An advanced large-porosity porous channel structure electrode for vanadium redox flow batteries

材料科学 电极 氧化还原 多孔性 化学工程 频道(广播) 复合材料 流动电池 电气工程 化学 电解质 冶金 工程类 物理化学
作者
Yifan Zhang,Xihao Zhang,Zeyu Xu,Denghua Zhang,Wenjie Yu,Yue Zhang,Lansong Liu,Jianguo Liu,Chuanwei Yan
出处
期刊:Journal of Power Sources [Elsevier BV]
卷期号:552: 232241-232241 被引量:33
标识
DOI:10.1016/j.jpowsour.2022.232241
摘要

Electrospinning technology has been extensively used to prepare electrodes for vanadium redox flow batteries (VRFBs). Nevertheless, electrospinning carbon nanofibers (ECNFs) electrodes suffer from low porosity and poor permeability, hence significantly hindering mass transport. To solve this critical issue, a new approach to prepare porous channel electrodes with large porosity based on electrospinning technology is proposed. The electrode is fabricated by electrospinning of polyacrylonitrile and poly (methyl methacrylate) (PMMA) solutions. PMMA not only acts as a sacrificial phase to form a porous channel structure inside the fibers, but also interconnects the fibers, which significantly increases the inter-fiber pore space and enhances the mass transfer performance. Electrochemical characterizations indicate that the electrodes have a remarkably elevated electrochemical specific surface area and outstanding electrochemical performance. Owing to the well-designed large-porosity porous channel structure of the electrode, the energy efficiency of the VRFB equipped with this electrode is 74.45% at 300 mA cm −2 and 81.03% at 200 mA cm −2 , and the battery can be continuously charged and discharged for more than 1200 cycles, which demonstrates a long-term cycling stability of the electrode. All of these indicate that this efficient and durable method for propagating electrode has broad application prospects. • Prepared an electrode with porous channel structure. • The electrodes exhibit enlarged pores while retaining large specific surface areas. • The design greatly improves activity of electrodes. • The prepared electrodes enable a significant enhancement in the battery performance.
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
kkny发布了新的文献求助10
1秒前
1秒前
2秒前
2秒前
loster完成签到,获得积分10
3秒前
张江泽完成签到,获得积分10
4秒前
seven完成签到,获得积分10
5秒前
5秒前
浏阳河发布了新的文献求助10
5秒前
Cres完成签到,获得积分10
7秒前
小短腿飞行员完成签到,获得积分10
7秒前
7秒前
8秒前
惠1发布了新的文献求助10
8秒前
端庄芯完成签到,获得积分10
9秒前
9秒前
1234567发布了新的文献求助10
9秒前
Lucas应助赵铁蛋采纳,获得10
10秒前
朴实小松鼠完成签到,获得积分10
11秒前
浏阳河完成签到,获得积分10
11秒前
小能完成签到,获得积分10
11秒前
11秒前
无极微光应助fangang采纳,获得50
11秒前
冷酷发布了新的文献求助10
12秒前
JASDLKJAJKCBN发布了新的文献求助10
13秒前
五颜六色的白完成签到,获得积分10
13秒前
14秒前
14秒前
14秒前
15秒前
思源应助Xinxxx采纳,获得10
15秒前
15秒前
烟花应助芭拉芭拉叭采纳,获得10
16秒前
宋鹏浩发布了新的文献求助10
16秒前
研友_VZG7GZ应助xyq采纳,获得10
17秒前
17秒前
Want完成签到,获得积分10
18秒前
18秒前
18秒前
Nexus应助cxcx采纳,获得10
18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
Developing Genetic Editing Tools for Lysobacter 2000
卤化钙钛矿人工突触的研究 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6520305
求助须知:如何正确求助?哪些是违规求助? 8313305
关于积分的说明 17780320
捐赠科研通 5622446
什么是DOI,文献DOI怎么找? 2927117
邀请新用户注册赠送积分活动 1903985
关于科研通互助平台的介绍 1764368