磷烯
扫描隧道显微镜
磷化物
材料科学
图层(电子)
化学物理
结晶学
相(物质)
沉积(地质)
铜
纳米技术
金属
化学
冶金
地质学
有机化学
古生物学
沉积物
单层
作者
Jiří David,František Jeřábek,Pavel Procházka,Miroslav Černý,Cristian V. Ciobanu,Stanislav Průša,Tomáš Šikola,Suneel Kodambaka,Miroslav Kolı́bal
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-22
标识
DOI:10.1021/acsnano.4c11802
摘要
Blue phosphorene, a two-dimensional, hexagonal-structured, semiconducting phosphorus, has gained attention as it is considered easier to synthesize on metal surfaces than its allotrope, black phosphorene. Recent studies report different structures of phosphorene, for example, on Cu(111), but the underlying mechanisms of their formation are not known. Here, using a combination of in situ ultrahigh vacuum low-energy electron microscopy and in vacuo scanning tunneling microscopy, we determine the time evolution of the surface structure and morphology during the deposition of phosphorus on single-crystalline Cu(111). We find that during the early stages of deposition phosphorus intermixes with Cu, resulting in copper phosphide structures. With the increasing surface concentration of phosphorus, the phosphide phase disappears, and a blue phosphorene layer forms, followed by the self-assembly of highly ordered phosphorus clusters that eventually grow into multilayer islands. We attribute the unexpected transformation of stable phosphide to a phosphorene layer to the presence of a large concentration of P2 dimers on the surface. Our results constitute direct evidence for a growth mode leading to a flat phosphorene layer via an intermediary phase, which could underpin the growth of other 2D materials on strongly interacting substrates.
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