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聚吡咯包覆FeCl3-石墨层间化合物的制备与电化学储钠性能
引用本文:柳小玄,韩飞,刘洪波,刘金水.聚吡咯包覆FeCl3-石墨层间化合物的制备与电化学储钠性能[J].复合材料学报,2021,38(11):3818-3826.
作者姓名:柳小玄  韩飞  刘洪波  刘金水
作者单位:湖南大学  材料科学与工程学院,长沙 410082
基金项目:湖南省科技创新人才计划项目(2020RC3023);湖南省科技重大专项项目(2018GK1030);湖南大学汽车车身先进设计制造国家重点实验室人才培育项目(51965010)
摘    要:以FeCl3和天然鳞片石墨为原料,通过融盐法制得1阶FeCl3插层的石墨层间化合物(FeCl3-GIC)。用原位聚合法对FeCl3-GIC进行聚吡咯(PPy)包覆改性,形成具有核壳结构的(FeCl3-GIC)@PPy复合材料。通过多种表征方法研究聚吡咯包覆前后FeCl3-GIC的表面形貌和微观结构变化。结果表明:聚吡咯均匀致密地包覆在十微米级的FeCl3-GIC颗粒外部,包覆层厚度为35 nm,经过聚吡咯包覆后(FeCl3-GIC)@PPy的导电性能显著提高((FeCl3-GIC)@PPy粉末电阻率2.3×10?3 Ω·cm,FeCl3-GIC粉末电阻率3.1×10?3 Ω·cm)。采用多种电化学测试探究产物的钠离子存储特性,聚吡咯外壳能够显著提高FeCl3-GIC作为钠离子电池负极材料的充放电容量、倍率性能和循环性能。在0.1 A·g?1电流密度下循环100次后,FeCl3-GIC的比容量逐渐衰减到157 mA·h·g?1,而(FeCl3-GIC)@PPy材料的比容量达到281 mA·h·g?1左右且容量基本保持不变;在电流密度1 A·g?1的条件下循环500次后,(FeCl3-GIC)@PPy的比容量仍有181 mA·h·g?1,容量保持率约为89%。 

关 键 词:聚吡咯    石墨层间化合物    氯化铁    钠离子存储    二次电池
收稿时间:2020-11-24

Preparation and electrochemical sodium storage performance of polypyrrole coated FeCl3-intercalated graphite intercalation compound
Affiliation:College of Materials Science and Engineering, Hunan University, Changsha 410082, China
Abstract:The 1-stage FeCl3-intercalated graphite intercalation compound (FeCl3-GIC) were prepared by a molten salt method using FeCl3 and natural flake graphite as raw materials. Subsequently, a conductive layer of polypyrrole (PPy) were uniformly coated on the surface of the FeCl3-GIC particles by in-situ polymerization to form a core-shell structured (FeCl3-GIC)@PPy composite material. Various characterization methods were employed to study the surface morphology and microstructure evolution of FeCl3-GIC before and after polypyrrole coating. The results show that a uniform and dense polypyrrole layer with a thickness of 35 nm is tightly coated on the surface of the micro-sized FeCl3-GIC particles. After coating, the conductivity of the (FeCl3-GIC)@PPy composite is significantly improved for the powder resistivity is reduced from 3.1×10?3 Ω·cm of FeCl3-GIC to 2.3×10?3 Ω·cm of (FeCl3-GIC)@PPy. As an anode material for sodium ion storage, it is found that the (FeCl3-GIC)@PPy anode exhibits the improved reversible capacitiy, rate capability and cycling stability compared with the naked FeCl3-GIC anode. Specially, the specific capacity of (FeCl3-GIC)@PPy remains steady with a high sodium storage value of 281 mA·h·g?1 after 100 cycles at the current density of 0.1 A·g?1, while the FeCl3-GIC anode shows a continuous capacity decay with a low value of 157 mA·h·g?1 after 100 cycles. Additionally, even at a high current density of 1.0 A·g?1, the (FeCl3-GIC)@PPy anode delivers a remained sodium storage capacity of 181 mA·h·g?1 after 500 cycles, accompanying with a fascinating capacity retention ratio of 89%. 
Keywords:
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