共查询到19条相似文献,搜索用时 125 毫秒
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双乙二酸硼酸锂(LiBOB)被认为是一种很有潜力代替LiPF6应用在锂离子电池中的新型电解质锂盐,它不仅满足了电解质对锂盐的基本要求,而且具有良好的成膜性能和热稳定性,是近年来受到人们广泛关注的新型锂盐之一。 相似文献
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锂离子电池非水电解质锂盐的研究进展 总被引:5,自引:1,他引:4
新型电解质锂盐主要包括含螯合硼阴离子、螯合磷阴离子、全氟膦阴离子、烷基磺酸阴离子、全氟烷基、亚胺基的有机锂盐及有机铝酸锂盐.本文综述了近年来在新型电解质锂盐研究与探索方面的成果,介绍了锂离子电池电解质锂盐的合成方法、组成与结构、化学和电化学性能及其与结构的关系,并阐述今后电解质锂盐研究的可能发展方向及研究方法. 相似文献
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锂离子电池有机电解液材料研究进展 总被引:4,自引:0,他引:4
综述了锂离子电池有机电解液材料的研究现状。锂离子电池有机电解液主要由电解质锂盐、有机溶剂和添加剂三个部分组成,新型电解质锂盐的研究开发可分为三个方面:(1)LiTFSI及其类似物;(2)络合硼酸锂化合物;(3)络合磷酸锂化合物。有机溶剂的研究工作主要集中在新型有机溶剂的开发上。最重要的添加剂主要有三类:(1)主要用以改善碳负极SEI膜性能的添加剂;(2)过充电保护添加剂;(3)配体添加剂。 相似文献
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Aravindan V Gnanaraj J Madhavi S Liu HK 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(51):14326-14346
This paper presents an overview of the various types of lithium salts used to conduct Li(+) ions in electrolyte solutions for lithium rechargeable batteries. More emphasis is paid towards lithium salts and their ionic conductivity in conventional solutions, solid-electrolyte interface (SEI) formation towards carbonaceous anodes and the effect of anions on the aluminium current collector. The physicochemical and functional parameters relevant to electrochemical properties, that is, electrochemical stabilities, are also presented. The new types of lithium salts, such as the bis(oxalato)borate (LiBOB), oxalyldifluoroborate (LiODFB) and fluoroalkylphosphate (LiFAP), are described in detail with their appropriate synthesis procedures, possible decomposition mechanism for SEI formation and prospect of using them in future generation lithium-ion batteries. Finally, the state-of-the-art of the system is given and some interesting strategies for the future developments are illustrated. 相似文献
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用于锂离子电池聚合物电解质的组成、结构和性能 总被引:1,自引:0,他引:1
聚合物电解质是全固态锂离子电池的重要组成部分, 其电导率对电池的性能有很重要的影响.本文综述了聚合物电解质的组成、结构和性能对锂 离子电池导电率影响的最新研究进展,特别是介绍了聚合物-碱金属盐复合电解质和聚离子体电解质两个体系的研究进展. 相似文献
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S. Y. Li X. L. Cui X. L. Xu X. M. Shi G. X. Li 《Russian Journal of Electrochemistry》2012,48(5):518-524
Conductivities (??) of PC (propylene carbonate)/EMC (ethyl methyl carbon ate)/DMC (dimethyl carbonate) and EC (ethylene carbonate)/EMC/DMC solutions of lithium bis(oxalate)borate (LiBOB) were experimentally determined at a temperature (??) range from ?40.0 to 60.0°C. Under such experimental conditions, the effect factors on the ??, such as the salt molar concentrations (m), and the volume ratio of solvent compositions, were also investigated. The results showed that, in wide ?? range, the higher ?? were obtained with 0.7 mol L?1 LiBOB in PC/EMC/DMC and 0.6 mol L?1 LiBOB in EC/EMC/DMC and with a volume ratio of 1: 1: 1 and 1: 1: 2, respectively. When used in LiFePO4/Li cells, compared to the cell with the electrolyte system of 1.0 mol L?1 LiPF6-EC/EMC/DMC (1: 1: 1), LiBOB cells with PC/EMC/DMC and EC/EMC/DMC electrolyte systems with the same volume mixture solvent compositions exhibit several advantages, such as more stable cycle performance, higher mean voltage, excellent large current discharge capability, more capacity retention at high temperature, and more stable storage performance, etc. This study not only shows that LiBOB is a very promising alternative salt for lithium ion chemistry, but also provides appropriate solvent to improve LiBOB??s electrochemical performance. 相似文献
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Tao Yu Jinliang Liu Hongming Zhang Shiyou Li Xiaoling Cui Huixia Feng Yangyu Zhao Haining Liu Faqiang Li 《Surface and interface analysis : SIA》2014,46(1):48-55
To discuss the source of sulfolane (SL) in decreasing the interface resistance of Li/mesophase carbon microbeads cell with lithium bis(oxalate)borate (LiBOB)‐based electrolyte, the morphology and the composition of the solid electrolyte interphase (SEI) layer on the surface of carbonaceous anode material have been investigated. Compared with the cell with 0.7 mol l?1 LiBOB‐ethylene carbonate/ethyl methyl carbonate (EMC) (1 : 1, v/v) electrolyte, the cell with 0.7 mol l?1 LiBOB‐SL/EMC (1 : 1, v/v) electrolyte shows better film‐forming characteristics in SEM (SEI) spectra. According to the results obtained from Fourier transform infrared spectroscopy, XPS, and density functional theory calculations, SL is reduced to Li2SO3 and LiO2S(CH2)8SO2Li through electrochemical processes, which happens prior to the reduction of either ethylene carbonate or EMC. It is believed that the root of impedance reduction benefits from the rich existence of sulfurous compounds in SEI layer, which are better conductors of Li+ ions than analogical carbonates. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
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锂金属电池作为下一代高比能量电池技术受到人们越来越广泛的关注。然而由锂枝晶生长引发的安全问题是锂金属电池商业化面临的最大挑战之一。具有高锂离子迁移数和离子电导率的聚合物电解质是抑制锂枝晶生长的重要策略之一。本文将季戊四醇四丙烯酸酯和自由基引发剂AIBN添加至商业化电解液中,采用具有单离子传导功能的多孔聚合物电解质为锂金属电池的电解质隔膜,通过在电池内部发生热诱导原位聚合制备三维半互穿网络单离子传导聚合物电解质,达到提高电解质隔膜离子电导率和机械拉伸性能,以及有效抑制锂枝晶生长的目的。通过该策略的实施,成功获得了室温离子电导率0.53 mS·cm-1和锂离子迁移数0.65的良好结果。应用于锂金属电池,证明该电解质能够有效抑制锂枝晶的生长和倍率性能的提高,为锂金属电池的开发提供了良好的解决路径。 相似文献
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Solid‐State Electrolyte Anchored with a Carboxylated Azo Compound for All‐Solid‐State Lithium Batteries 下载免费PDF全文
Dr. Chao Luo Xiao Ji Dr. Ji Chen Dr. Karen J. Gaskell Xinzi He Dr. Yujia Liang Prof. Jianjun Jiang Prof. Chunsheng Wang 《Angewandte Chemie (International ed. in English)》2018,57(28):8567-8571
Organic electrode materials are promising for green and sustainable lithium‐ion batteries. However, the high solubility of organic materials in the liquid electrolyte results in the shuttle reaction and fast capacity decay. Herein, azo compounds are firstly applied in all‐solid‐state lithium batteries (ASSLB) to suppress the dissolution challenge. Due to the high compatibility of azobenzene (AB) based compounds to Li3PS4 (LPS) solid electrolyte, the LPS solid electrolyte is used to prevent the dissolution and shuttle reaction of AB. To maintain the low interface resistance during the large volume change upon cycling, a carboxylate group is added into AB to provide 4‐(phenylazo) benzoic acid lithium salt (PBALS), which could bond with LPS solid electrolyte via the ionic bonding between oxygen in PBALS and lithium ion in LPS. The ionic bonding between the active material and solid electrolyte stabilizes the contact interface and enables the stable cycle life of PBALS in ASSLB. 相似文献
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将聚乙二醇单甲醚(MPEG)接枝在聚(异丁烯-alt-马来酸酐)(PIAMA)上合成梳状锂单离子导体PIAMA-g-MPEG, 并与双(三氟甲基磺酰)亚胺锂(LiTFSI)复合制成双锂盐梳状聚合物电解质薄膜. 用核磁共振波谱 (1H NMR)、 热重分析(TG)、 扫描电子显微镜(SEM)、 电化学阻抗(EIS)和电池充放电测试等方法对聚合物基体和电解质的物化性质和电化学性能进行了研究.结果表明, 设计的双锂盐梳状聚合物电解质能够有效解离并传输锂离子, 70 ℃下离子迁移数(tLi+)为0.32, 离子电导率(σ)为1.5×10-4 S/cm, 电化学稳定窗口为0~4.9 V (vs. Li/Li+). 组装Li|PIAMA-g-MPEG|Li电池并进行70 ℃恒电流充放电电压极化测试, 结果表明, 电解质与金属锂负极兼容性较好, 能够有效抑制锂枝晶的生长.组装LiFePO4|PIAMA-g-MPEG|Li电池进行70 ℃长循环及倍率性能测试, 电解质表现出了优异的高温性能. 相似文献
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Yaduo Song Yanxin Jiang Prof. Longjiang Deng Prof. Guang Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(72):e202202717
Developing high-performance functional polymer-based electrolytes is important for realizing next generation safe lithium metal batteries. In this study, a new type of quasi-solid polymer network electrolyte (SIPH-x-y%) was prepared by combining synthesized polymer network (SIPH) containing urethane bond linked ionic liquids (ILs), polyethylene glycol (PEG), and disulfide bond moieties, lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI), and glyme type additive. It was found that SIPH-20-40% was mechanically flexible, self-healable, and showed high ionic conductivity of 2.67×10−4 S cm−1. Also, SIPH-20-40% possesses a high lithium ion transference number of 0.43 and good electrochemical stability. These properties enabled the SIPH-20-40% electrolyte membrane to support Li/Li symmetrical cell to cycle stably during long term Li plating and stripping. The Li/SIPH-20-40%/LFP showed high delivered specific capacity and good stability (166.1 mAh g−1 after 106 cycles at 0.2 C). Such glyme doped polymer network electrolyte provides new experimental findings for developing polymer-based electrolyte with excellent mechanical integrity and battery related properties. 相似文献