Anchoring ordered PtZn nanoparticles on MOF-derived carbon support for efficient oxygen reduction reaction in proton exchange membrane fuel cells

锚固 质子交换膜燃料电池 氧气 纳米颗粒 燃料电池 化学工程 碳纤维 氧还原反应 碳纳米颗粒 还原(数学) 氧还原 质子 化学 材料科学 纳米技术 有机化学 电化学 电极 复合材料 数学 物理化学 结构工程 复合数 工程类 生物化学 几何学 量子力学 物理
作者
KwangHo Lee,Eoyoon Lee,HyunWoo Chang,JeongHan Roh,SangJae Lee,Junu Bak,YongKeun Kwon,Hyung Chul Ham,EunAe Cho
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:505: 159350-159350 被引量:9
标识
DOI:10.1016/j.cej.2025.159350
摘要

• The ordered PtZn nanoparticles (O-PtZn) were synthesized on Zn and N-doped carbon (ZnNC). • The ZnNC support was utilized as a Zn source and an anchoring site. • The anchoring effect featured superior durability for oxygen reduction reaction in proton exchange membrane fuel cells. • Density functional theory calculation demonstrated the ZnNC has a strong binding energy with O-PtZn. Despite their superior catalytic activity for the oxygen reduction reaction (ORR), ordered platinum (Pt)-transition metal nanoparticles suffer from limitations that hinder their use in polymer electrolyte membrane fuel cells (PEMFCs), such as particle growth during the ordering transformation and insufficient durability over extended operation. In this study, a zeolitic imidazolate framework-8 (ZIF-8) is pyrolyzed into zinc and nitrogen-doped carbon (ZnNC). Pt nanoparticles are synthesized on the ZnNC and undergo heat treatment. Through this simple process, ordered PtZn nanoparticles are obtained with an average particle size of approximately 4.5 nm (O-PtZn/ZnNC). In a half-cell, the O-PtZn/ZnNC achieves outstanding ORR mass activity (1.21 A mg Pt −1 at 0.9 V) and durability (35 % loss of mass activity after 30 k cycles), significantly surpassing Pt/C (0.41 A mg Pt −1 and 61 % loss). As a cathode catalyst of a PEMFC, the O-PtZn/ZnNC outperforms Pt/C in both performance and durability; O-PtZn/ZnNC and Pt/C cells exhibit current densities of 71 and 39 mA cm −2 , respectively, at a cell voltage of 0.8 V. These values fall to 43 (−39 %) and 11 (−72 %) mA cm −2 , respectively, after 30 k cycles. Density functional theory calculations illustrate that ZnNC has a strong binding energy with O-PtZn (−8.13 eV) and a small interfacial minimum distance of 2.03 Å, resulting in exceptional retention of electrochemical active surface area retention for O-PtZn/ZnNC (−7%, from 57.9 to 53.8 m 2 g Pt −1 , after 30 k cycles).
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