Indications of chemical bond contrast in AFM images of a hydrogen-terminated silicon surface

被引:26
|
作者
Labidi, Hatem [1 ,2 ]
Koleini, Mohammad [1 ,2 ]
Huff, Taleana [1 ]
Salomons, Mark [2 ]
Cloutier, Martin [2 ]
Pitters, Jason [2 ]
Wolkow, Robert A. [1 ,2 ]
机构
[1] Univ Alberta, Dept Phys, Edmonton, AB T6G 2J1, Canada
[2] Natl Res Council Canada, Natl Inst Nanotechnol, Edmonton, AB T6G 2M9, Canada
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
加拿大自然科学与工程研究理事会;
关键词
ATOMIC-FORCE MICROSCOPY; SCANNING-TUNNELING-MICROSCOPY; MOLECULAR-DYNAMICS; RESOLUTION; SI(100);
D O I
10.1038/ncomms14222
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The origin of bond-resolved atomic force microscope images remains controversial. Moreover, most work to date has involved planar, conjugated hydrocarbon molecules on a metal substrate thereby limiting knowledge of the generality of findings made about the imaging mechanism. Here we report the study of a very different sample; a hydrogen-terminated silicon surface. A procedure to obtain a passivated hydrogen-functionalized tip is defined and evolution of atomic force microscopy images at different tip elevations are shown. At relatively large tip-sample distances, the topmost atoms appear as distinct protrusions. However, on decreasing the tip-sample distance, features consistent with the silicon covalent bonds of the surface emerge. Using a density functional tight-binding-based method to simulate atomic force microscopy images, we reproduce the experimental results. The role of the tip flexibility and the nature of bonds and false bond-like features are discussed.
引用
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页数:7
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