共查询到20条相似文献，搜索用时 62 毫秒
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动力电池领域对锂二次电池的能量密度和安全性提出了更高要求,研究高能量密度固态锂电池对发展新能源产业具有重要意义。相比传统的有机电解液锂离子电池,采用聚合物固体电解质的聚合物固态锂电池不但具有明显提升的安全性,而且能够匹配高容量电极材料,实现能量密度的有效提升。聚合物固态锂电池是最有前景的锂二次电池之一,然而聚合物固体电解质与锂负极间仍存在严重的界面副反应、锂负极表面易生长枝晶等问题。近年来,通过电解质成分调控、电解质力学性能提升、电解质/锂负极界面调控和匹配三维锂负极等手段,聚合物基固态锂电池性能明显提升。基于此,本文介绍了常见的聚合物固体电解质及其与锂负极间的界面挑战,从添加无机填料、使用高强度基底膜、分级层状结构设计、构筑界面缓冲层、交联网络设计以及固态锂负极保护等几个方面综述了提升聚合物基电解质/锂负极界面稳定性的最新研究成果,最后对解决聚合物固体电解质/锂负极界面兼容性的研发方向和发展趋势进行了展望。 相似文献
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本文通过在锂负极中熔入少量铝制备了一种含Al-Li合金(Al4Li9)的新型复合锂负极,可有效改善Garnet/金属锂界面润湿性,从而显著降低了界面阻抗.XRD研究结果表明这一复合锂负极由Al4Li9合金和金属锂两相复合而成.SEM研究表明,复合锂负极可以有效改善金属锂与Garnet电解质的界面接触,形成更为紧密的接触界面.电化学测试表明,复合锂负极显著降低了金属锂与Garnet电解质的界面阻抗,界面阻抗由锂/Garnet电解质界面的740.6Ω·cm^2降低到复合锂负极/Garnet电解质界面的75.0Ω·cm^2.使用复合锂负极制备的对称电池在50μA·cm^-2和100μA·cm^-2电流密度锂沉积-溶出过程中表现出较低的极化和良好的循环稳定性,在50μA·cm^-2电流密度下,可以稳定循环超过400小时. 相似文献
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复合型聚合物电解质的研究进展 总被引：5，自引：1，他引：5
综述了通过物理改性的方法制成的复合型聚合物电解质（ＣＰＥ）的研究进展,并介绍了ＣＰＥ薄膜的制备工艺,以及ＣＰＥ应用在聚合物二次锂电池中的最新成果。 相似文献
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锂电池目前在人们生活中已经得到广泛应用,但是传统的液体电解质沸点低且易泄漏,容易引起锂枝晶生长和安全问题。凝胶聚合物电解质(GPEs)的状态介于液态电解质和固态电解质之间,不仅可以作为电解质,还可以作为隔膜,这样可以减少液体电解质的泄漏以及改善固体电解质的界面电阻。本文综述了锂电池中制备不同类型的GPEs的方法,如溶液浇铸法、相转化法、原位聚合法、UV(紫外)固化法和静电纺丝法等,重点总结了不同纤维基的GPEs(聚(偏二氟乙烯)(PVDF)、聚(偏二氟乙烯-共六氟丙烯)(PVDF- HFP)、聚甲基丙烯酸甲酯(PMMA)、聚丙烯腈(PAN)和聚间亚苯基间苯二甲酰胺(PMIA))在锂电池中的运用,并通过对不同基质的改性来改善电解质的离子电导率,阻碍锂枝晶的生长。最后,本文对锂电池中GPEs的未来发展前景进行了展望,讨论和提出的策略将为今后高性能锂电池的实际应用提供更多的途径。 相似文献
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聚合物电解质界面性质交流阻抗研究 总被引：2，自引：0，他引：2
合成了一种新型聚合物基质材料聚(甲基丙烯酸甲酯-丙烯腈-甲基丙烯酸锂)(简记为PMAML),并以PMAML/PVDF-HFP(偏氟乙烯-六氟丙烯共聚合物)复合物为基质制备了聚合物电解质.利用FTIR对合成的PMAML进行结构表征,并用扫描电镜观察聚合物基质膜的表面形貌.聚合物电解质由聚合物基质膜浸渍电解质溶液得到,其室温电导率可达到2.6×10－3 S• cm－1.利用交流阻抗技术研究了聚合物电解质与锂电极间的界面性质,并考察了开路放置时间、循环伏安及恒流充电对界面阻抗的影响.结果表明,聚合物电解质与锂电极界面阻抗随放置时间的延长而增加,更新锂电极表面可降低界面阻抗,PMAML能提高界面稳定性. 相似文献
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Scrosati B 《Chemical record (New York, N.Y.)》2001,1(2):173-181
The electrochemical and physical-chemical properties of two families of lithium ion conducting membranes, i.e., the blends between high molecular weight poly(ethylene oxide) with a lithium salt commonly named \"polymer electrolytes\" and the gels of liquid solutions in a polymer matrix commonly named \"gel electrolytes,\" are repoted and discussed. Particular attention is devoted to the newly developed approach of dispersing ceramic powders at the nanoscale particle dimension into the two types of membranes. This leads \"nanocomposite\" membranes having unique features, such as improved transport and interfacial properties in the case of the polymer electrolytes and enhanced liquid retention capability in the case of the gel electrolytes. Finally, the use of the gel electrolytes for the development of new-design, plastic-like, lithium-ion batteries is illustrated. 相似文献
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Boram Kim Haneol Kang Kyoungwook Kim Dr. Rui-Yang Wang Prof. Moon Jeong Park 《ChemSusChem》2020,13(9):2271-2279
Advances in lithium battery technologies necessitate improved energy densities, long cycle lives, fast charging, safe operation, and environmentally friendly components. This study concerns lithium–organic batteries comprising bioinspired poly(4-vinyl catechol) (P4VC) cathode materials and single-ion conducting polymer nanoparticle electrolytes. The controlled synthesis of P4VC results in a two-step redox reaction with voltage plateaus at around 3.1 and 3.5 V, as well as a high initial specific capacity of 352 mAh g−1. The use of single-ion nanoparticle electrolytes enables high electrochemical stabilities up to 5.5 V, a high lithium transference number of 0.99, high ionic conductivities, ranging from 0.2×10−3 to 10−3 S cm−1, and stable storage moduli of >10 MPa at 25–90 °C. Lithium cells can deliver 165 mAh g−1 at 39.7 mA g−1 for 100 cycles and stable specific capacities of >100 mAh g−1 at a high current density of 794 mA g−1 for 500 cycles. As the first successful demonstration of solid-state single-ion polymer electrolytes in environmentally benign and cost-effective lithium–organic batteries, this work establishes a future research avenue for advancing lithium battery technologies. 相似文献
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A variety of disubstituted (double-comb) polysiloxane polymers have been prepared containing linear, branched, and cyclic oligoethyleneoxide units, –(OCH2CH2)n–, in the side chains and as part of the siloxane backbone. Copolymers, using mixtures of linear ethylene oxide side chains, were also synthesized. These polymers were doped with LiN(SO2CF3)2 (LiTFSI, 1) and conductivities of the polymer-salt complexes were determined as a function of temperature and doping level. The maximum conductivity of these polymers at 25 ° C was 2.99 ×10–4, for a copolymer containing equimolar amounts of side chains with n = 5 and 6. 相似文献
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Boram Kim Haneol Kang Kyoungwook Kim Dr. Rui-Yang Wang Prof. Moon Jeong Park 《ChemSusChem》2020,13(9):2104-2104
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The formation of a robust solid-electrolyte interphase (SEI) layer at the surface of a graphite anode by electrolyte control is a key technology for high-performance lithium-ion batteries. Although propylene carbonate (PC) offers a lower melting point than ethylene carbonate, its combination with the graphite anode without additive is a worse choice, owing to co-intercalation of PC and Li+ ion into graphite, exfoliation of graphene sheets, and death of the battery. This study reports a graphite anode with an unprecedentedly high initial coulombic efficiency of 94 %, close to theoretical capacity, and excellent capacity retention of 99 % after 100 cycles in a PC-based electrolyte system, even at an unusually high rate of 0.2 C, which is generally attainable only at a very low rate of below 0.05 C in commercial electrolyte. The SEI stabilization for a graphite anode in PC-based electrolyte provides a new avenue for high-energy and high-performance batteries in widened range of working temperatures. A strong correlation between anode-electrolyte interfacial stabilization and highly reversible cycling performance is clearly demonstrated. 相似文献
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Lukas Stolz Dr. Gerrit Homann Prof. Martin Winter Dr. Johannes Kasnatscheew 《ChemSusChem》2021,14(10):2163-2169
Systematic and systemic research and development of solid electrolytes for lithium batteries requires a reliable and reproducible benchmark cell system. Therefore, factors relevant for performance, such as temperature, voltage operation range, or specific current, should be defined and reported. However, performance can also be sensitive to apparently inconspicuous and overlooked factors, such as area oversizing of the lithium electrode and the solid electrolyte membrane (relative to the cathode area). In this study, area oversizing is found to diminish polarization and improves the performance in LiNi0.6Mn0.2Co0.2O2 (NMC622)||Li cells, with a more pronounced effect under kinetically harsh conditions (e. g., low temperature and/or high current density). For validity reasons, the polarization behavior is also investigated in Li||Li symmetric cells. Given the mathematical conformity of the characteristic overvoltage behavior with the Sand's equation, the beneficial effect is attributed to lower depletion of Li ions at the electrode/electrolyte interface. In this regard, the highest possible effect of area oversizing on the performance is discussed, that is when the accompanied decrease in current density and overvoltage overcomes the Sand's threshold limit. This scenario entirely prevents the capacity decay attributable to Li+ depletion and is in line with the mathematically predicted values. 相似文献
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Lukas Stolz Dr. Gerrit Homann Prof. Martin Winter Dr. Johannes Kasnatscheew 《ChemSusChem》2021,14(10):2141-2141
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Qiang Ma Heng Zhang Chongwang Zhou Liping Zheng Pengfei Cheng Prof. Jin Nie Prof. Wenfang Feng Prof. Yong‐Sheng Hu Prof. Hong Li Prof. Xuejie Huang Prof. Liquan Chen Prof. Michel Armand Prof. Zhibin Zhou 《Angewandte Chemie (International ed. in English)》2016,55(7):2521-2525
A novel single lithium‐ion (Li‐ion) conducting polymer electrolyte is presented that is composed of the lithium salt of a polyanion, poly[(4‐styrenesulfonyl)(trifluoromethyl(S‐trifluoromethylsulfonylimino)sulfonyl)imide] (PSsTFSI?), and high‐molecular‐weight poly(ethylene oxide) (PEO). The neat LiPSsTFSI ionomer displays a low glass‐transition temperature (44.3 °C; that is, strongly plasticizing effect). The complex of LiPSsTFSI/PEO exhibits a high Li‐ion transference number (tLi+=0.91) and is thermally stable up to 300 °C. Meanwhile, it exhibits a Li‐ion conductivity as high as 1.35×10?4 S cm?1 at 90 °C, which is comparable to that for the classic ambipolar LiTFSI/PEO SPEs at the same temperature. These outstanding properties of the LiPSsTFSI/PEO blended polymer electrolyte would make it promising as solid polymer electrolytes for Li batteries. 相似文献
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Jirong Wang Chi Zhang Yong Zhang Zhigang Xue 《Journal of polymer science. Part A, Polymer chemistry》2022,60(5):743-765
Polymer electrolyte (PE) has been emerging as a promising alternative to liquid electrolytes due to the unique advantages such as excellent flexibility and processability, high chemical and thermal stability, and low risk of leakage and combustion, especially for lithium-ion batteries (LIBs). Even though abundant attempts focusing on polymer chemistries have been made, the inadequate capacity of lithium-ion transport via segmental motion still cannot provide satisfying room temperature ionic conductivity and lithium-ion transference number. In addition, safety concerns and short lifespan resulted from the brittle and incompatible interface between the electrode and polymer materials also hinder the commercialization of PEs-based LIBs. Hence, for the above performance defects and interface issues, this review provides an overview of polymer electrolytes from the conductivity improvement, polymer selection and mechanical strength enhancement for protrusion suppressing. The improvement of conductivity specifically includes structure modification of poly(ethylene oxide) (PEO) host and novel electrolyte matrix beyond PEO, while the section of interface regulation mainly involves dendrite-inhibited polymers, mechanical strengthening, and in situ polymerization. Finally, perspectives and challenges are pointed out in the development of polymer electrolytes with both excellent electrochemical performance and safety for LIBs. 相似文献