质子交换膜燃料电池
膜
材料科学
制作
化学工程
相对湿度
膜电极组件
涂层
极化(电化学)
传质
催化作用
图层(电子)
墨水池
热扩散率
浓差极化
气体扩散
氢
基质(水族馆)
工作温度
复合材料
电阻式触摸屏
电化学
分析化学(期刊)
扩散
扩散层
作者
Mohamed Zekri,Rolando Pedicini,Ada Saccà,Assunta Patti,Roberto D’Agostino,Flavio Librizzi,Alessandra Carbonea,Vincenzo Baglio,Irene Gatto
标识
DOI:10.1016/j.electacta.2026.148519
摘要
This study compares the electrochemical performance of proton exchange membrane fuel cells (PEMFCs) to analyze two innovative membrane-electrode assembly (MEA) fabrication processes: the spray catalyst-coated membrane (s-CCM) and the decal catalyst-coated membrane (d-CCM). In the s-CCM procedure, the catalyst ink is applied directly onto the membrane surface by spray coating procedure, followed by drying and hot pressing with the GDLs. In the d-CCM process, the catalyst ink is first deposited onto a PTFE substrate, which is then hot-pressed onto the membrane (decal); the PTFE substrate is subsequently removed, leaving the catalyst layer transferred to the membrane. Gas diffusion layers (GDLs) are then applied during final assembly. Polarization curves were recorded under various operating conditions, including temperatures ranging from 80 to 95 °C, relative humidity between 50% and 100%, and pressure from 1.5 to 3 bar, using hydrogen and air as reactant and oxidant gases, respectively. Under all test conditions, the d-CCM-MEA outperformed the s-CCM-MEA in terms of maximum power density, achieving a peak value of 1069 mW cm⁻² at 80 °C, 100% relative humidity, and 3 bar—approximately 65% higher than the s-CCM-MEA under the same operating conditions. This performance improvement is attributed to better catalyst–membrane interfacial contact, improved layer uniformity, and reduced mass transport resistance provided by the decal transfer process. These results highlight the significant influence of MEA fabrication on PEMFC performance and efficiency during operation.
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