黑磷
悬空债券
原子单位
扫描隧道显微镜
降级(电信)
化学物理
电子结构
材料科学
氧气
纳米技术
化学
密度泛函理论
光谱学
化学工程
分析化学(期刊)
光电子学
计算化学
环境化学
硅
有机化学
工程类
物理
电信
量子力学
计算机科学
作者
Ben St Laurent,Dibyendu Dey,Liping Yu,Shawna M. Hollen
标识
DOI:10.1021/acsaelm.1c00558
摘要
Black phosphorus (BP) exhibits extraordinary electronic properties that are desirable for a wide variety of electronic and optoelectronic applications. However, applications of BP are hindered by its rapid degradation in ambient conditions. Despite significant advances that have been made in understanding the degradation mechanism, no consensus has yet been reached on how BP oxidation occurs at the atomic scale as experimental studies have been mostly restricted to averaged effects of degradation over a micron- to millimeter-sized region. Here, BP oxidation is investigated using scanning tunneling microscopy/spectroscopy (STM/S). Introducing O2 gas to the BP surface in ultrahigh vacuum at a pressure of 10–5 mbar for 1 min creates two new types of defects on the surface. We identify these defects as dangling atomic oxygen and phosphorus multivacancies using density functional theory simulations. In addition to the structural changes to the surface, the electronic structure is also drastically altered by the introduction of oxygen. The 300 meV band gap of BP is lifted due to dosing. This change in the electronic structure is reversible through STM tip manipulation. These are the first experimental results showing the atomic-scale oxidation of BP, an important step toward understanding the degradation process.
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