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
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 H 2 /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 (H 2 /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.