聚结(物理)
一氧化碳
成核
催化作用
化学物理
星团(航天器)
表面扩散
材料科学
金属
烧结
离解(化学)
扫描隧道显微镜
分子
Atom(片上系统)
化学工程
吸附
化学
纳米技术
物理化学
冶金
嵌入式系统
计算机科学
有机化学
工程类
程序设计语言
物理
天体生物学
作者
Gareth S. Parkinson,Zbyněk Novotný,Giacomo Argentero,Michael Schmid,Jiří Pavelec,Rukan Kosak,Peter Blaha,Ulrike Diebold
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2013-06-07
卷期号:12 (8): 724-728
被引量:289
摘要
The coarsening of catalytically active metal clusters is often accelerated by the presence of gases, but the role played by gas molecules is difficult to ascertain and varies from system to system. We use scanning tunnelling microscopy to follow the CO-induced coalescence of Pd adatoms supported on the Fe3O4(001) surface at room temperature, and find Pd-carbonyl species to be responsible for mobility in this system. Once these reach a critical density, clusters nucleate; subsequent coarsening occurs through cluster diffusion and coalescence. Whereas CO induces the mobility in the Pd/Fe3O4 system, surface hydroxyls have the opposite effect. Pd atoms transported to surface OH groups are no longer susceptible to carbonyl formation and remain isolated. Following the evolution from well-dispersed metal adatoms into clusters, atom-by-atom, allows identification of the key processes that underlie gas-induced mass transport.
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