首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Rapid Microwave-Assisted Solvothermal Synthesis of Non-Olivine Cmcm Polymorphs of LiMPO4 (M = Mn, Fe, Co, and Ni) at Low Temperature and Pressure
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Rapid Microwave-Assisted Solvothermal Synthesis of Non-Olivine Cmcm Polymorphs of LiMPO4 (M = Mn, Fe, Co, and Ni) at Low Temperature and Pressure

机译:低温低压快速微波辅助溶剂热合成LiMPO4(M = Mn,Fe,Co和Ni)非橄榄石Ccmm多晶型物

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Lithium transition-metal phosphates, LiMPO4 (M = Mn, Fe, Co, and Ni), have attracted significant research interest over the past two decades as an important class of lithium ion battery cathode materials. However, almost all of the investigations thus far have focused on the olivine polymorph that exists in the orthorhombic Pnma space group. In this study, a distinct orthorhombic but non-olivine polymorph of LiMPO4, described by a Cmcm space group symmetry, has been synthesized with M = Mn, Fe, Co, and Ni. Of these, LiMnPO4 in the Cmcm space group is reported for the first time. A rapid microwave-assisted solvothermal (MW-ST) heating process with tetraethylene glycol (TEG) as the solvent and transition-metal oxalates as precursors facilitates the synthesis of these materials. The peak reaction temperatures and pressures were below 300 degrees C and 30 bar, respectively, which are several orders of magnitude lower than those of the previously reported high-pressure (gigapascals) method. X-ray diffraction (XRD) confirms the crystal structure with the Cmcm space group, and scanning electron micrographs indicate a submicrometer thin platelet-like morphology. The synthesis process conditions have been optimized to obtain impurity-free samples with the correct stoichiornetry, as characterized by XRD and inductively coupled plasma-optical emission spectroscopy (ICP-OES). Upon heat treatment to higher temperatures, an irreversible transformation of the metastable Cmcm polymorphs into olivine is observed by XRD and Fourier transform infrared spectroscopy. Although the electrochemical activity of these polymorphs as lithium ion cathodes turns out to be poor, the facile synthesis under mild conditions has permitted easy access to these materials in a nanomorphology, some of which were not even possible before.
机译:锂过渡金属磷酸盐LiMPO4(M = Mn,Fe,Co和Ni)作为锂离子电池正极材料的重要一类,在过去的二十年中引起了广泛的研究兴趣。但是,到目前为止,几乎所有的研究都集中在正交晶体Pnma空间群中存在的橄榄石多晶型物上。在这项研究中,已合成出一种由Mcm,Mn,Fe,Co和Ni组成的,由Ccmm空间群对称性描述的LiMPO4的正交晶但非橄榄石的多晶型物。其中,Cmcm空间群中的LiMnPO4首次被报道。快速微波辅助溶剂热(MW-ST)加热工艺,以四甘醇(TEG)为溶剂,过渡金属草酸盐为前体,有助于这些材料的合成。峰值反应温度和压力分别低于300摄氏度和30巴,比以前报道的高压方法(千兆帕斯卡)要低几个数量级。 X射线衍射(XRD)确认具有Cmcm空间基团的晶体结构,而扫描电子显微照片则显示出亚微米级的薄薄片状形态。通过XRD和电感耦合等离子体发射光谱(ICP-OES)对合成工艺条件进行了优化,以获得具有正确化学计量的无杂质样品。在热处理至更高的温度后,通过XRD和傅里叶变换红外光谱观察到亚稳态Cmcm多晶型物不可逆转变为橄榄石。尽管这些多晶型物作为锂离子阴极的电化学活性被证明很差,但在温和条件下的简便合成已允许以纳米形态轻松获得这些材料,其中有些甚至以前是不可能的。

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