三维Ni/NiO@C/GN复合材料的制备及其锂离子电池性能

Preparation and performance of a graphene-(Ni-NiO)-C hybrid as the anode of a lithium-ion battery

  • 摘要: 将醋酸镍和葡萄糖溶于水中,与氧化石墨烯(GO)水悬浮液均匀混合,在180 °C下水热处理24 h,再在Ar中700 °C下炭化3 h,然后在空气中300 °C下煅烧3 h得到三维Ni/NiO@C/GN。结果表明,水热处理过程中葡萄糖衍生的炭层将Ni(OH)2完全包裹,并在炭化过程中转化为金属Ni,部分金属Ni在空气中煅烧中被氧化为NiO。当作为锂离子电池的负极材料时,其初始容量为711.6 mA h g−1,300次循环后增加到772.1 mA h g−1。作为对比,没有添加GO的材料的初始容量较低,仅为584.7 mA h g−1,300次循环后下降到148.8 mA h g−1。这些结果表明炭层可以抑制Ni/NiO纳米颗粒的团聚,有效缓解锂化过程中的体积膨胀,抑制循环过程中的电极开裂。GO的加入可形成丰富的导电网络,提高导电性。较大的比表面积可增加活性位点,有利于电解液快速浸润电极材料。这些因素显著改善了Ni/NiO@C/GN负极的电化学性能。

     

    Abstract: A graphene-(Ni-NiO)-C hybrid was prepared by dissolving nickel acetate and glucose in water to form a solution that was mixed with a graphene oxide (GO) aqueous suspension, hydrothermally treated at 180 °C for 24 h, carbonized at 700 °C for 3 h in Ar and calcined at 300 °C for 3 h in air. Results indicated that Ni(OH)2 formed during the hydrothermal treatment was converted to metallic Ni during carbonization, which was partly oxidized to NiO during calcination. When used as the anode material of a lithium-ion battery, it had a high initial capacity of 711.6 mA h g−1, which increased to 772.1 mA h g−1 after 300 cycles. For comparison, the sample without added GO had a much lower initial capacity of 584.7 mA h g−1, which decreased to 148.8 mA h g−1 after 300 cycles. Hybridization of the Ni-NiO nanoparticles with carbon inhibited their aggregation. The GO addition led to the formation of a conducting network, which alleviated the large volume expansion during lithiation, prevented the electrode from cracking during cycling and increased the surface area for easy access of the electrolyte. These factors jointly contributed to the obvious improvement in the electrochemical performance of the graphene-(Ni-NiO)-C anode.

     

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