Monitoring Carbon Corrosion in Anode of a PEM Fuel Cells Under Fuel Starvation Using a Hydrogen Reference Electrode and on-Line Mass Spectrometry

聚合物电解质膜电解 阳极 质子交换膜燃料电池 电解 碳纤维 电解水 化学 腐蚀 直接乙醇燃料电池 化学工程 材料科学 电解质 催化作用 电极 复合材料 有机化学 物理化学 复合数 工程类
作者
Sunjin Park,Katie Heeyum Lim,Woong Hee Lee,Yoonjae Jeong,Hansung Kim
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2020-02 (33): 2115-2115
标识
DOI:10.1149/ma2020-02332115mtgabs
摘要

Polymer electrolyte membrane fuel cells (PEMFCs) has attracted great attention in transportation and stationary applications with zero emissions and high efficiency compared to conventional combustion engines. However, various factors limit the lifespan of PEMFCs, which remain a major obstacle to large-scale commercialization. In particular, corrosion of the carbon support is one of the main causes of fatal and irreversible deterioration of PEMFCs performance. If the hydrogen fuel supply is insufficient to maintain current demand due to poor water management or fuel depletion at the anode, carbon corrosion may occur on the anode side. In this fuel starvation condition, reactions that take place in place of hydrogen oxidation, such as water electrolysis and oxidation of the carbon support, compensate for the current shortage. The exact deterioration mechanism of PEMFCs in fuel starvation is investigated by simultaneously monitoring the potential behavior from the anode and the exhaust gas using hydrogen reference electrodes and in situ online mass spectrometry. Interestingly, water electrolysis starts at a lower potential range and carbon oxidation occurs at a higher range as an alternative reaction to hydrogen oxidation. Thus, carbon corrosion, which is detrimental to cell performance, can be reduced by extending the duration of the water electrolysis reaction. In this regard, the introductions of the graphitized carbon support and water electrolysis catalyst to the anode are effective in alleviating damage due to fuel starvation by making a dominant alternative reaction to continue electrolysis of water. And this alternative reaction is Monitored with a hydrogen reference electrode and using on-site online mass spectrometry.

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
科研通AI6.2应助jiangxiaoxu采纳,获得10
刚刚
在水一方应助jiangxiaoxu采纳,获得10
1秒前
科研通AI6.2应助huohuo采纳,获得10
1秒前
anan发布了新的文献求助10
1秒前
在水一方应助傅劲哲采纳,获得30
1秒前
领导范儿应助jiangxiaoxu采纳,获得10
1秒前
小马甲应助jiangxiaoxu采纳,获得10
1秒前
情怀应助jiangxiaoxu采纳,获得10
1秒前
2秒前
酷波er应助笨笨的毛豆采纳,获得10
2秒前
馨馨的科科应助历史真相采纳,获得10
2秒前
2秒前
科研通AI6.2应助细腻之云采纳,获得10
2秒前
小二郎应助精分的猫采纳,获得10
2秒前
2秒前
2秒前
科研通AI6.2应助idof采纳,获得10
3秒前
3秒前
优雅求知的桃子完成签到,获得积分10
3秒前
jiangxue完成签到,获得积分10
3秒前
SciGPT应助鳗鱼难破采纳,获得10
3秒前
Adream完成签到 ,获得积分10
4秒前
4秒前
molihuakai应助jason采纳,获得10
5秒前
传奇3应助萧平生采纳,获得10
5秒前
我是老大应助orad采纳,获得10
5秒前
单春栋发布了新的文献求助10
5秒前
zhtgang发布了新的文献求助10
5秒前
追寻的白昼完成签到 ,获得积分10
6秒前
激情的晓槐完成签到,获得积分10
6秒前
muziLi发布了新的文献求助10
7秒前
田睿完成签到,获得积分10
8秒前
8秒前
高高发布了新的文献求助10
8秒前
qkdxh完成签到,获得积分10
9秒前
阔达小松鼠完成签到,获得积分10
9秒前
9秒前
国服懒羊羊应助杨道之采纳,获得10
9秒前
国服懒羊羊应助杨道之采纳,获得10
10秒前
活泼的安南应助杨道之采纳,获得10
10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
Moody's Ratings Rising AI spending narrows the gap, but US hyperscalers retain edge over Chinese peers 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 7696376
求助须知:如何正确求助?哪些是违规求助? 9256483
关于积分的说明 20003111
捐赠科研通 7270732
什么是DOI,文献DOI怎么找? 3292730
关于科研通互助平台的介绍 2448354
邀请新用户注册赠送积分活动 2298412