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181.
Monika Osińska Mariusz Walkowiak Aldona Zalewska Teofil Jesionowski 《Journal of membrane science》2009
The presented contribution aims at reconsidering the role of filler in affecting the ionic transport in composite gel electrolytes for Li-ion cells based on microporous polymer membranes. The gels have been prepared by swelling thin PVdF/HFP membranes either with conventional liquid electrolyte or with pure propylene carbonate solvent. The membranes contained dispersed submicron-size modified silica filler added in a wide range of weight ratios. The effect of filler content on the kinetics of liquid phase absorption and evaporation from the composite membranes, as well as on the conductivity of the corresponding gel electrolytes, has been studied and discussed in terms of the “colloidal” and “soggy sand” electrolyte concepts. It has been found that conductivity increase of composite gels is not directly correlated with the liquid electrolyte uptake. On this basis it is concluded that important part of ionic transport in this type of composite gel polymer electrolytes is realized on the filler grain boundaries, through overlapping space charge layers of the silica grains. 相似文献
182.
低成本、高性能的钠离子电池有望成为代替锂离子电池的下一代核心器件.但是开发出高比容量、高倍率的钠离子电池负极材料依然是瓶颈.本文通过水热/溶剂热法制备了Co基前驱体,然后将其一步硫/磷热处理制得具有空心多孔结构的h-Co9S8/CoP/C纳米复合材料.通过X-射线粉末衍射(XRD)、拉曼光谱(Raman)、扫描电镜(SEM)、透射电镜(TEM)和X-射线光电子能谱(XPS)等表征以确定纳米复合物的物相以及形貌特征.当h-Co9S8/CoP/C作为钠离子电池负极材料时,该电极材料展示了高的比容量(561 mAh g-1@0.1 Ag-1)、较好的循环性能(可逆比容量200 mAh g-1@2 Ag-1)和倍率性能.h-Co9S8/CoP/C之所以显示出良好的储钠性能,主要得益于其空心多孔结构不仅提供更多的空间缓解钠在反复嵌入和脱出过程造成的体积膨胀效应,而且可以缩短离子/电荷扩散途径以加快反应动力学,此外,Co9S8、CoP和C独特的电子结构优势得以共同发挥. 相似文献
183.
《Journal of Energy Chemistry》2014,23(2):207-212
Ultrathin MoS2nanosheets were prepared in high yield using a facile and effective hydrothermal intercalation and exfoliation route. The products were characterized in detail using X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. The results show that the high yield of MoS2nanosheets with good quality was successfully achieved and the dimensions of the immense nanosheets reached 1 μm–2 μm. As anode material for Li-ion batteries, the as-prepared MoS2nanosheets electrodes exhibited a good initial capacity of 1190 mAh g-1and excellent cyclic stability at constant current density of 50 mA g-1. After 50 cycles, it still delivered reversibly sustained high capacities of 750 mAh g-1. 相似文献
184.
Synthesis of Highly Uniform Molybdenum–Glycerate Spheres and Their Conversion into Hierarchical MoS2 Hollow Nanospheres for Lithium‐Ion Batteries 下载免费PDF全文
Dr. Yawen Wang Dr. Le Yu Prof. Xiong Wen Lou 《Angewandte Chemie (International ed. in English)》2016,55(26):7423-7426
Highly uniform Mo–glycerate solid spheres are synthesized for the first time through a solvothermal process. The size of these Mo–glycerate spheres can be easily controlled in the range of 400–1000 nm by varying the water content in the mixed solvent. As a precursor, these Mo–glycerate solid spheres can be converted into hierarchical MoS2 hollow nanospheres through a subsequent sulfidation reaction. Owing to the unique ultrathin subunits and hollow interior, the as‐prepared MoS2 hollow nanospheres exhibit appealing performance as the anode material for lithium‐ion batteries. Impressively, these hierarchical structures deliver a high capacity of about 1100 mAh g?1 at 0.5 A g?1 with good rate retention and long cycle life. 相似文献
185.
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
186.
In this work, P2-Na0.6[Mg(II)0.3Mn(IV)0.7] O2 with inoxidizable elements (Na+, Mg2+ and Mn4+) except O2- was synthesized and investigated, which exhibited high reversible capacity (~210 mAh/g) with highly reversible ARR characteristic. 相似文献
187.
M. Sc. Shih‐Fan Hsu Dipl.‐Chem. Susanne Rommel M. Sc. Philipp Eversfield Dr. Keven Muller Prof. Dr. Elias Klemm Prof. Dr. Werner R. Thiel Prof. Dr. Bernd Plietker 《Angewandte Chemie (International ed. in English)》2014,53(27):7074-7078
Apart from energy generation, the storage and liberation of energy are among the major problems in establishing a sustainable energy supply chain. Herein we report the development of a rechargeable H2 battery which is based on the principle of the Ru‐catalyzed hydrogenation of CO2 to formic acid (charging process) and the Ru‐catalyzed decomposition of formic acid to CO2 and H2 (discharging process). Both processes are driven by the same catalyst at elevated temperature either under pressure (charging process) or pressure‐free conditions (discharging process). Up to five charging–discharging cycles were performed without decrease of storage capacity. The resulting CO2/H2 mixture is free of CO and can be employed directly in fuel‐cell technology. 相似文献
188.
贮氢合金材料电化学与表面性能的研究进展①杨勇李骏林祖赓(厦门大学化学系,固体表面物理化学国家重点实验室,厦门361005)八十年代后期以来,人们对地球的环境保护提出了更高的要求,而便携式电器(如移动电话,摄像机与笔记本电脑等)对电池的需求也大量增加... 相似文献
189.
采用基于密度泛函理论的第一性原理方法, 计算了不同Mn掺杂浓度LiFe1-xMnxPO4 (x=0,0.25,0.50,0.75) 的电子结构. 同时采用流变相辅助高温固相碳热还原法制备了LiFe1-xMnxPO4 (x= 0,0.25,0.50,0.75) 材料. 理论计算表明: LiFePO4具有Eg = 0.725 eV的带隙宽度, 为半导体材料. 通过Fe位掺杂25%的Mn离子可最大程度地 减小材料带隙宽度、降低Fe---O键及Li---O键键能, 进而提高材料的电子电导率及锂离子扩散速率. 实验结果亦表明, 当Mn掺杂量x=0.25时, 材料具有最优的电化学性能, 其具有约为158 mAh· g-1的放电比容量以及551 Wh· kg-1的能量密度. 理论计算与实验结果非常符合. 相似文献
190.
石蕊溶液在碱性溶液中变色不明显,这个问题虽小,但它一直困扰着我们的实验教学活动。利用手机软件颜色识别器、数字传感器等几种软硬件技术手段,对石蕊试剂的选择、配制方法的优化、溶液pH的调节等方面进行探究,试图配制出在酸碱性溶液中显色明显的石蕊溶液。 相似文献