悬空债券
二聚体
扫描隧道显微镜
磷化氢
吸附
材料科学
基质(水族馆)
纳米技术
Atom(片上系统)
沸石咪唑盐骨架
掺杂剂
结晶学
化学物理
兴奋剂
光电子学
化学
硅
物理化学
金属有机骨架
计算机科学
催化作用
有机化学
嵌入式系统
地质学
海洋学
生物化学
作者
Jonathan Wyrick,Xiqiao Wang,Pradeep Namboodiri,Ranjit V. Kashid,Fan Fei,Joseph M. Fox,Richard M. Silver
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-11-01
卷期号:16 (11): 19114-19123
被引量:31
标识
DOI:10.1021/acsnano.2c08162
摘要
The doping of Si using the scanning probe hydrogen depassivation lithography technique has been shown to enable placing and positioning small numbers of P atoms with nanometer accuracy. Several groups have now used this capability to build devices that exhibit desired quantum behavior determined by their atomistic details. What remains elusive, however, is the ability to control the precise number of atoms placed at a chosen site with 100% yield, thereby limiting the complexity and degree of perfection achievable. As an important step toward precise control of dopant number, we explore the adsorption of the P precursor molecule, phosphine, into atomically perfect dangling bond patches of intentionally varied size consisting of three adjacent Si dimers along a dimer row, two adjacent dimers, and one single dimer. Using low temperature scanning tunneling microscopy, we identify the adsorption products by generating and comparing to a catalog of simulated images, explore atomic manipulation after adsorption in select cases, and follow up with incorporation of P into the substrate. For one-dimer patches, we demonstrate that manipulation of the adsorbed species leads to single P incorporation in 12 out of 12 attempts. Based on the observations made in this study, we propose this one-dimer patch method as a robust approach that can be used to fabricate devices where it is ensured that each site of interest has exactly one P atom.
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