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1.
侯贤华  胡社军  石璐 《物理学报》2010,59(3):2109-2113
采用磁控溅射沉积技术制备了纳米级Sn-Ti合金负极材料,并用X射线衍射和扫描电子显微镜进行表征,用高精度电池测试系统进行充放电和循环伏安测试.结果表明先镀Sn后镀Ti(Sn/Ti复合膜)和先镀Ti后镀Sn(Ti/Sn复合膜)具有很大的性能差异,其中Sn/Ti复合膜具有优异的循环稳定性和较高的可逆容量.首次放电容量和充电容量分别为9275 mAh/g和6954 mAh/g,首次库仑效率为75%,经30次循环后,该电极的放电容量保持为4152 mAh/g,这主要归因于活性物质Sn与电解液界面之间存在非活 关键词: 锂离子电池 磁控溅射 Sn-Ti合金 电化学性能  相似文献   

2.
李娟  汝强*  孙大伟  张贝贝  胡社军  侯贤华 《物理学报》2013,62(9):98201-098201
以酸处理的中间相碳微球(MCMB)为载体, 用化学还原法在碳球表面沉积SnSb合金, 合成SnSb 包覆碳球的核壳结构负极材料. 采用XRD, SEM技术对材料的结构和形貌进行了表征, 用恒电流充放电(CC)、循环伏安(CV)和交流阻抗(EIS)测试了材料的电化学性能. 实验结果表明: SnSb/MCMB样品呈现纳米晶与非晶态的混合组织; 单一SnSb合金的容量衰减较快, 而对于SnSb/MCMB复合材料, 细小的合金颗粒均匀钉扎在MCMB表面, 不仅改善了颗粒的团聚现象, 而且增强了材料的导电能力, 使材料的循环稳定性得到改善, 复合材料具有936.161 mAh/g的首次放电比容量, 首次库仑效率80.3%, 50次循环后容量维持在498.221 mAh/g. 关键词: SnSb合金 锂离子电池 中间相碳微球(MCMB) 电化学性能  相似文献   

3.
彭薇  岳敏  梁奇  胡社军  侯贤华 《物理学报》2011,60(3):38202-038202
本文采用固相法制备了纯相LiMn1-xFexPO4/C (x=0.2,0.4,0.6)正极材料,并用X射线衍射(XRD)和扫描电镜(SEM)进行表征,用高精度电池测试系统进行充放电和循环伏安测试.结果表明不同Mn和Fe原子比的电极材料具有很大的性能差异,其中当x=0.4时,材料具有优异的循环稳定性和较高的可逆容量.首次充电容量和放电容量分别达到141.5 mAh/g和125.7 mAh 关键词: 锂离子电池 固相法 1-xFexPO4')" href="#">LiMn1-xFexPO4 正极材料  相似文献   

4.
采用改进的Hummers 法, 以石墨粉为原料制备氧化石墨, 然后使用微波还原法制备石墨烯, 最后以石墨烯作为负极材料组装锂离子电池. 系统的研究了高温氧化阶段中温度对氧化石墨的氧化程度、石墨烯的还原程度和比表面积以及锂离子电池性能的影响. 利用场发射扫描电镜(FESEM)、 X射线光电子能谱(XPS)、X射线衍射仪(XRD)、BET测量仪对氧化石墨和石墨烯的微观结构及比表面积等进行测试和表征. XRD, XPS及电化学测试的结果显示当高温阶段氧化温度为90 °C时, 氧化石墨的氧化程度最高, 相应的石墨烯也具有最高的还原程度和最大的比表面积423.2 m2/g, 同时石墨烯锂离子电池也具有更好的性能: 首次放电比容量为1555.5 mAh/g, 充电容量为1024.6 mAh/g, 其循环放电比容量达到600 mAh/g.  相似文献   

5.
采用离子束辅助沉积法制备了锂离子电池硅薄膜负极材料,研究了硅薄膜的晶体结构、表面形貌和电化学性能.研究结果表明:硅薄膜是非晶态的结构;非晶态硅薄膜发生嵌脱锂反应的电位分别为0.03 V与0.34 V和0.16 V与0.49 V;硅薄膜表现出很高比容量和充放电效率,其可逆比容量和库仑效率分别为3134.4 mAh/g和87.1%;硅薄膜具有优异的循环性能,在0.5C倍率下200次循环后容量保持率为92.2%. 关键词: 硅薄膜 离子束辅助沉积 锂离子电池 负极材料  相似文献   

6.
首次报道了用 35 5nm脉冲激光沉积非晶态Ni V2 O5复合薄膜电极的电化学性能 .采用不同摩尔比的NixV2 O5靶 (x =0 .1,0 .3,0 .5 ) ,在不同的基片温度 (Ts)和O2 气压力下制备了Ni V2 O5复合薄膜 .XRD和SEM测定表明 ,在不锈钢基片上 ,Ts=30 0℃和氧气压力为 14Pa沉积 0 .5h得到的是非晶态的Ni V2 O5薄膜 .将此非晶态的Ni0 .3 V2 O5薄膜电极用于锂电池的正极 ,与纯V2 O5薄膜相比 ,不仅具有良好的放电速率性能和高的比容量 ,而且其充放电循环稳定性优异 .该薄膜电极在放电速率为 2 0C时测得的比容量达 2 0 0mAh/ g ,并经 10 0 0次以上的充放电循环无明显的衰减  相似文献   

7.
通过热聚合法成功制备出纳米级Li3V2(PO43/C正极材料,中间产物和最终材料的Li3V2(PO43/C颗粒均小于200 nm,无定形碳的含量为4.6%,处于Li3V2(PO43颗粒表面和颗粒与颗粒之间.该材料在3.0sim4.3 V和0.1 C电流下放电比容量为124 mAh/g,100次循环之后无衰减,表现出较好的循环性能.其倍率性能优异,在3.0sim4.3 V和20 C的条件下放电比容量达到80 mAh/g,在3.0sim4.8 V和10 C的条件下放电比容量达到100 mAh/g.  相似文献   

8.
陈畅  汝强  胡社军  安柏楠  宋雄 《物理学报》2014,63(19):198201-198201
实验首先采用改进的Hummers法制备氧化石墨,然后以氧化石墨烯为前驱体,通过水热法将锡酸钴纳米颗粒均匀镶嵌在石墨烯薄膜基片上,最终获得Co2SnO4/Graphene镶嵌复合材料. 采用X射线衍射(XRD)、扫描电子显微镜(SEM)对材料的结构和形貌进行表征,通过恒电流充放电(CC)、循环伏安法(CV)与交流阻抗法(EIS)测试了材料的电化学性能. 实验结果表明,石墨烯良好的分散性及较高的电子导电率,可以提高锡酸钴材料的电化学性能,材料首次可逆容量达到1415.2 mA·h/g,50次循环后仍能保持469.7 mA·h/g的放电比容量. 关键词: 2SnO4')" href="#">Co2SnO4 石墨烯 电化学性能 锂离子电池  相似文献   

9.
实验首先采用改进的Hummers法制备氧化石墨,然后以氧化石墨烯为前驱体,通过水热法将锡酸钴纳米颗粒均匀镶嵌在石墨烯薄膜基片上,最终获得Co2SnO4/Graphene镶嵌复合材料.采用X射线衍射(XRD)、扫描电子显微镜(SEM)对材料的结构和形貌进行表征,通过恒电流充放电(CC)、循环伏安法(CV)与交流阻抗法(EIS)测试了材料的电化学性能.实验结果表明,石墨烯良好的分散性及较高的电子导电率,可以提高锡酸钴材料的电化学性能,材料首次可逆容量达到1415.2 mA·h/g,50次循环后仍能保持469.7 mA·h/g的放电比容量.  相似文献   

10.
通过V2O5的碳热还原反应制备了具有优异倍率性能和循环稳定性的V2O3-C双层包覆的磷酸铁锂正极材料. 粉末X射线衍射、元素分析、高分辨投射电镜和拉曼光谱研究表明V2O3相与碳层共包覆于磷酸铁锂颗粒表面. 在V2O5的碳热还原反应后,碳含量明显降低,但石墨化程度未发生明显改变. 电化学测试结果表明少量V2O3显著改善了磷酸铁锂正极材料的倍率性能和高温循环性能,包含1%氧化钒的复合正极材料在0.2 C放电容量为167 mAh/g,5 C时放电容量为129 mAh/g,并且循环稳定性优异;在55 oC和1 C时放电容量为151 mAh/g,循环100次后无明显容量衰减.  相似文献   

11.
Focusing on additive-free electrodes, thin films are of typical interest as electrodes for lithium ion battery application. Herein, we report the fabrication of TiO2 thin films by spray pyrolysis deposition technique. X-ray diffraction and transmission electron microscopic analysis confirms the formation of anatase TiO2. Electrochemical evaluation of these sub-micron TiO2 thin films exhibits high-rate performance and long cycling stability. At 1C rate (1C?=?335 mA/g), the electrode delivered discharge capacity of 247 mAh/g allowing about 0.74 lithium into the structure. The electrodes also delivered specific capacities of 122 and 72 mAh/g at 10 and 30C rates, respectively. Without conductive additives, this excellent performance can be attributed to the nanosize effect of TiO2 particles combined with the uniform porous architecture of the electrode. Upon cycling at high rates (10 and 30C), the electrode exhibited excellent cycling stability and retention, specifically only <?0.6% capacity loss per cycle over 2500 cycles.  相似文献   

12.
The oil in water (o/w) emulsions were prepared using aniline dissolved in toluene and LiCoO2 particles as stabilizers (Pickering emulsions). Pickering emulsions are stabilized by adsorbed solid particles instead of emulsifier molecules. The mean droplet diameter of emulsions was controlled by the mass ratio M (oil)/M (solid particles). The emulsions showed great stability during 3 days. The composite materials containing LiCoO2 and the conductive polymer polyaniline (PANI) have been prepared by means of polymerization of aniline emulsion stabilized by LiCoO2 particles. The composite materials were characterized by nanosphere and nanofiber-like structures. The nanofiber-like morphology of the powdered material was distinctly different of the morphologies of the parent materials. The electrochemical reactivity of PANI/LiCoO2 composites as positive electrode in a lithium battery was examined during lithium ion deinsertion and insertion by galvanostatic charge–discharge testing; PANI/LiCoO2 (1:4) composite materials exhibited the best electrochemical performance by increasing the reaction reversibility and capacity compared to that of the pristine LiCoO2 cathode. The first discharge capacity of PANI/LiCoO2 (1:4) was 167 mAh/g, while that of LiCoO2 was136 mAh/g.  相似文献   

13.
The layered Li-rich Mn-based cathode materials Li[Li0.2Mn0.54Ni0.13Co0.13]O2 were prepared by using co-precipitation technique at different temperatures, and their crystal microstructure and particle morphology were observed and analyzed by XRD and SEM. The electrochemical properties of these samples were investigated by using charge-discharge tests, electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV), respectively. The results indicated that all samples are of high purity. When the precursors were co-precipitated at 50 °C, their cathode materials have the most uniform and full particles and exhibit the highest initial discharge capacity (289.4 mAh/g at 0.1C), the best cycle stability (capacity retention rate of 91.2 % after 100 cycles at 0.5C), and the best rate performance. The EIS results show that the lower charge transfer resistance of 50 °C sample is responsible for its superior discharge capacity and rate performance.  相似文献   

14.
Fengling Chen 《中国物理 B》2022,31(7):78101-078101
One of the major hurdles of nickel-rich cathode materials for lithium-ion batteries is the low cycling stability, especially at high temperature and high voltage, originating from severe structural degradation, which makes this class of cathode less practical. Herein, we compared the effect of single and dual ions on electrochemical performance of high nickel (LiNi0.88Mn0.03Co0.09O2, NMC) cathode material in different temperatures and voltage ranges. The addition of a few amounts of tantalum (0.2 wt%) and boron (0.05 wt%) lead to improved electrochemical performance. The co-modified LiNi0.88Mn0.03Co0.09O2 displays an initial discharge capacity of 234.9 mAh/g at 0.1 C and retained 208 mAh/g at 1 C after 100 cycles at 45 ℃, which corresponds to a capacity retention of 88.5%, compared to the initial discharge capacity of 234.1 mAh/g and retained capacity of 200.5 mAh/g (85.6%). The enhanced capacity retention is attributed to the synergetic effect of foreign elements by acting as a surface structural stabilizer without sacrificing specific capacity.  相似文献   

15.
《Current Applied Physics》2019,19(8):902-909
Carbon matrices have attracted the attention enthusiastically as the improver materials of sulfur for rechargeable lithium-sulfur battery. In this work, various morphologies (sphere, fiber, tube and layer) based carbon materials have been used for preparing the sulfur-carbon binary composites via melt diffusion method for lithium-sulfur battery application. The prepared binary composites have been characterized for its structural and morphological information using X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, and, Scanning and Transmission electron microscopy. The electrochemical studies are characterized by cyclic voltammetry, charge-discharge and cycle life after being assembled as lithium-sulfur cell. The S-prGO composite exhibits the initial discharge capacity of 893 mAh g−1 and it sustains over 50 cycles (598 mAh g−1) at 0.1C, with low capacity fading rate when compared to the other composites studied. A remarkable electrochemical performance indicates that the sheet like morphology can accommodate the volume expansion of sulfur and the oxygen groups containing GO minimize the dissolution of lithium polysulfides.  相似文献   

16.
Electrospraying-based synthesis of NiCo2O4 (NCO-ES) nanoparticles that exhibit long cycle life and high rate capability is reported. The results are compared with a conventionally prepared NiCo2O4 sample by direct annealing (NCO-DA). The structure and morphology of NCO-ES and NCO-DA nanoparticles have been characterized by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy to confirm the size, morphology, structure, and surface chemistry of the as-prepared samples. Electrochemical testing established that the NCO-ES sample displayed enhanced Li-ion storage performance. The NCO-ES delivered a discharge capacity of almost 370 mAh/g at the end of 50 cycles at 1C rate (890 mA/g) while only 180 mAh/g was retained for the NCO-DA sample at the same condition. At a high rate of 5C (4450 mA/g), NCO-ES electrodes delivered a stabilized specific capacity of 225 mAh/g with almost 100% Coulombic efficiency over 1000 cycles. Its rate capability and cycle life were found to be superior to NCO-DA electrodes. The nanoscale grain boundaries in the NCO-ES sample enhanced the lithium-ion diffusion and enabled high rate capability. The impedance analysis at different stages of lithiation/delithiation indicates a lower impedance and better kinetics as one of the reasons for better performance of the NCO-ES sample.  相似文献   

17.
Fengling Chen 《中国物理 B》2022,31(5):58101-058101
Nickel-rich cathode materials are increasingly being applied in commercial lithium-ion batteries to realize higher specific capacity as well as improved energy density. However, low structural stability and rapid capacity decay at high voltage and temperature hinder their rapid large-scale application. Herein, a wet chemical method followed by a post-annealing process is utilized to realize the surface coating of tantalum oxide on LiNi0.88Mn0.03Co0.09O2, and the electrochemical performance is improved. The modified LiNi0.88Mn0.03Co0.09O2 displays an initial discharge capacity of ~ 233 mAh/g at 0.1 C and 174 mAh/g at 1 C after 150 cycles in the voltage range of 3.0 V-4.4 V at 45℃, and it also exhibits an enhanced rate capability with 118 mAh/g at 5 C. The excellent performance is due to the introduction of tantalum oxide as a stable and functional layer to protect the surface of LiNi0.88Mn0.03Co0.09O2, and the surface side reactions and cation mixing are suppressed at the same time without hampering the charge transfer kinetics.  相似文献   

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