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Alternative route for LiFePO4 synthesis: Carbothermal reduction combined with microwave-assisted solid-state reaction

机译:LiFePO4合成的替代方法:碳热还原与微波辅助固态反应相结合

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LiFePO4 was synthesized via a microwave-assisted solid-state reaction. The precursors LiOH center dot H2O, FePO4 center dot 4H(2)O, glucose, and graphite were first subjected to carbothermal reduction at 200 degrees C during 3 h and subsequently calcined under microwave irradiation at 800 W for very short times varying from 1 to 5 min. The products obtained at different microwave calcination times were systematically investigated through thermal (TGA-DTG and DSC), structural (XRD), morphological (SEM), and electrochemical (cyclic voltammetry) analyses. The best results were attained for the product obtained at the microwave calcination time of 3 min: smallest particle size (majority in the range of 100-150 nm), crystallographic pattern of LiFePO4 and some by-products, and voltammetric profile characteristic of LiFePO4. Thus, the here-presented synthesis methodology implies a significant reduction in processing time while yielding LiFePO4 nanoparticles with good electrochemical activity for the Li ion intercalation process. (C) 2016 Elsevier Ltd. All rights reserved.
机译:LiFePO4是通过微波辅助固态反应合成的。首先对前体LiOH中心点H2O,FePO4中心点4H(2)O,葡萄糖和石墨进行碳热还原反应,在3小时内于200摄氏度进行碳热还原,然后在800 W的微波辐射下煅烧非常短的时间(从1到1)。 5分钟。通过热(TGA-DTG和DSC),结构(XRD),形态(SEM)和电化学(循环伏安)分析系统地研究了在不同微波煅烧时间下获得的产物。对于在3分钟的微波煅烧时间下获得的产品,可获得最佳结果:最小的粒径(多数在100-150 nm范围内),LiFePO4和一些副产物的结晶图谱以及LiFePO4的伏安曲线特征。因此,本文提出的合成方法暗示了处理时间的显着减少,同时产生了对Li离子嵌入过程具有良好电化学活性的LiFePO4纳米颗粒。 (C)2016 Elsevier Ltd.保留所有权利。

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