Yang Gang, Wang Guan, Hou Wenhua
Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, People's Republic of China.
J Phys Chem B. 2005 Jun 9;109(22):11186-96. doi: 10.1021/jp050448s.
A novel and economical microwave route has been developed for the synthesis of electrochemically active LiV(3)O(8) material by using a domestic microwave oven. The heating behavior of the designed reaction system guided the preparation of LiV(3)O(8) at a suitable irradiation power (i.e. heating rate), reaction time, and temperature. At the lowest irradiation power, the conversion fraction of reactants was mainly controlled by reaction temperature. Characterization results of X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Raman spectroscopy, scanning (SEM) and transmission (TEM) electron microscopy, and BET surface areas indicated that the phases of samples prepared by microwave and traditional methods were in good agreement. Nevertheless, the crystallinity, crystallite configuration, and morphology of the samples were different, and were affected by the irradiation time and power. A floppy superposition structure of nanosheets (the size of one nanosheet was about 4.5 microm x 1.2 microm x 3 nm) was preferentially grown at the lowest irradiation power, and this effect on structure was more in evidence as the nanorods formed at the highest irradiation power. Electrochemical studies on ionic conductivity, electrochemical impedance spectroscopy (EIS), and charge-discharge capacity were carried out. It was found that the conductivity, first discharge capacity, and cycle performances of the samples were affected by the crystal size, crystallinity, and crystal configuration and defection concentration. The sample L30 prepared at the lowest irradiation power and the shortest time (30 min) showed the highest discharge capacity (335 mAh/g), but its discharge capacity decreased rapidly. By comparison, the sample L100 had a floppy superposition structure of nanosheets and a high surface area, provided a good two-dimensional channel for the transition of Li(+) ions, and was stable during the intercalation/deintercalation process of Li(+) ions, therefore the high ionic conductivity, high discharge capacity, and good cycle performance were presented. The relationship between the electrochemical properties and the irradiation power was discussed.
通过使用家用微波炉,已开发出一种新颖且经济的微波路线来合成具有电化学活性的LiV(3)O(8)材料。所设计反应体系的加热行为指导了在合适的辐照功率(即加热速率)、反应时间和温度下制备LiV(3)O(8)。在最低辐照功率下,反应物的转化分数主要受反应温度控制。X射线衍射(XRD)、傅里叶变换红外(FTIR)和拉曼光谱、扫描(SEM)和透射(TEM)电子显微镜以及BET表面积的表征结果表明,通过微波法和传统方法制备的样品相吻合良好。然而,样品的结晶度、微晶构型和形态不同,且受辐照时间和功率影响。在最低辐照功率下优先生长出纳米片的松散叠加结构(一个纳米片的尺寸约为4.5微米×1.2微米×3纳米),随着在最高辐照功率下形成纳米棒,这种对结构的影响更为明显。进行了关于离子电导率、电化学阻抗谱(EIS)和充放电容量的电化学研究。发现样品的电导率、首次放电容量和循环性能受晶体尺寸、结晶度、晶体构型和缺陷浓度影响。在最低辐照功率和最短时间(30分钟)下制备的样品L30显示出最高放电容量(335 mAh/g),但其放电容量迅速下降。相比之下,样品L100具有纳米片的松散叠加结构和高比表面积,为Li(+)离子的迁移提供了良好的二维通道,并且在Li(+)离子的嵌入/脱嵌过程中稳定,因此表现出高离子电导率、高放电容量和良好的循环性能。讨论了电化学性质与辐照功率之间的关系。