Experimental investigation of degradation mechanism in proton exchange membrane water electrolyzer under prolonged and severe bubble accumulation condition

阳极 介电谱 塔菲尔方程 电解 材料科学 质子交换膜燃料电池 阴极 制氢 化学工程 扫描电子显微镜 能量色散X射线光谱学 聚合物电解质膜电解 分析化学(期刊) 电极 化学 电化学 电解质 复合材料 催化作用 物理化学 工程类 有机化学 生物化学 色谱法
作者
Haoran Zhou,Ben Chen,Kai Meng,Wenshang Chen,Guangfu Li,Zhengkai Tu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:491: 152202-152202 被引量:42
标识
DOI:10.1016/j.cej.2024.152202
摘要

Proton exchange membrane water electrolyzer (PEMWE) exhibits significant potential as a technology for hydrogen production driven by sustainable energy sources. In this study, the performance degradation characteristics of PEMWE under severe bubble accumulation condition lasting 100 h were investigated through in-situ and ex-situ characterization techniques. The results show that an increasing performance disparity with higher voltage, notably at lower temperatures, reaching a 58.2 % current density degradation rate at 50 °C and 2.0 V. Electrochemical impedance spectroscopy (EIS) analysis suggests that electrolyzer performance degradation is mainly due to increased charge transfer impedance, especially at the anode. In addition, the degraded electrolyzer exhibits a significant delay in reaching a stable current density during the abrupt voltage loading process, and its Tafel slope and electrochemically active surface area (ECSA) increased and decreased by 12.8 % and 13.5 %, respectively. Based on scanning electron microscopy (SEM) images, post-experiment analysis reveals pronounced thinning and noticeable cracks in both cathode and anode catalyst layers near the outlet, particularly on the anode side. Additionally, energy dispersive spectroscopy (EDS) mappings and transmission electron microscopy (TEM) images confirm substantial Pt/C and IrO2 catalyst particle dissolution, migration, and agglomeration. The findings of this study contribute to enhancing understanding of the performance degradation mechanisms in PEMWE.
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
Owen应助小猪采纳,获得10
1秒前
1秒前
2秒前
11完成签到,获得积分10
2秒前
2秒前
3秒前
了大憨发布了新的文献求助10
4秒前
体验发布了新的文献求助50
5秒前
11发布了新的文献求助10
5秒前
7秒前
科研通AI6.4应助张铁柱采纳,获得10
7秒前
HH发布了新的文献求助10
8秒前
YY再摆烂发布了新的文献求助10
8秒前
molihuakai应助友好寻真采纳,获得10
9秒前
李健应助xiaoyu采纳,获得10
9秒前
汉堡包应助科研通管家采纳,获得10
9秒前
Hello应助科研通管家采纳,获得10
10秒前
10秒前
慕青应助科研通管家采纳,获得10
10秒前
动听帆布鞋完成签到,获得积分10
10秒前
酷波er应助科研通管家采纳,获得10
10秒前
10秒前
英俊的铭应助科研通管家采纳,获得20
10秒前
无极微光应助科研通管家采纳,获得20
10秒前
科研通AI2S应助科研通管家采纳,获得10
10秒前
完美世界应助科研通管家采纳,获得10
10秒前
yjh123应助科研通管家采纳,获得10
10秒前
SciGPT应助科研通管家采纳,获得10
11秒前
11秒前
FashionBoy应助科研通管家采纳,获得10
11秒前
星辰大海应助科研通管家采纳,获得10
11秒前
phdbio应助shu采纳,获得30
11秒前
爆米花应助科研通管家采纳,获得10
11秒前
烟花应助科研通管家采纳,获得10
11秒前
斯文败类应助科研通管家采纳,获得10
11秒前
小蘑菇应助科研通管家采纳,获得10
11秒前
11秒前
科研通AI2S应助科研通管家采纳,获得10
11秒前
万能图书馆应助钱晓丹采纳,获得10
11秒前
HH完成签到,获得积分10
13秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Matrix Methods in Data Mining and Pattern Recognition 510
Reading and Understanding Health Research 500
Social Skills Improvement System-Rating Scales--Chinese Version 500
Dynamische Polarisation von H-1 und B-11 in (CH-3)-3NBH-3 500
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 7251301
求助须知:如何正确求助?哪些是违规求助? 8873881
关于积分的说明 18729674
捐赠科研通 6931011
什么是DOI,文献DOI怎么找? 3199343
关于科研通互助平台的介绍 2374325
邀请新用户注册赠送积分活动 2173988