Exploring the potential of metal tailored imine based covalent organic framework for asymmetric supercapacitor applications

IF 4 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Structure Pub Date : 2024-09-13 DOI:10.1016/j.molstruc.2024.139983
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Abstract

Currently, a fascinating area of research involves the development of stable and efficient materials for energy storage systems. The current work describes the synthesis of imine linked covalent organic framework (COF) using 4,4′,4′',4′''-(ethene-1,1,2,2-tetrayl) tetraaniline and terephthalaldehyde (TAT-COF) as precursors through solvothermal method. In addition, cobalt has been integrated to the imine linkage of TAT-COF to generate CO@TAT-COF. The X-ray diffraction study reveals the formation of ordered and crystalline TAT-COF with eclipsed (AA) stacking configuration. Morphological characterization indicated the accumulation of metal species over stick like structured TAT-COF. Energy-dispersive X-ray (EDX) and Fourier Transform Infrared Spectroscopy results shows the successive intercalation of Co to the TAT-COF matrix. TAT-COF and Co@TAT-COF were examined towards electrochemical performance for supercapacitor applications. A two fold higher specific capacitance (Csp) was obtained in Co@TAT-COF (637 F/g) compared to TAT-COF (315 F/g) at 5 mV/s scan rate. The Co@TAT-COF showed an energy density (ED) of 58 Wh/kg at a power density of (PD) of 1500 W/kg. Enhanced electrochemical performance in Co@TAT-COF could be attributed to the structural confinement, conductivity, enhanced interlayer spacing and porosity. Co@TAT-COF has been used as positive electrode to fabricate an asymmetric device (ASD) in using Swagelok cell. The Csp of the fabricated ASD was found to be 95 F/g at 2 mV/s scan rate. ASD showed good stability with 73 % retention of Csp over 5000 charge/discharge cycles. The obtained results indicate the suitability of the engineered COFs towards energy storage devices.

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探索基于金属定制亚胺的共价有机框架在不对称超级电容器应用中的潜力
目前,一个引人入胜的研究领域是开发用于储能系统的稳定而高效的材料。本研究以 4,4′,4′',4′''-(乙烯-1,1,2,2-四基)四苯胺和对苯二甲醛(TAT-COF)为前体,通过溶热法合成了亚胺连接的共价有机框架(COF)。此外,钴与 TAT-COF 的亚胺连接生成 CO@TAT-COF。X 射线衍射研究显示,TAT-COF 形成了有序的结晶,并具有蚀刻(AA)堆积构型。形态表征表明,金属物种聚集在棒状结构的 TAT-COF 上。能量色散 X 射线(EDX)和傅立叶变换红外光谱分析结果表明,钴在 TAT-COF 基体中连续插层。对 TAT-COF 和 Co@TAT-COF 在超级电容器应用中的电化学性能进行了检验。在 5 mV/s 的扫描速率下,Co@TAT-COF(637 F/g)的比电容(Csp)比 TAT-COF(315 F/g)高出两倍。在功率密度(PD)为 1500 W/kg 时,Co@TAT-COF 的能量密度(ED)为 58 Wh/kg。Co@TAT-COF 中增强的电化学性能可归因于其结构限制、导电性、增强的层间间距和多孔性。Co@TAT-COF 被用作正电极,利用世伟洛克电池制造出了一个不对称器件(ASD)。在 2 mV/s 的扫描速率下,所制造的 ASD 的 Csp 为 95 F/g。ASD 显示出良好的稳定性,在 5000 次充电/放电循环中,Csp 保持率为 73%。这些结果表明,工程 COFs 适用于储能设备。
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来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
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