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
刚刚
Omg发布了新的文献求助10
1秒前
1秒前
2秒前
2秒前
科研通AI6.4应助naya6600采纳,获得10
3秒前
4秒前
future完成签到,获得积分10
5秒前
娇娇大王发布了新的文献求助10
5秒前
脑洞疼应助ssmffryjj888采纳,获得10
6秒前
MrG完成签到,获得积分10
6秒前
guanqi完成签到 ,获得积分10
6秒前
小液滴发布了新的文献求助10
7秒前
肥龙宝宝发布了新的文献求助10
7秒前
faye完成签到,获得积分10
8秒前
8秒前
完美世界应助Eric_Zhou采纳,获得10
8秒前
真难啊完成签到 ,获得积分10
8秒前
8秒前
田様应助Omg采纳,获得10
14秒前
经竺完成签到,获得积分10
14秒前
桐桐应助魔幻的可乐采纳,获得10
15秒前
15秒前
15秒前
ZJK发布了新的文献求助10
16秒前
Yallabo完成签到,获得积分10
17秒前
lfydhk发布了新的文献求助10
17秒前
深情的访彤完成签到,获得积分20
17秒前
Essence完成签到,获得积分10
18秒前
18秒前
阿晚发布了新的文献求助10
20秒前
李梦媛完成签到,获得积分10
21秒前
21秒前
搜集达人应助肥龙宝宝采纳,获得10
22秒前
PATTOM完成签到,获得积分10
22秒前
充电宝应助lllll采纳,获得10
23秒前
谦让的牛排完成签到 ,获得积分10
24秒前
体贴琳完成签到 ,获得积分10
25秒前
25秒前
25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
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
煤炭地下气化渗流燃烧方法的研究 400
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 7632347
求助须知:如何正确求助?哪些是违规求助? 9206786
关于积分的说明 19745657
捐赠科研通 7201732
什么是DOI,文献DOI怎么找? 3274805
关于科研通互助平台的介绍 2436711
邀请新用户注册赠送积分活动 2271485