电化学
合金
燃料电池
纳米颗粒
材料科学
氧还原
膜
化学工程
氧气
化学
质子交换膜燃料电池
氢
无机化学
电极
纳米技术
冶金
生物化学
有机化学
物理化学
工程类
作者
Maria V. Pagliaro,Lorenzo Poggini,Marco Bellini,L. Fei,Tailor Machado Peruzzolo,Hamish A. Miller
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2025-03-24
卷期号:15 (4): 306-306
标识
DOI:10.3390/catal15040306
摘要
Anion exchange membrane fuel cells (AEMFCs) are versatile power generation devices that can be fed by both gaseous (H2) and liquid fuels. The development of sustainable, efficient, and stable catalysts for the oxidation of hydrogen (HOR) and oxygen reduction (ORR) under alkaline conditions remains a challenge currently facing AEMFC technology. Reducing the loading of PGMs is essential for reducing the overall cost of AEMFCs. One strategy involves exploiting the synergistic effects of two metals in bimetallic nanoparticles (NPs). Here, we report that the activity for the HOR and the ORR can be finely tuned through surface engineering of carbon-supported PdAu-PVA NPs. The activity for both ORR and HOR can be adjusted by subjecting the material to heat treatment. Specifically, heat treatment at 500 °C under an inert atmosphere increases the crystallinity and oxophilicity of the nanoparticles, thereby enhancing anodic HOR performance. On the contrary, heat treatment significantly lowers ORR activity, highlighting how reduced surface oxophilicity plays a major role in increasing active sites for ORR. The tailored activity in these catalysts translates into high power densities when employed in AEMFCs (up to 1.1 W cm−2).
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