CO tip functionalization in subatomic resolution atomic force microscopy

被引:5
|
作者
Kim, Minjung [1 ]
Chelikowsky, James R. [2 ,3 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Computat Engn & Sci, Ctr Computat Mat, Austin, TX 78712 USA
[3] Univ Texas Austin, Dept Phys & Chem Engn, Austin, TX 78712 USA
关键词
ELECTRONIC-STRUCTURE CALCULATIONS; CHEMICAL-STRUCTURE; IDENTIFICATION;
D O I
10.1063/1.4934273
中图分类号
O59 [应用物理学];
学科分类号
摘要
Noncontact atomic force microscopy (nc-AFM) employing a CO-functionalized tip displays dramatically enhanced resolution wherein covalent bonds of polycyclic aromatic hydrocarbon can be imaged. Employing real-space pseudopotential first-principles calculations, we examine the role of CO in functionalizing the nc-AFM tip. Our calculations allow us to simulate full AFM images and ascertain the enhancement mechanism of the CO molecule. We consider two approaches: one with an explicit inclusion of the CO molecule and one without. By comparing our simulations to existing experimental images, we ascribe the enhanced resolution of the CO functionalized tip to the special orbital characteristics of the CO molecule. (C) 2015 AIP Publishing LLC.
引用
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页数:4
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