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Yoo E  Kim J  Hosono E  Zhou HS  Kudo T  Honma I 《Nano letters》2008,8(8):2277-2282
The lithium storage properties of graphene nanosheet (GNS) materials as high capacity anode materials for rechargeable lithium secondary batteries (LIB) were investigated. Graphite is a practical anode material used for LIB, because of its capability for reversible lithium ion intercalation in the layered crystals, and the structural similarities of GNS to graphite may provide another type of intercalation anode compound. While the accommodation of lithium in these layered compounds is influenced by the layer spacing between the graphene nanosheets, control of the intergraphene sheet distance through interacting molecules such as carbon nanotubes (CNT) or fullerenes (C60) might be crucial for enhancement of the storage capacity. The specific capacity of GNS was found to be 540 mAh/g, which is much larger than that of graphite, and this was increased up to 730 mAh/g and 784 mAh/g, respectively, by the incorporation of macromolecules of CNT and C60 to the GNS.  相似文献   

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Li2.6Co0.4N anode material was prepared by solid-state reaction. The material was used to prepare Li2.6Co0.4N/natural graphite composite anode materials with the aim to improve the electrochemical performance of natural graphite. Natural graphite showed a low initial columbic efficiency of 69%, which was improved to ~ 100% by adding 20 wt.% of Li2.6Co0.4N into the material. On the other hand, the composite materials showed better capacity retention than both pure Li2.6Co0.4N and natural graphite. The material containing 20 wt.% of Li2.6Co0.4N exhibited a reversible discharge capacity of 243 mAh g? 1 after thirty cycles, as compared to a capacity of 212 mAh g? 1 for natural graphite.  相似文献   

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姚经文  吴锋 《功能材料》2006,37(11):1752-1754
采用高温固相反应法制备尖晶石相Li4Ti5O12负极材料.初步研究了反应温度和反应时间对Li4Ti5O12电化学性能的影响.XRD衍射未观测到TiO2残余存在;电化学测试显示,1.2~2.5V恒流充放电,其可逆容量达158.3mAh/g,首次库仑效率为95.2%;循环20周其容量衰减率仅为3.1%.  相似文献   

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The morphology and electronic structure of a Li4Ti5O12 anode are known to determine its electrical and electrochemical properties in lithium rechargeable batteries. Ag-Li4Ti5O12 nanofibers have been rationally designed and synthesized by an electrospinning technique to meet the requirements of one-dimensional (1D) morphology and superior electrical conductivity. Herein, we have found that the 1D Ag-Li4Ti5O12 nanofibers show enhanced specific capacity, rate capability, and cycling stability compared to bare Li4Ti5O12 nanofibers, due to the Ag nanoparticles (<5 nm), which are mainly distributed at interfaces between Li4Ti5O12 primary particles. This structural morphology gives rise to 20% higher rate capability than bare Li4Ti5O12 nanofibers by facilitating the charge transfer kinetics. Our findings provide an effective way to improve the electrochemical performance of Li4Ti5O12 anodes for lithium rechargeable batteries.   相似文献   

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Lithium(Li)metal with high theoretical capacity and low electrochemical potential is the most ideal anode for next-generation high-energy batteries.However,the practical implementation of Li anode has been hindered by dendritic growth and volume expansion during cycling,which results in low Coulombic efficiency(CE),short lifespan,and safety hazards.Here,we report a highly stable and dendrite-free Li metal anode by utilizing N-doped hollow porous bowl-like hard carbon/reduced graphene nanosheets(CB@rGO)hybrids as three-dimensional(3D)conductive and lithiophilic scaffold host.The lithiophilic carbon bowl(CB)mainly works as excellent guides during the Li plating process,whereas the rGO layer with high conductivity and mechanical stability maintains the integrity of the composite by confining the volume change in long-range order during cycling.Moreover,the local current density can be reduced due to the 3D conductive framework.Therefore,CB@rGO presents a low lithium metal nucleation overpotential of 18 mV,high CE of 98%,and stable cycling without obvious voltage fluctuation for over 600 cycles at a current density of 1 mA cm-2.Our study not only provides a good CB@rGO host and pre-Lithiated CB@rGO composite anode electrode,but also brings a new strategy of designing 3D electrodes for those active materials suffering from severe volume expansion.  相似文献   

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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   

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Owing to the present exponential development of portable consumer electronics and to the increasing concern about the environment, new energy sources are required that provide more energy in the same volume and/or mass. Within a short period of time, less than three years, many changes in the area of rechargeable batteries for the consumer market have occurred, along with the emergence of several new technologies. The ubiquitous Ni? Cd cells, which are environmentally unfriendly because of the toxicity of Cd, will be replaced by Ni-metal hydride, rocking-chair lithium (or Li-ion), and lithium polymer electrolyte rechargeable cells. This paper reviews recent advances in the field of Li-ion rechargeable batteries.  相似文献   

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Xue  Mingzhe  Lu  Wanzheng  Xue  Song  Zhang  Cunman 《Journal of Materials Science》2021,56(35):19614-19622

Garnet Li7La3Zr2O12 (LLZO) is a promising solid-state electrolyte (SSE) candidate for advanced solid-state lithium batteries (SSLBs). In this work, Li6.25La3Zr2-yAlxTayO12 (x?=?0.25, y?=?0; x?=?0.2, y?=?0.15; x?=?0.15, y?=?0.3; x?=?0.1, y?=?0.45; x?=?0.05, y?=?0.6) and Li6.4La3Zr1.4Ta0.6O12 (LLZT0.6O) ceramic electrolytes, are prepared via a simple sol–gel process. The effect of Al and Ta co-doping levels on the phase, the microstructure and the ionic conductivity of modified LLZO is discussed in detail. Those Al/Ta co-doped LLZO ceramics (LLZATO) with Ta?≥?0.3 per formula unit, are nearly pure cubic structures with a trace of new phases. The ionic conductivities of Li6.25La3Zr1.55Al0.1Ta0.45O12 (LLZA0.1T0.45O) and Li6.25La3Zr1.4Al0.05Ta0.6O12 (LLZA0.05T0.6O), are greatly improved by co-doping Al and Ta, benefitting from the emergence of self-grown LiAlO2 phase, and the microstructure of large grains contacting small grains. Remarkably, the optimal LLZA0.1T0.45O delivers a high ionic conductivity of 6.70?×?10–4 S cm?1 and a low electronic conductivity?~?9.83?×?10–8 S cm?1 at 25 °C. This work provides available enhanced Al/Ta co-doped LLZO ceramic electrolytes with the reduced Ta doping level for solid-state lithium batteries.

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Rechargeable lithium batteries are attractive power sources for electronic devices and are being aggressively developed for vehicular use. Nevertheless, problems with their safety and reliability must be solved for the large-scale use of lithium batteries in transportation and grid-storage applications. In this study, a unique hybrid solid-state electrolyte composed of an ionic liquid electrolyte (LiTFSI/Pyr14TFSI) and BaTiO3 nanosize ceramic particles was prepared without a polymer. The electrolyte exhibited high thermal stability, a wide electrochemical window, good ionic conductivity of 1.3 × 10?3 S·cm?1 at 30 °C, and a remarkably high lithium-ion transference number of 0.35. The solid-state LiFePO4 cell exhibited the best electrochemical properties among the reported solid-state batteries, along with a reasonable rate capability. Li/LiCoO2 cells prepared using this nanocomposite solid electrolyte exhibited high performance at both room temperature and a high temperature, confirming their potential as lithium batteries with enhanced safety and a wide range of operating temperatures.
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锂离子二次电池负极材料的研究综述   总被引:1,自引:0,他引:1  
总结了在碳材料、合金材料和复合材料等3个锂离子电池负极材料研发的主导方向上的开发情况和它们各自特点,描述了目前的研究所面临难题,给出了锂离子电池负极材料研发取得重大突破的可能途径和建议.  相似文献   

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A material flow of lithium batteries in Taiwan   总被引:1,自引:0,他引:1  
Li batteries, including secondary and cylindrical/button primary Li batteries, are used worldwide in computers, communications and consumer electronics products. However, there are several dangerous issues that occur during the manufacture, shipping, and storage of Li batteries. This study analyzes the material flow of lithium batteries and their valuable heavy metals in Taiwan for the year 2006 by material flow analysis. According to data from the Taiwan Environmental Protection Administration, Taiwan External Trade Development Council, Bureau of Foreign Trade, Directorate General of Customs, and the Li batteries manufactures/importers/exporters. It was found that 2,952,696 kg of Li batteries was input into Taiwan for the year 2006, including 2,256,501 kg of imported Li batteries and 696,195 kg of stock Li batteries in 2005. In addition, 1,113,867 and 572,215 kg of Li batteries was domestically produced and sold abroad, revealing that 3,494,348 kg of different types of Li batteries was sold in Taiwan. Of these domestically sold batteries, 504,663 and 146,557 kg were treated domestically and abroad. Thus, a total of 2,843,128 kg of Li batteries was stored by individual/industry users or illegally disposed. In addition, it was also observed that 2,120,682 kg of heavy metals contained in Li batteries, including Ni, Co, Al, Cu and Ni, was accumulated in Taiwan, with a recycled value of 38.8 million USD. These results suggest that these heavy metals should be recovered by suitable collection, recycling and reuse procedures.  相似文献   

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A novel microwave method is described for the preparation of electrode materials required for lithium batteries. The method is simple, fast and carried out in most cases with the same starting material as in conventional methods. Good crystallinity has been noted and lower temperatures of reaction has been inferred in cases where low temperature products have been identified  相似文献   

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Wang  Chunhua  Bai  Guoliang  Yang  Yifu  Liu  Xingjiang  Shao  Huixia 《Nano Research》2019,12(1):217-223
Nano Research - Dendrite formation on lithium (Li) metal anode is a key issue which hinders the development of rechargeable Li battery seriously. A novel method for suppressing Li dendrites via...  相似文献   

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锂离子电池内阻测试方法研究   总被引:1,自引:0,他引:1  
在深入研究锂离子电池内阻形成原理的基础上,通过对现有锂离子电池内阻测试方法的分析研究,证明了利用锁相放大器提高交流内阻测量精度的原理方法,并提出了基于不同荷电状态下的直流内阻谱概念和不同频率下的交流内阻谱概念.由于内阻谱包含了更多电池性能方面的信息,在实际测量中与传统测量方法相比有一定的优越性.  相似文献   

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