interesting P25/GR nanocomposites were found to be a promising anode material for lithium-ion batteries and showed significantly enhanced Li-ion insertion/extraction performance. The optimal weight percentage of GR was found to be 29.9%, which resulted in a high capacity of 282.8 mAh g−1 after 50 cycles at a current rate of 0.5 C. The improved capacity may be attributed to the synergetic effect between graphene sheets and P25 nanoparticles.  相似文献   

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17.
电解质材料是锂离子电池的关键材料之一。LiBF4、双草酸硼酸锂(LiBOB)及草酸二氟硼酸锂(LiODFB)是极具应用前景的3种含硼锂盐。介绍了3种锂盐各自的优缺点及研究近况,重点综述了它们的离子传导特性及与电极材料的相容性能。  相似文献   

18.
采用热缩聚法(温度为420℃、反应时间为2 h)制备出碳纳米管/中间相炭微球复合材料。研究了碳纳米管添加量对中间相炭微球的形成和形貌的影响,以及对碳纳米管/中间相炭微球复合材料充放电性能的影响。实验结果表明,5%(质量分数)的碳纳米管添加量有利于中间相炭微球的形成,碳纳米管/中间相炭微球复合材料作为负极材料的锂离子电池充放电容量可达到337 mAh/g,20次循环后容量仍保持88%。  相似文献   

19.
Yu Zhang 《Materials Letters》2007,61(30):5209-5212
A new microporous carbon, prepared from pinecone hull, exhibits high charge/discharge capacity when used as anode material for lithium secondary batteries. After 6 cycling tests, the microporous carbon retains a discharge capacity of 357 mAh g− 1, and a coulombic efficiency of 98.9% is achieved at a higher current density of 10 mA g− 1. After the microporous carbon is charged and discharged at a lower current density of 7 mA g− 1 for 8 cycles, a capacity of 394 mAh g− 1 and a coulombic efficiency of 99.0% are achieved. Element analysis indicates that a certain amount of H and N exist in this microporous carbon.  相似文献   

20.
Current research on vanadium oxides in lithium ion batteries (LIBs) considers them as cathode materials, whereas they are rarely studied for use as anodes in LIBs because of their low electrical conductivity and rapid capacity fading. In this work, hydrogenated vanadium oxide nanoneedles were prepared and incorporated into freeze-dried graphene foam. The hydrogenated vanadium oxides show greatly improved charge-transfer kinetics, which lead to excellent electrochemical properties. When tested as anode materials (0.005–3.0 V vs. Li/Li+) in LIBs, the sample activated at 600 °C exhibits high specific capacity (~941 mA·h·g?1 at 100 mA·g?1) and high-rate capability (~504 mA·h·g?1 at 5 A·g?1), as well as excellent cycling performance (~285 mA·h·g?1 in the 1,000th cycle at 5 A·g?1). These results demonstrate the promising application of vanadium oxides as anodes in LIBs.
  相似文献   

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