Naga Keerthana Apparla, Antara Vaidyanathan, Brahmananda Chakraborty, Chandra Shekhar Sharma
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引用次数: 0
摘要
活性炭具有高比表面积、大孔隙率和易于制备等特殊属性,因此在能量存储方面前景广阔。在这里,我们用低成本的蜡烛烟灰合成了活性炭,并将其用作超级电容器的电极。在以 1 M H2SO4 为电解质的三电极设置中,评估了活化蜡烛烟灰(ACS)和未活化蜡烛烟灰(CS)的电化学特性。在电流密度为 2 A g-1 时,ACS 和 CS 的比电容分别为 467 F g-1 和 180 F g-1。ACS 电化学性能的提高归因于活化后表面积的增加,而表面积的增加起到了容纳大量电解质离子的作用。此外,对 ACS 对称电池进行的双电极研究显示,在 1 A g-1 的条件下,其电容高达 397 F g-1。在 10 A g-1 的高电流密度下,ACS 系统在 10,000 次循环中保持了 82% 的电容。在 574.8 W kg-1 的比功率下,该系统的比能量为 19.8 Wh kg-1。我们进行了密度泛函理论(DFT)模拟来验证实验观察结果,发现 ACS 的量子电容大于 CS。此外,离子在 ACS 表面扩散的势垒能低于 CS,这表明活化后的迁移率有所提高。
Experimental and Theoretical Investigation of Porous Carbon Nanospheres for Supercapacitor Application
Activated carbon holds a promising avenue in the context of energy storage because of its special attributes like high surface area, large pore volume, and ease of preparation. Herein, we synthesized the activated carbon from low-cost candle soot and employed it as an electrode for supercapacitor application. Activation resulted in a high specific surface area of 1679 m2 g−1 The electrochemical properties of activated candle soot (ACS) and unactivated candle soot (CS) are evaluated in a three-electrode setup using 1 M H2SO4 as an electrolyte. ACS and CS exhibited specific capacitance of 467 and 180 F g−1 at a current density of 2 A g−1, respectively. The improved electrochemical performance of ACS is attributed to an increase in surface area upon activation, which acts as a reservoir to accommodate a large number of electrolyte ions. Furthermore, two-electrode studies of ACS symmetric cells revealed the extraordinary capacitance of 397 F g−1 at 1 A g−1. The ACS system retained a capacitance of 82% for 10,000 cycles at a high current density of 10 A g−1. This system exhibited a specific energy of 19.8 Wh kg−1 at a specific power of 574.8 W kg−1. We performed density functional theory (DFT) simulations to validate the experimental observations and found that the quantum capacitance of ACS is greater than that of CS. Furthermore, the barrier energy for ionic diffusion across the surface of ACS is lower than that of CS, indicating improved mobility upon activation.