材料科学
催化作用
质子交换膜燃料电池
电化学
铂金
炭黑
X射线光电子能谱
化学工程
碳纤维
密度泛函理论
纳米技术
碳纳米管
双功能
合理设计
表征(材料科学)
金属
纳米颗粒
结合能
铂纳米粒子
腐蚀
电化学能量转换
星团(航天器)
化学物理
电导率
过渡金属
燃料电池
作者
Yulia Bayan,E. R. Beskopylny,E. Yu. Gerasimov,Egor E. Aydakov,K.K. Volik,Ilya Pankov,Ilya V. Chepkasov,Mikhail M. Lukanov,Alexander G. Kvashnin,А. А. Алексеенко
出处
期刊:Small
[Wiley]
日期:2025-11-06
卷期号:21 (51): e10144-e10144
被引量:3
标识
DOI:10.1002/smll.202510144
摘要
Nitrogen-doped carbon supports enhance platinum electrocatalysts for proton exchange membrane fuel cells (PEMFCs). This study demonstrates a rapid melamine-assisted N-doping method for conductive carbon black (Ketjenblack EC600JD), producing a high-loading (≈40 wt.% Pt) catalyst with exceptional activity and durability. X-ray photoelectron spectroscopy confirms successful N-incorporation. Microscopy reveals uniform Pt nanoparticles (2.5-3 nm) and atomic Pt clusters on the N-doped support, attributed to strong Pt-N interactions. Density functional theory (DFT) calculations highlight the critical role of pyridinic-N defects in stabilizing atomic Pt, enhancing activity via charge transfer, and improving stability via strong Pt anchoring. Electrochemically, Pt/KB-600-N achieves twice the mass activity of commercial HiSPEC4000. After accelerated stress testing, it shows only a 15% electrochemical surface area (ESA) loss versus 35% for undoped Pt/KB-600. Enhanced stability correlates with pyridinic/graphitic N species mitigating carbon corrosion and Pt detachment. Binding energy analysis and cluster models quantify the Pt-support interaction, revealing N-doping increases Pt adhesion energy by 20-30% compared to pristine carbon. This work establishes a rational design strategy for high-performance Pt-based electrocatalysts by leveraging nitrogen-doped carbon supports, offering fundamental insights into the critical role of Pt-N interactions in enhancing both activity and durability for PEMFC applications.
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