铂族
氧还原
燃料电池
氢
铂金
阴极
材料科学
氧还原反应
催化作用
化学
化学工程
电化学
电极
有机化学
工程类
物理化学
作者
Naomi Helsel,Pabitra Choudhury
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2025-06-13
卷期号:15 (6): 588-588
被引量:15
标识
DOI:10.3390/catal15060588
摘要
Although platinum-based catalysts are highly effective for the oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs), their high cost and scarcity limit large-scale commercialization. As a result, platinum group metal-free catalysts—particularly Fe-N-C materials—have received increasing attention as promising alternatives. Despite significant progress, no platinum-group metal-free (PGM-free) catalyst has yet matched the performance and durability of commercial Pt/C in acidic media. Recent advances in synthesis strategies, however, have led to notable improvements in the activity, stability, and active site density of Fe-N-C catalysts. This review highlights key synthesis approaches, including pyrolysis, MOF-derived templates, and cascade anchoring, and discusses how these methods contribute to improved nitrogen coordination, electronic structure modulation, and active site engineering. The continued refinement of these strategies, alongside improved catalyst screening techniques, is essential for closing the performance gap and enabling the practical deployment of non-PGM catalysts in PEMFC technologies.
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