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Structural, magnetic and electrochemical properties of lithium iron orthosilicate

机译:硅酸锂铁的结构,磁性和电化学性质

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We report the structural and electronic characterization of Li_2FeSiO_4 synthesized by solid-state reaction. X-ray diffraction, Raman scattering, Fourier transform infrared (FTIR) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy and magnetization measurements are analyzed. Magnetic susceptibility experiments give evidence that Li_2FeSiO_4 powders possess an antiferromagnetic ordering below T_N = 25 K due to long range Fe-O-Li-O-Fe interactions. Analysis of the paramagnetic region giving the Curie-Weiss parameters theta_p = -93.5 K and C_p = 4.13 emu K mol~(-1) shows the divalent state of Fe cations. Electron paramagnetic resonance experiments confirm this electronic configuration. Electrochemical measurements were carried out in lithium cells with LiTFSI in a poly(ethylene oxide) (PEO) polymer electrolyte at 80 deg C. The resulting cyclic voltammogram indicates a stable structure for the first cycle with redox peaks at 2.80 and 2.74 V versus Li~0/Li~+.
机译:我们报告了固态反应合成的Li_2FeSiO_4的结构和电子表征。分析了X射线衍射,拉曼散射,傅立叶变换红外(FTIR)光谱,电子顺磁共振(EPR)光谱和磁化强度测量。磁化率实验表明,由于长距离的Fe-O-Li-O-Fe相互作用,Li_2FeSiO_4粉末在T_N = 25 K以下具有反铁磁有序。给出居里-魏斯参数theta_p = -93.5 K和C_p = 4.13 emu K mol〜(-1)的顺磁区分析表明Fe阳离子为二价态。电子顺磁共振实验证实了这种电子结构。电化学测量是在80°C的聚环氧乙烷(PEO)聚合物电解质中,用LiTFSI在锂电池中进行的。所得循环伏安图显示了第一个循环的稳定结构,相对于Li〜,氧化还原峰在2.80和2.74 V 0 / Li〜+。

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