催化作用
X射线光电子能谱
材料科学
Atom(片上系统)
吸附
密度泛函理论
扫描隧道显微镜
金属
铂金
单原子气体
氧原子
纳米技术
化学工程
结晶学
化学物理
物理化学
分子
化学
计算化学
冶金
计算机科学
有机化学
工程类
嵌入式系统
作者
Filip Dvořák,Matteo Farnesi Camellone,Andrii Tovt,Nguyen-Dung Tran,Fábio R. Negreiros,Mykhailo Vorokhta,Tomáš Škála,Iva Matolı́nová,Josef Mysliveček,Vladimı́r Matolín,Stefano Fabris
摘要
Abstract Single-atom catalysts maximize the utilization of supported precious metals by exposing every single metal atom to reactants. To avoid sintering and deactivation at realistic reaction conditions, single metal atoms are stabilized by specific adsorption sites on catalyst substrates. Here we show by combining photoelectron spectroscopy, scanning tunnelling microscopy and density functional theory calculations that Pt single atoms on ceria are stabilized by the most ubiquitous defects on solid surfaces—monoatomic step edges. Pt segregation at steps leads to stable dispersions of single Pt 2+ ions in planar PtO 4 moieties incorporating excess O atoms and contributing to oxygen storage capacity of ceria. We experimentally control the step density on our samples, to maximize the coverage of monodispersed Pt 2+ and demonstrate that step engineering and step decoration represent effective strategies for understanding and design of new single-atom catalysts.
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