Citation: Kim, S.; Moon, D.; Jeon,
B.R.; Yeon, J.; Li, X.; Kim, S. Accurate
Atomic-Scale Imaging of
Two-Dimensional Lattices Using
Atomic Force Microscopy in Ambient
Conditions. Nanomaterials 2022, 12,
1542. https://doi.org/10.3390/
nano12091542
Academic Editor: Christophe Petit
Received: 11 April 2022
Accepted: 29 April 2022
Published: 2 May 2022
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nanomaterials
Article
Accurate Atomic-Scale Imaging of Two-Dimensional Lattices
Using Atomic Force Microscopy in Ambient Conditions
Sunghyun Kim
1,†
, Donghyeon Moon
2,†
, Bo Ram Jeon
1
, Jegyeong Yeon
1
, Xiaoqin Li
3,4
and Suenne Kim
2,
*
1
Department of Applied Physics, Hanyang University, Ansan 15588, Korea; shdak6990@gmail.com (S.K.);
brhu1018@gmail.com (B.R.J.); jaekyeong.yeon@gmail.com (J.Y.)
2
Department of Photonics and Nanoelectronics, Hanyang University, Ansan 15588, Korea;
dhm227@hanyang.ac.kr
3
Center for Complex Quantum Systems, Department of Physics, The University of Texas at Austin,
Austin, TX 78712, USA; elaineli@physics.utexas.edu
4
Texas Materials Institute, The University of Texas at Austin, Austin, TX 78712, USA
* Correspondence: skim446@hanyang.ac.kr; Tel.: +82-31-400-5472
† These authors contributed equally to this work.
Abstract: To facilitate the rapid development of van der Waals materials and heterostructures, scan-
ning probe methods capable of nondestructively visualizing atomic lattices and moiré superlattices
are highly desirable. Lateral force microscopy (LFM), which measures nanoscale friction based on
the commonly available atomic force microscopy (AFM), can be used for imaging a wide range of
two-dimensional (2D) materials, but imaging atomic lattices using this technique is difficult. Here,
we examined a number of the common challenges encountered in LFM experiments and presented
a universal protocol for obtaining reliable atomic-scale images of 2D materials under ambient en-
vironment. By studying a series of LFM images of graphene and transition metal dichalcogenides
(TMDs), we have found that the accuracy and the contrast of atomic-scale images critically depended
on several scanning parameters including the scan size and the scan rate. We applied this protocol to
investigate the atomic structure of the ripped and self-folded edges of graphene and have found that
these edges were mostly in the armchair direction. This finding is consistent with the results of several
simulations results. Our study will guide the extensive effort on assembly and characterization of
new 2D materials and heterostructures.
Keywords: AFM; TMD; LFM; graphene; transition metal dichalcogenides; atomic-scale imaging
1. Introduction
In recent years, atomically thin layers and heterostructures of van der Waals (vdW) ma-
terials prepared via chemical vapor deposition (CVD) or mechanical exfoliation/stacking
have been intensively studied because of their unique properties and potential applications
in quantum electronics and nanophotonics [1–4]. By changing the number of layers or
controlling the twist angle between adjacent layers [5–7], remarkable quantum phases
and properties have been discovered, including unconventional superconductivity [8,9],
Hofstadter’s butterfly effect [10–12], Mott transition in graphene bilayers [7,13], and quan-
tized exciton states in moiré crystals formed by twisting transition metal dichalcogenides
(TMD) bilayers [14–17]. However, wrinkles and bubbles inevitably exist in stacked vdW
bilayers [18–20], causing undesirable spatial variations in strains and disorder in moiré su-
perlattices. Ultrafast laser nondestructive technology allows the study of strain, stress, and
structural properties currently on the scale of tens to hundreds of nanometers [21–24]. The
possibility of imaging atomic-scale strain-induced lattice distortion [25] or even controlling
the twist angle using scanning probe methods [10] has been demonstrated. Nevertheless,
such experiments remain very challenging in general.
Nanomaterials 2022, 12, 1542. https://doi.org/10.3390/nano12091542 https://www.mdpi.com/journal/nanomaterials