Niobium doped triazine based covalent organic frameworks for supercapacitor applications

超级电容器 三嗪 兴奋剂 共价有机骨架 水平扫描速率 共价键 纳米技术 材料科学 化学工程 电化学 多孔性 化学 循环伏安法 复合材料 光电子学 有机化学 冶金 电容 高分子化学 电极 物理化学 工程类
作者
H. Shanavaz,B.P. Prasanna,S. Archana,M.K. Prashanth,Fahad A. Alharthi,Rui Zhou,M.S. Raghu,Byong‐Hun Jeon,K. Yogesh Kumar
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:67: 107561-107561 被引量:47
标识
DOI:10.1016/j.est.2023.107561
摘要

Covalent organic frameworks (COFs) are gaining high importance in energy storage systems due to their uniform porosity and versatile functionality. The present work deals with the fabrication of triazine-based COF through Schiff base formation. The method involves the polycondensation reaction between melamine and terephthalaldehyde. In addition, the COF was also decorated with Niobium to generate Nb@COF. The morphological, elemental mapping, X-ray photoelectron spectroscopy, C13 NMR results show the effective doping of Nb to the COF and provide insights into the nature of bond formation. The obtained experimental XRD results are in good agreement with Materials Studio simulated results. COF and Nb@COF have been used for supercapacitor applications in a three-electrode system. Enhanced specific capacitance was observed in Nb@COF (367 F g−1) compared to pure COF (244 F g−1) at a scan rate of 2 mV s−1. The superior electrochemical performance in Nb@COF could be due to the increased porosity and interlayer spacing. COF and Nb@COF exhibited good stability towards charge and discharge and managed to retain 82 and 89 % specific capacitance, respectively even at 5000 cycles. COF and Nb@COF were assembled in a coin cell and fabricated an asymmetric supercapacitor device as negative and positive electrodes, respectively. The results obtained were satisfactory and shows a specific capacitance of 87 F g−1 at a scan rate of 2 mV s−1.The good stability, specific capacitance and reliability of Nb@COF indicate its potential application in energy storage devices.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
毗昙发布了新的文献求助10
1秒前
王君青见完成签到,获得积分10
1秒前
搜集达人应助晶晶采纳,获得10
1秒前
Owen应助怕黑的寻菱采纳,获得10
1秒前
wjx发布了新的文献求助10
2秒前
S僊完成签到,获得积分10
2秒前
2秒前
慕青应助yhz96采纳,获得10
3秒前
露桥闻笛发布了新的文献求助30
3秒前
3秒前
赘婿应助huwenbin采纳,获得10
3秒前
4秒前
英姑应助龙傲天采纳,获得10
4秒前
4秒前
传奇3应助甜甜凌青采纳,获得10
4秒前
在水一方应助舒心冷珍采纳,获得10
4秒前
大模型应助优美安梦采纳,获得10
5秒前
黄诗淇发布了新的文献求助10
5秒前
五积散发布了新的文献求助10
5秒前
Twinkle完成签到,获得积分10
6秒前
guli完成签到,获得积分20
6秒前
sagitar应助immm采纳,获得20
7秒前
顽石发布了新的文献求助10
7秒前
wz完成签到,获得积分10
7秒前
7秒前
8秒前
8秒前
8秒前
8秒前
谁是mxh完成签到,获得积分20
8秒前
12366666发布了新的文献求助20
8秒前
8秒前
8秒前
S僊发布了新的文献求助10
8秒前
9秒前
9秒前
9秒前
9秒前
权幻珊发布了新的文献求助10
9秒前
suye关注了科研通微信公众号
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Principles of town planning: translating concepts to applications 1000
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The Effective Clinical Neurologist 3ed 500
The Great Hymn to Šamaš 500
Positive Obsession: The Life and Times of Octavia E. Butler 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7697370
求助须知:如何正确求助?哪些是违规求助? 9257430
关于积分的说明 20008315
捐赠科研通 7271979
什么是DOI,文献DOI怎么找? 3293080
关于科研通互助平台的介绍 2448568
邀请新用户注册赠送积分活动 2298972