Investigation of energy storage performance in organic molecule-stabilized nickel ferrocyanide nanoparticles for supercapacitor applications†

IF 4.7 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Pooja Kumari, Lungelo Lekokotla, Chandan Saha, Sarit K Ghosh, Harishchandra Singh and Kaushik Mallick
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Abstract

Supercapacitors are gaining attention as an ideal energy storage solution due to their excellent specific power, fast charging rates and high durability. This study presents the development of an organic molecule stabilized nickel ferrocyanide (NFC) hybrid material, synthesized through a complexation-mediated approach, which demonstrates outstanding electrochemical performance, making it a promising candidate for high-efficiency supercapacitor applications. X-ray diffraction analysis confirms the formation of nickel ferrocyanide with a cubic crystal structure (space group: Fmm). Transmission electron microscopy analysis revealed spherical shaped nickel ferrocyanide particles within the size range of 2–4 nm. Fourier-transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy confirmed the successful formation of nickel ferrocyanide and offered detailed insights into its bonding environment and chemical states. The electrochemical performance of the hybrid material displayed a specific capacitance of 298 F g−1 at 6 A g−1 and retained 88% of its original capacitance after 10 000 cycles in a three-electrode system. An asymmetric supercapacitor device, fabricated using NFC as the cathode and activated carbon as the anode electrode, delivered a specific capacitance of 94 F g−1 at 1.0 A g−1. The device exhibited maximum specific energy and specific power values of 44 W h kg−1 and 6067 W kg−1, respectively, with a moderately good cycle life (84% capacitance retention after 10 000 cycles). The results emphasize the potential of the NFC-based hybrid system as an efficient material for energy storage applications.

Abstract Image

用于超级电容器的有机分子稳定亚铁氰化镍纳米颗粒储能性能研究
超级电容器因其优异的比功率、快速充电速率和高耐用性而成为一种理想的储能解决方案。本研究通过络合介导的方法合成了一种有机分子稳定的亚铁氰化镍(NFC)杂化材料,该材料具有出色的电化学性能,使其成为高效超级电容器应用的有希望的候选材料。x射线衍射分析证实形成了具有立方晶体结构(空间群:Fmm)的亚铁氰化镍。透射电镜分析显示,颗粒呈球形,尺寸在2 ~ 4nm之间。傅里叶变换红外光谱、拉曼光谱和x射线光电子能谱证实了亚铁氰化镍的成功形成,并提供了对其成键环境和化学状态的详细见解。复合材料在6 a g−1条件下的比电容为298 F g−1,在三电极系统中循环10000次后仍保持88%的原始电容。以NFC为阴极,活性炭为阳极制备的非对称超级电容器器件在1.0 a g−1时的比电容为94 F g−1。该器件的最大比能量和比功率值分别为44 W h kg - 1和6067 W kg - 1,具有较好的循环寿命(10,000次循环后电容保持率为84%)。研究结果强调了基于nfc的混合系统作为一种高效储能材料的潜力。
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来源期刊
Materials Advances
Materials Advances MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.60
自引率
2.00%
发文量
665
审稿时长
5 weeks
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