基于绿色合成氧化镍纳米粒子和石墨烯的对称和不对称超级电容器制造

IF 1.4 4区 化学 Q4 CHEMISTRY, PHYSICAL Colloid Journal Pub Date : 2024-04-10 DOI:10.1134/S1061933X23600914
A. Zemieche, L. Chetibi, D. Hamana, S. Achour, V. D. Noto
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引用次数: 0

摘要

摘要 利用含有一系列多酚的橄榄叶提取物(OLE)合成了氧化镍纳米粒子(NiO NPs)。这些多酚既是还原剂,又是封盖剂,可稳定纳米粒子。醋酸镍水溶液被用作前体。同时,在水溶液中通过电化学剥离石墨获得剥离石墨烯(EG)。这些材料被用作超级电容器应用中的电活性成分。对氧化镍和石墨烯的表征包括热重分析 (TGA)、X 射线衍射 (XRD)、拉曼光谱 (RS)、X 射线光电子能谱 (XPS)、扫描/透射电子显微镜 (SEM/TEM),以及布鲁瑙尔-艾美特-泰勒 (BET) 分析。显微照片显示,NiO 和 EG 都具有纳米级的尺寸和相当大的表面积,BET 分析也证实了这一点。采用刮刀法制造了对称(NiO/NiO、EG/EG)和不对称(NiO/EG)超级电容器。利用场发射扫描电子显微镜(FESEM)、循环伏安法(CV)和电化学阻抗谱(EIS)对电极进行了评估,结果表明电极具有良好的形态和电化学特性。在低扫描速率下,对称和非对称超级电容器都表现出显著的重力电容(1 mV s-1 时分别为 221、111 和 162 F g-1)。此外,它们还显示出更高的功率密度(10 mV s-1 时分别为 173、137 和 161 W kg-1),分别展示了 NiO NPs 和 EG 的伪电容和双电层电容器 (EDLC) 行为。这项研究提出了一种可持续的氧化镍氮氧化物合成路线,开发了高性能超级电容器电极,并实现了对氧化镍氮氧化物和 EG 电化学行为的全面了解,因而具有重要价值。
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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Symmetric and Asymmetric Supercapacitor Fabrication Based on Green Synthesized NiO Nanoparticles and Graphene

Nickel oxide nanoparticles (NiO NPs) are synthesized using olive leaf extract (OLE), which contains a range of polyphenols. These polyphenols serve as both reducing and capping agents, stabilizing the nanoparticles. Aqueous nickel acetate is employed as a precursor. Simultaneously, exfoliated graphene (EG) is obtained via electrochemical exfoliation of graphite in aqueous solutions. These materials were employed as electroactive components in supercapacitor applications. Characterization of NiO and EG involved thermogravimetric analysis (TGA), X-ray diffraction (XRD), Raman spectroscopy (RS), X-ray photoelectron spectroscopy (XPS), and scanning/transmission electron microscopy (SEM/TEM), alongside Brunauer−Emmett−Teller (BET) analysis, confirming the formation of crystalline NiO NPs with a cubic phase and Fm-3m space group. Micrographs revealed nanoscale dimensions for both NiO and EG with a substantial surface area, as verified by BET analysis. Symmetric (NiO/NiO, EG/EG) and asymmetric (NiO/EG) supercapacitors were fabricated using the doctor blade method. Electrode evaluation, employing field-emission scanning electron microscopy FESEM, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS), demonstrated promising morphological and electrochemical characteristics. At low scan rates, both symmetric and asymmetric supercapacitors exhibited a notable gravimetric capacitance (221, 111, and 162 F g–1 at 1 mV s–1). Additionally, they revealed higher power density (173, 137, and 161 W kg–1 at 10 mV s–1), showcasing pseudocapacitive and electric double-layer capacitor (EDLC) behavior for NiO NPs and EG, respectively. This research significantly contributes valuable insights by presenting a sustainable synthesis route for NiO NPs, developing high-performance supercapacitor electrodes, and achieving a comprehensive understanding of the electrochemical behavior of NiO NPs and EG.

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来源期刊
Colloid Journal
Colloid Journal 化学-物理化学
CiteScore
2.20
自引率
18.20%
发文量
36
审稿时长
6-12 weeks
期刊介绍: Colloid Journal (Kolloidnyi Zhurnal) is the only journal in Russia that publishes the results of research in the area of chemical science dealing with the disperse state of matter and surface phenomena in disperse systems. The journal covers experimental and theoretical works on a great variety of colloid and surface phenomena: the structure and properties of interfaces; adsorption phenomena and structure of adsorption layers of surfactants; capillary phenomena; wetting films; wetting and spreading; and detergency. The formation of colloid systems, their molecular-kinetic and optical properties, surface forces, interaction of colloidal particles, stabilization, and criteria of stability loss of different disperse systems (lyosols and aerosols, suspensions, emulsions, foams, and micellar systems) are also topics of the journal. Colloid Journal also includes the phenomena of electro- and diffusiophoresis, electro- and thermoosmosis, and capillary and reverse osmosis, i.e., phenomena dealing with the existence of diffusion layers of molecules and ions in the vicinity of the interface.
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