纳米孔
单层
材料科学
催化作用
外延
氧气
氧原子
纳米颗粒
铂金
纳米技术
化学工程
结晶学
图层(电子)
化学
分子
有机化学
工程类
作者
Qiwen Zhang,Jia He,Ruijie Guo,Yang Zhao,Weiqing Zhang,Wei Zhang,Su‐Seng Pang,Yi Ding
标识
DOI:10.1021/acsami.8b14079
摘要
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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