催化作用
热解
酞菁
材料科学
碳纤维
纳米材料基催化剂
热分解
金属
吡啶
分解
无机化学
纳米颗粒
化学工程
热稳定性
热处理
氨
脱氢
贵金属
碳纳米管
可逆氢电极
化学
氰化物
电催化剂
脱羧
聚苯胺
质子交换膜燃料电池
除氧
作者
Ekaterina Pakrieva,Javier Hernández‐Ferrer,Gema Martı́nez,Francisco Balas,Enrique García‐Bordejé,Alejandro Ansón‐Casaos,Laura Simonelli,F. Bartolomé,Ana M. Benito,Wolfgang K. Maser,José L. Hueso,Jesús Santamaría
标识
DOI:10.1016/j.cej.2025.171198
摘要
The sluggish kinetics of the oxygen reduction reaction (ORR) remain a key bottleneck for the commercialization of proton exchange membrane fuel cells (PEMFCs), driving the search for efficient, non-precious metal catalysts. Herein, we present a laser-assisted pyrolysis strategy for the synthesis of nitrogen-doped carbon (NC) materials, both metal-free and containing atomically dispersed Fe and Co, using aerosolized phthalocyanine precursors and a near-instantaneous rapid decomposition under a high-energy laser beam, while preventing metal aggregation. A single-step post-synthetic thermal activation under an NH₃/N₂ atmosphere further tailors the textural and surface properties, without requiring ammonia co-feeding during laser pyrolysis, acid etching, or multiple treatments, marking a significant improvement over our previously reported single atom (Fe-N/C) protocols. The resulting Fe_Co/NC_tr catalyst exhibits high specific surface area, enhanced microporosity, improved graphitization, and increased abundance of electrochemically beneficial nitrogen sites. Compared to our earlier reported Fe–N/C catalysts, Fe_Co/NC_tr delivers significantly higher limiting current densities and enhanced durability in alkaline media. Overall, the developed Fe_Co/NC catalyst exhibits good ORR catalytic activity and outstanding long-term stability in alkaline media, comparable to the state-of-the-art commercial Pt/C catalysts. Cyanide poisoning tests confirm the essential role of atomically dispersed Fe 2+ and Co 2+ as active ORR sites.
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