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CoNi2S4 Nanoplate Arrays Derivedfrom Hydroxide Precursors for Flexible Fiber-Shaped Supercapacitors

机译:CoNi2S4纳米板阵列用于柔性纤维状超级电容器的氢氧化物前驱物

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摘要

A high-quality porous CoNi2S4 nanoplates array was in situ synthesized on carbon fibers (CFs) by a hydrothermal method via a CoNi-layered double hydroxide (LDH) precursor transformation process. The CoNi2S4@CFs electrode exhibits largely enhanced supercapacitor performance with a specific capacitance of 1724 F/g at 1 A/g, in comparison with that of the CoNi-LDH (1302 F/g) precursor. Furthermore, the CoNi2S4@CF electrode shows an extremely high rate capability with capacity retention of 79% under a charge density of 60 A/g, whereas the retention rate of CoNi-LDH@CFs is only ∼34%. The abundant pore structure, improved electrical conductivity, and lower internal resistances of CoNi2S4@CFs (1.0 Ω) compared to those of CoNi-LDH@CFs (9.5 Ω) are responsible for the enhancement of energy storage performance. By using the CoNi2S4 nanoplate array as the positive electrode, an all-solid-state asymmetric fiber-shaped supercapacitor was further obtained, which exhibits outstanding flexible, foldable, and wearable capability. In view of the component tunability for LDH materials, the hydroxideprecursor transformation method with merits of mild conditions andeasy operation can be extended to the synthesis of a variety of metalsulfides for broad applications in electronic devices.
机译:通过CoNi层状双氢氧化物(LDH)前体转化过程,通过水热法在碳纤维(CFs)上原位合成了高质量的多孔CoNi2S4纳米板阵列。与CoNi-LDH(1302 F / g)前驱体相比,CoNi2S4 @ CFs电极在1 A / g时的比电容为1724 F / g时,超级电容器性能大大提高。此外,CoNi2S4 @ CF电极在60 A / g的电荷密度下显示出极高的倍率能力,容量保持率为79%,而CoNi-LDH @ CFs的保持率仅为〜34%。与CoNi-LDH @ CFs(9.5Ω)相比,CoNi2S4 @ CFs(1.0Ω)具有丰富的孔结构,改善的电导率和更低的内阻,这有助于提高储能性能。通过使用CoNi2S4纳米板阵列作为正电极,进一步获得了全固态不对称纤维状超级电容器,该电容器具有出色的柔韧性,可折叠性和耐磨性。考虑到LDH材料的组分可调性,氢氧化物具有温和条件和操作简便,可扩展到多种金属的合成硫化物,广泛用于电子设备。

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