Construction of a uniform zeolitic imidazole framework (ZIF-8) nanocrystal through a wet chemical route towards supercapacitor application

纳米晶 超级电容器 咪唑 材料科学 纳米技术 化学工程 化学 电化学 有机化学 电极 物理化学 工程类
作者
Iqra Rabani,Jewon Lee,Taeyoon Lim,Hai Bang Truong,Sobia Nisar,Sitara Afzal,Young‐Soo Seo
出处
期刊:RSC Advances [Royal Society of Chemistry]
卷期号:14 (1): 118-130 被引量:29
标识
DOI:10.1039/d3ra06941a
摘要

Exploring larger surface area electrode materials is crucial for the development of an efficient supercapacitors (SCs) with superior electrochemical performance. Herein, a cost-effective strategy was adopted to synthesize a series of ZIF8 nanocrystals, and their size effect as a function of surface area was also examined. The resultant ZIF8-4 nanocrystal exhibits a uniform hexagonal structure with a large surface area (2800 m2 g-1) and nanometre size while maintaining a yield as high as 78%. The SCs performance was explored by employing different aqueous electrolytes (0.5 M H2SO4 and 1 M KOH) in a three-electrode set-up. The SC performance using a basic electrolyte (1 M KOH) was superior owing to the high ionic mobility of K+. The optimized ZIF8-4 nanocrystal electrode showed a faradaic reaction with a highest capacitance of 1420 F g-1 at 1 A g-1 of current density compared to other as-prepared electrodes in the three-electrode assembly. In addition, the resultant ZIF8-4 was embedded into a symmetric supercapacitor (SSC), and the device offered 350 F g-1 of capacitance with a maximum energy and power density of 43.7 W h kg-1 and 900 W kg-1 at 1 A g-1 of current density, respectively. To determine the practical viewpoint and real-world applications of the ZIF8-4 SSC device, 7000 GCD cycles were performed at 10 A g-1 of current density. Significantly, the device exhibited a cycling stability around 90% compared to the initial capacitance. Therefore, these findings provide a pathway for constructing large surface area ZIF8-based electrodes for high-value-added energy storage applications, particularly supercapacitors.
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
zyf发布了新的文献求助10
1秒前
2秒前
佳简成初发布了新的文献求助30
3秒前
鸭鸭完成签到,获得积分10
4秒前
Hello应助不羁采纳,获得10
4秒前
大模型应助温暖元容采纳,获得10
5秒前
justlmq完成签到,获得积分10
5秒前
林昊发布了新的文献求助10
5秒前
5秒前
7秒前
7秒前
10秒前
NexusExplorer应助Strix采纳,获得10
10秒前
chao发布了新的文献求助10
12秒前
Xuech发布了新的文献求助10
12秒前
you完成签到,获得积分10
14秒前
热心的血茗完成签到,获得积分10
14秒前
Polidori发布了新的文献求助10
16秒前
hhhh完成签到,获得积分10
17秒前
华仔应助Joyi采纳,获得10
19秒前
小朱完成签到 ,获得积分10
19秒前
Jasper应助林昊采纳,获得30
19秒前
20秒前
20秒前
20秒前
爱听歌纸飞机完成签到,获得积分10
21秒前
李健应助Yutong采纳,获得30
22秒前
dry发布了新的文献求助10
23秒前
23秒前
23秒前
科研通AI6.2应助zuo20050727采纳,获得10
25秒前
25秒前
chao完成签到,获得积分10
25秒前
26秒前
vince完成签到 ,获得积分10
27秒前
yygz0703完成签到,获得积分10
28秒前
华仔应助鸣丘采纳,获得10
28秒前
LittleTT发布了新的文献求助10
28秒前
28秒前
29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 7631703
求助须知:如何正确求助?哪些是违规求助? 9206168
关于积分的说明 19743538
捐赠科研通 7200887
什么是DOI,文献DOI怎么找? 3274664
关于科研通互助平台的介绍 2436554
邀请新用户注册赠送积分活动 2271265