Abstract

Pt with high coordination number (HCN) located in the defect surface sites is favorable for high oxygen reduction reaction activity. However, it is still a challenge to design and fabricate such a structure with a high density of Pt HCN sites at minimum Pt usage. Here, using nanoporous Au (NPG) that intrinsically possesses a higher proportion of HCN Au atoms over traditional nanoparticles, we epitaxially deposit Pt monolayer onto NPG to inherit the high-density HCN Pt sites. Among the NPG-Pt catalysts, the one with a smaller ligament size possesses a higher proportion of HCN Pt atoms, thus exhibiting a 5.2-fold specific activity and 18.7-fold mass activity enhancement than the commercial Pt/C catalyst. Moreover, depositing Au atoms on the NPG-Pt surface can further increase the HCN Pt surface exposure, which leads to a 6.9-fold specific activity and 19.1-fold mass activity increase as compared to Pt/C.

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