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排序方式: 共有4519条查询结果,搜索用时 15 毫秒
41.
Mun-Soo Yun Ki-Young Jeong Eui-Wan Lee Bong-Soo Jin Seong-In Moon Chil-Hoon Doh 《Korean Journal of Chemical Engineering》2006,23(2):230-236
The aim of this paper is to study the electrochemical behavior of Si-C material synthesized by heating a mixture of silicon
and polyvinylidene fluoride (PVDF) in the ratios of 5, 20, and 50 wt%. The particle size of the synthesized material was found
to be increased with increase in the PVDF ratio. The coexistence of silicon with carbon was confirmed from the XRD analysis.
A field emission scanning electron microscope (FESEM) study performed with the material proved the improvement in coating
efficiency with increase in the PVDF ratio. Coin cells of the type 2025 were made by using the synthesized material, and the
electrochemical properties were studied. An electrode was prepared by using the developed Si-C material. Si-C|Li cells were
made with this electrode. A charge|discharge test was performed for 20 cycles at 0.1 C hour rate. Initial charge and discharge
capacities of Si-C material derived from 20 wt% of PVDF was found to be 1,830 and 526 mAh|g, respectively. Initial charge/discharge
characteristics of the electrode were analyzed. The level of reversible specific capacity was about 216mAh/g at Si-C material
derived from 20 wt% of PVDF, initial intercalation efficiency (IIE), intercalation efficiency at initial charge/discharge,
was 68%. Surface irreversible specific capacity was 31 mAh/g, and average specific resistance was 2.6 ohm * g. 相似文献
42.
Ultrafine lithium ion conducting La2/3−xLi3xTiO3 (x = 0.11, LLT) powder was synthesized by a simple polymerizable complex method based on the Pechini-type process. The formation mechanism, homogeneity and microstructure of the samples were investigated by thermal analysis (TG/DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). XRD analysis indicated the formation of pure perovskite-type phase. The powder synthesized at a temperature as low as 900 °C in a much shorter time than solid-state reaction method was well crystallized. The lithium ion conductivity of the LLT ceramics sintered at 1200 °C was found to be 9 × 10−4 S/cm at room temperature. 相似文献
43.
Hajime Arai Masayuki Tsuda Masahiko Hayashi Hideaki Ohtsuka Yoji Sakurai 《Electrochimica acta》2005,50(9):1821-1828
Several polymorphs of layered nickel dioxide were prepared by using the chemical insertion of alkaline ions into Li0.10NiO2. We used aqueous AOH (A = Li, Na, K) solutions as reducing agents. Sodium and potassium insertion resulted in hydrated layered compounds that can be classified as γ-NiOOH with high crystallinity, while lithium insertion occurred without hydration. We discuss the coordination environment around the A+ ions for these inserted compounds. The thermal behavior, analyzed using high temperature (HT) X-ray diffraction (XRD) and thermogravimetric (TG) measurements, indicated that heating the hydrate at 150 °C yielded its dehydrate. The electrode performance of the nickelate was studied in lithium cells. We discuss the effect of interlayer water on cell rechargeability and the similarity between these nickelate and hydrated manganese dioxide (birnessite). 相似文献
44.
45.
Composite polymer electrolyte based on a new class of filler added to a PEGDME/LiClO4 model system has been investigated. “Ceramic super acids” used consist of grafted SO42− groups on Al2O3 particles surface obtained by calcinations route. Conductivity, DSC and FT-IR measurements performed on such composite electrolytes, when compared to the model PEGDME/LiClO4 electrolyte, showed only slight improvement of their inner characteristics. In contrary, Li/Li symmetric cells study, by means of impedance spectroscopy, has presented a spectacular decrease of the interfacial resistance compare to the model electrolyte. This result opens a new pathway of investigation to master the lithium metal/polymer electrolyte interface. 相似文献
46.
Polyelectrolytes, in this study were synthesized from styrene-maleic anhydride (SMA) copolymer, poly(ethylene glycol)400 (PEG400), and lithium perchlorate (LiClO4). Fourier transform infrared spectroscopy (FTIR), and magic angle spinning (MAS) solid-state NMR were used to monitor the interaction between Li+ ions and polymer. The results of FTIR and MAS solid-state NMR indicate the Li+ ions are preferentially coordinated to the ether oxygen of PEG. The Tg of the PEG segments in polyelectrolyte increases with LiClO4 concentration, as determined by differential scanning calorimetry (DSC), indicating that solubility of the Li+ ions in the host polymer increases with the PEG content. Impedance spectroscopy (IS) shows that the bulk conductivity of polyelectrolytes and the conductivity behavior obeys the Vogel-Tamman-Fulcher (VTF) equation. 相似文献
47.
Spherical NiO-C composite was prepared by dispersing spherical NiO in glucose solution and subsequent carbonization under hydrothermal conditions at 180 °C. The microstructure and morphology of the NiO-C and NiO powders were characterized by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical properties of the electrodes were measured by galvanostatic charge-discharge tests, cyclic voltammetric analysis (CV), and electrochemical impedance spectroscopy (EIS). SEM images showed that the amorphous carbon not only coated on the surface but also filled the inner pores of the NiO spheres. Electrochemical tests showed that the NiO-C composite exhibited higher initial coulombic efficiency (66.6%) than NiO (56.4%), and better cycling performances. The improvement of these properties is attributed to the carbon, as it can reduce the specific surface area of porous sphere, and enhance the conductivity of porous NiO. 相似文献
48.
The electrochemical behavior of Li/V6O13 cells is investigated at room temperature (22 °C) both in liquid electrolyte consisting of oligomeric poly(ethyleneglycol)dimethylether+lithium bis(trifluoromethylsulfonylimide) and composite electrolytes formed by blending the liquid electrolyte with silica nanoparticles (fumed silica). The addition of fumed silica yields a gel-like electrolyte that demonstrates the desirable property of suppressing lithium dendrite growth due to the rigidity and immobility of the electrolyte structure. The lithium/electrolyte interfacial resistance for composite gel electrolytes is less than that for the corresponding base-liquid electrolyte, and the charge-discharge cycle performance and electrochemical efficiency for the Li/V6O13 cell is significantly improved. The effect of fumed silica surface group on the electrochemical performance is discussed; the native hydrophilic silanol surface group appears better than fumed silica that is modified with a hydrophobic octyl surface moiety. 相似文献
49.
New lithium nickel nitrides Li3−2xNixN (0.20 ≤ x ≤ 0.60) have been prepared and investigated as negative electrode in the 0.85/0.02 V potential window. These materials are prepared from a Ni/Li3N mixture at 700 °C under a nitrogen flow. Their structural characteristics as well as their electrochemical behaviour are investigated as a function of the nickel content. For the first time are reported here the electrochemical properties of a lithium intercalation compound based on a layered nitride structure. The Li3−2xNixN compounds can be reversibly reduced and oxidized around 0.5 V versus Li/Li+ leading to specific capacities in the range 120-160 mAh/g depending on the nickel content and the C rate. Due to a large number of lithium vacancies, the structural stability provides an excellent capacity retention of the specific capacity upon cycling. 相似文献
50.
A study on capacity fading of lithium-ion battery with manganese spinel positive electrode during cycling 总被引:3,自引:0,他引:3
The capacity fading mechanism of lithium-ion cell was studied by disassembling the charge-discharged cells and analyzing their electrodes using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS), etc. Cu ion dissolved from current collector of anode and Mn ion dissolved from LiMn2O4 spinel (cathode) were all existing in solid electrolyte interface (SEI) layer on carbon anode as Cu2O and MnO or MnO2, respectively. These depositions of Cu and Mn oxides did not uniformly deposited on the anode side, and most of them were detected on the carbon surface nearby to the separator side. The SEI layer is hard and about 0.3 μm in thickness. Furthermore, the cycling performance of the cells can be improved by adding 1,2,3-benzotrazole (a corrosion inhibitor of Cu) before assembling the cell, it then coordinates strongly with Cu ions into the electrolyte. From the results, it is obvious that the existing of Cu oxide as well as Mn oxide in the SEI layer, which blocks the normal intercalation of the lithium ions, is one of the factors for the capacity fading of the cells. 相似文献