提高pecvd制备的MWCNTs的电化学性能:电解质选择对电化学特性和器件功能的影响

IF 4.3 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Nitin Kumar Gautam , Nagih M. Shaalan , Saurabh Dalela , P.A. Alvi , Faheem Ahmed , Ranjeet Kumar Brajpuriya , Kavita Kumari , B.H. Koo , Aditya Sharma , Shalendra Kumar
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引用次数: 0

摘要

本研究探讨了电解质对PE-CVD合成的MWCNTs的影响,旨在通过比较电化学研究来弥补在选择最适合MWCNTs超级电容器电极的电解质方面的关键知识空白。采用x射线衍射(XRD)、拉曼光谱(Raman spectroscopy)和高分辨率透射电子显微镜(HR-TEM)对其进行了结构分析。XRD谱图中2θ ~ 25.40°处的反射,以及Raman光谱中1324 cm−1和1576 cm−1处的两个强波段证实了MWCNTs的单相性质。FE-SEM图像显示出致密的管状纳米结构。~ 0.348 nm的面间距进一步验证了MWCNTs的成功生长。MWCNTs具有较高的吸附能力,其比表面积(SSA)为68.73 m2/g,平均孔径为44.12 Å。采用电化学阻抗谱法(EIS)、恒流充放电法(GCD)和循环伏安法(CV)评价了1 M KCl、KOH、Na2SO4和NaOH电解质溶液中的电化学特性。GCD分析显示,MWCNTs在1 M NaOH中表现出最高的比电容,在1 A/g时为65.23 F/g。CV分析表明,在1 M KCl、KOH、Na2SO4和NaOH电解液中,扫描速率为5 mV/s时,比电容分别为61.51、67.38、71.63和72.17 F/g。根据循环稳定性研究,电极在1 M NaOH中循环1000次仍保持高度稳定,保留率为98%。此外,使用MWCNTs设计的对称超级电容器器件在GCD (0.25 a /g电流密度)和CV (5 mV/s扫描速率)下的比电容分别为26.75 F/g和23.57 F/g。观察到的能量和功率密度分别为3.71 Wh/Kg和5000 W/ Kg,在1000次循环后保留率为89%,表明其在未来储能应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing electrochemical performance of PECVD-fabricated MWCNTs: Influence of electrolyte selection on electrochemical traits and device functionality
This study investigates the impact of electrolytes on MWCNTs synthesized through PE-CVD, aiming to bridge the critical knowledge gap in selecting the most suitable electrolyte for MWCNT-based supercapacitor electrodes by performing a comparative electrochemical study. The structural analysis was carried out using X-ray diffraction (XRD), Raman spectroscopy, and high-resolution transmission electron microscopy (HR-TEM). The reflection at 2θ ∼25.40° in the XRD pattern, while two intense bands at 1324 cm−1 and 1576 cm−1 in Raman spectroscopy confirm the single-phase nature of MWCNTs. The FE-SEM image demonstrates dense tubular-type nanostructures. The interplanar spacing of ∼0.348 nm further validates the successful growth of MWCNTs. The MWCNTs had a high adsorption capacity with a specific surface area (SSA) of 68.73 m2/g and a 44.12 Å of average pore size. Electrochemical impedance spectroscopy (EIS), galvanostatic charge-discharge (GCD), and cyclic voltammetry (CV) were used to evaluate the electrochemical characteristics in 1 M KCl, KOH, Na2SO4, and NaOH electrolyte solutions. The GCD analysis revealed that the MWCNTs exhibited the highest specific capacitance in 1 M NaOH, which was 65.23 F/g at 1 A/g. In addition, the CV analysis indicated the specific capacitance of 61.51, 67.38, 71.63, and 72.17 F/g at a scan rate of 5 mV/s in 1 M KCl, KOH, Na2SO4, and NaOH electrolytes, respectively. According to the cyclic stability studies, the electrodes remained highly stable over 1000 cycles in 1 M NaOH, which shows 98 % retention. Furthermore, a symmetric supercapacitor device designed using MWCNTs exhibited a specific capacitance of 26.75 F/g and 23.57 F/g from GCD (0.25 A/g current density) and CV (5 mV/s scan rate), respectively. The observed energy and power densities were 3.71 Wh/Kg and 5000 W/kg, respectively, with a retention of 89 % after 1000 cycles, indicating its potential for future energy storage applications.
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来源期刊
Journal of Physics and Chemistry of Solids
Journal of Physics and Chemistry of Solids 工程技术-化学综合
CiteScore
7.80
自引率
2.50%
发文量
605
审稿时长
40 days
期刊介绍: The Journal of Physics and Chemistry of Solids is a well-established international medium for publication of archival research in condensed matter and materials sciences. Areas of interest broadly include experimental and theoretical research on electronic, magnetic, spectroscopic and structural properties as well as the statistical mechanics and thermodynamics of materials. The focus is on gaining physical and chemical insight into the properties and potential applications of condensed matter systems. Within the broad scope of the journal, beyond regular contributions, the editors have identified submissions in the following areas of physics and chemistry of solids to be of special current interest to the journal: Low-dimensional systems Exotic states of quantum electron matter including topological phases Energy conversion and storage Interfaces, nanoparticles and catalysts.
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