催化作用
化学工程
材料科学
燃料电池
铂金
介孔材料
堆栈(抽象数据类型)
多孔性
相对湿度
化学计量学
质子交换膜燃料电池
电流密度
膜
膜电极组件
纳米技术
毛细管作用
选择性
交换电流密度
电催化剂
纳米颗粒
介孔二氧化硅
作者
Lixiao Shen,Y. F. Zhang,Miao Ma,Peiyuan Shao,Zigang Zhao,Wen Ye,Hongye Hu,S. J. Lin,Maolin Du,Y. Wang,Yunkun Dai,Pan Guo,Bo Liu,Bing Liu,Ziyu Zhang,Xulei Sui,L. Zhao,Z. H. Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-12-22
卷期号:16 (2): 1433-1446
被引量:1
标识
DOI:10.1021/acscatal.5c07476
摘要
Proton exchange membrane fuel cells (PEMFCs) are increasingly shifting toward low-humidity operation to simplify systems and improve efficiency, necessitating advanced electrocatalyst designs. Herein, we present a mesopore-confined platinum (Pt) catalyst with a high Pt site density that effectively addresses key challenges under dry conditions. The abundant mesopores enhance water retention via capillary condensation, while the high Pt density shortens the nearest-neighbor distance, maintaining continuous proton pathways under low humidity. Additionally, mesopore confinement suppresses Ostwald ripening, significantly enhancing durability. In single-cell tests under H2/air (0.5/2 L min–1, 150 kPa back pressure), the mesoporous carbon-based MEA (m-MEA) achieved 0.719 V at 2000 mA cm–2, exceeding the porous carbon-based MEA (p-MEA) by 58 mV. In a liquid-cooled stack (H2/air, stoichiometry 1.8/2, 50% relative humidity (RH), 150 kPa back pressure), it reached 0.700 V at 2000 mA cm–2, with a 64 mV improvement. Under fan-forced air and ambient pressure, the m-MEA maintained 0.732 V at 500 mA cm–2, surpassing the p-MEA by 81 mV. After 30,000 accelerated stress test (AST) cycles, the m-MEA showed only 26 mV decay at 800 mA cm–2, 61.7% lower than the p-MEA’s 68 mV decay, meeting DOE 2025 target of 30 mV.
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