Freestanding Carbon Nanofibers Derived from Biopolymer (Kraft Lignin) as Ultra-Microporous Electrodes for Supercapacitors

IF 4.6 4区 化学 Q2 ELECTROCHEMISTRY
Batteries Pub Date : 2023-11-24 DOI:10.3390/batteries9120566
Y. J. Dias, Vinícius D. Silva, B. Pourdeyhimi, Eliton S. Medeiros, Alexander L. Yarin
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Abstract

Lignin-derived carbon nanofibers (LCNFs) formed via the solution blowing of a biopolymer are developed here as a promising replacement for polyacrylonitrile (PAN)-derived carbon nanofibers (PCNFs) formed via electrospinning for such applications as supercapacitor (SC) electrodes. Accordingly, it is demonstrated here that a biopolymer (kraft lignin, which is, essentially, a waste material) can substitute a petroleum-derived polymer (PAN). Moreover, this can be achieved using a much faster and safer fiber-forming method. The present work employs the solution blowing of lignin-derived nonwovens and their carbonization to form electrode materials. These materials are characterized and explored as the electrodes in supercapacitor prototypes. Given the porosity importance of carbon fibers in SC applications, N2 gas adsorption tests were performed for characterization. LCNFs revealed the specific surface area (SSA) and capacitance values as high as 1726 m2/g and 11.95 F/g, which are about one-half of those for PCNFs, 3624 m2/g and 25.5 F/g, respectively. The capacitance values of LCNFs are comparable with those reported in the literature, but the SSA observed here is much higher. Moreover, no further post-carbonization activation steps were performed here in comparison with those materials reported in the literature. It was also found here that fiber pre-oxidation in air prior to carbonization and the addition of zinc chloride affect the SSA and capacitance values of both LCNFs and PCNFs. The electrochemical tests of the SCs prototypes were used to evaluate their capacitance at different charging rates, voltage windows, and the number of cycles. The capacitance of PCNFs decreased by about 47% during fast charging, while the capacitance of LCNFs improved during fast charging, bringing them to the level of only 21% below that of PCNFs. These changes were correlated with the packing density of the electrodes. It should be emphasized that LCNFs revealed a much higher mass yield, which was 4–5 times higher than that of PCNFs. LCNFs also possess a higher packing density, a lower price, and cause a significantly lower environmental impact than PCNFs. The best cell supercapacitor delivered a maximum specific energy of 1.77 Wh/kg and a maximum specific power of 156 kW/kg, surpassing conventional electrochemical supercapacitors. Remarkably, it retained 95.2% of its initial capacitance after 10,000 GCD cycles at a current density of 0.25 A/g, indicating robust stability. Accordingly, kraft lignin, a bio-waste material, holds great promise as a raw material for supercapacitor electrodes.
由生物聚合物(牛皮纸木质素)衍生的独立碳纳米纤维作为超级电容器的超微孔电极
本文开发的木质素衍生碳纳米纤维(LCNFs)是通过生物聚合物溶液发泡形成的,有望替代通过电纺丝形成的聚丙烯腈(PAN)衍生碳纳米纤维(PCNFs),用于超级电容器(SC)电极等应用。因此,本文证明生物聚合物(牛皮纸木质素,本质上是一种废料)可以替代石油衍生聚合物(PAN)。此外,还可以使用更快、更安全的纤维成型方法来实现这一目标。本研究采用溶液吹制木质素衍生非织造布,并对其进行碳化处理,以形成电极材料。对这些材料进行了表征,并探讨了在超级电容器原型中用作电极的可能性。鉴于碳纤维的多孔性在 SC 应用中的重要性,对其进行了 N2 气体吸附测试,以确定其特性。LCNFs 的比表面积 (SSA) 和电容值分别高达 1726 m2/g 和 11.95 F/g,约为 PCNFs(3624 m2/g 和 25.5 F/g)的二分之一。LCNFs 的电容值与文献报道的电容值相当,但这里观察到的 SSA 要高得多。此外,与文献中报道的材料相比,这里没有进行进一步的碳化后活化步骤。研究还发现,碳化前纤维在空气中的预氧化以及氯化锌的添加会影响 LCNF 和 PCNF 的 SSA 和电容值。SCs 原型的电化学测试用于评估它们在不同充电速率、电压窗口和循环次数下的电容。在快速充电过程中,PCNFs 的电容降低了约 47%,而 LCNFs 的电容在快速充电过程中有所提高,仅比 PCNFs 低 21%。这些变化与电极的堆积密度有关。需要强调的是,LCNFs 的质量产量要高得多,是 PCNFs 的 4-5 倍。与 PCNF 相比,LCNF 的堆积密度更高,价格更低,对环境的影响也更小。最佳电池超级电容器的最大比能量为 1.77 Wh/kg,最大比功率为 156 kW/kg,超过了传统的电化学超级电容器。值得注意的是,在电流密度为 0.25 A/g 的条件下,经过 10,000 次 GCD 循环后,它仍能保持 95.2% 的初始电容,这表明它具有很强的稳定性。因此,牛皮纸木质素这种生物废料有望成为超级电容器电极的原材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Batteries
Batteries Energy-Energy Engineering and Power Technology
CiteScore
4.00
自引率
15.00%
发文量
217
审稿时长
7 weeks
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