Core–shell catalysts consisting of nanoporous cores for oxygen reduction reaction

催化作用 溶解 纳米孔 材料科学 纳米颗粒 电化学 化学工程 透射电子显微镜 多孔性 扫描透射电子显微镜 粒子(生态学) 粒径 纳米技术 化学 电极 复合材料 物理化学 有机化学 海洋学 地质学 工程类
作者
Minhua Shao,Brandon H. Smith,Sandra Guerrero,Lesia Protsailo,Dong Su,Keiichi Kaneko,Jonathan H. Odell,Michael P. Humbert,Kotaro Sasaki,Jesse Michael Marzullo,Robert M. Darling
出处
期刊:Physical Chemistry Chemical Physics [The Royal Society of Chemistry]
卷期号:15 (36): 15078-15078 被引量:30
标识
DOI:10.1039/c3cp52252k
摘要

A comprehensive experimental study was conducted on the dealloying of PdNi6 nanoparticles under various conditions. A two-stage dealloying protocol was developed to leach >95% of Ni while minimizing the dissolution of Pd. The final structure of the dealloyed particle was strongly dependent on the acid used and temperature. When H2SO4 and HNO3 solutions were used in the first stage of dealloying, solid and porous particles were generated, respectively. The porous particles have a 3-fold higher electrochemical surface area per Pd mass than the solid ones. The dealloyed PdNi6 nanoparticles were then used as a core material for the synthesis of core–shell catalysts. These catalysts were synthesized in gram-size batches and involved Pt displacement of an underpotentially deposited (UPD) Cu monolayer. The resulting materials were characterized by scanning transmission electron microscopy (STEM) and in situ X-ray diffraction (XRD). The oxygen reduction reaction (ORR) activity of the core–shell catalysts is 7-fold higher than the state-of-the-art Pt/C. The high activity was confirmed by a more than 40 mV improvement in fuel cell performance with a Pt loading of 0.1 mg cm−2 by using the core–shell catalysts.
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