Related Experiment Video
Updated: Feb 1, 2026

08:30
Preparation of Graphene-Supported Microwell Liquid Cells for In Situ Transmission Electron Microscopy
Published on: July 15, 2019
10.6K
Moiré structures in twisted bilayer graphene studied by transmission electron microscopy
Tatiana Latychevskaia1, Conrad Escher1, Hans-Werner Fink1
1Institute of Physics, University of Zurich, Winterthurerstrasse 190, Zurich, 8057, Switzerland.
Ultramicroscopy
|November 30, 2018
Summary
Imaging twisted bilayer graphene (TBG) moiré structures requires low-energy electrons for observable diffraction peaks. This technique enhances graphene
Area of Science:
- Materials Science
- Condensed Matter Physics
- Nanotechnology
Background:
- Twisted bilayer graphene (TBG) exhibits moiré structures crucial for its electronic properties.
- Conventional transmission electron microscopy (TEM) at high energies (80-300 keV) does not reveal moiré periodicity in diffraction patterns.
- Understanding moiré structure imaging is key for advanced graphene applications.
Purpose of the Study:
- To investigate moiré structure imaging in free-standing TBG using TEM.
- To determine the optimal electron energy for observing moiré diffraction patterns.
- To explore the utility of Gabor holography for analyzing atomic arrangements in TBG.
Main Methods:
- Transmission electron microscopy (TEM) in diffraction mode.
- In-line Gabor holography.
- Utilizing low-energy electron diffraction (LEED) in the range of tens of eV.
- Acquiring diffraction patterns at 236 eV.
Main Results:
- High-energy electron diffraction (80-300 keV) shows peaks from individual graphene layers but not moiré patterns.
- Low-energy electrons (e.g., 236 eV) reveal distinct diffraction peaks corresponding to the moiré structure periodicity.
- Gabor holography demonstrates intensity variations in the far-field related to atomic stacking (AA/AB), not necessarily absorption.
Conclusions:
- Low-energy electron diffraction is essential for imaging moiré structures in TBG.
- Intensity changes in Gabor holography are linked to atomic arrangement, offering insights beyond absorption.
- These findings are significant for utilizing graphene as a support in electron imaging techniques.
Related Concept Videos
Transmission Electron Microscopy
7.2K
In 1931, physicist Ernst Ruska—building on the idea that magnetic fields can direct an electron beam just as lenses can direct a beam of light in an optical microscope—developed the first prototype of the electron microscope. This development led to the development of the field of electron microscopy. In the transmission electron microscope (TEM), electrons are produced by a hot tungsten element and accelerated by a potential difference in an electron gun, which gives them up to 400...
7.2K
Electronic Structure of Atoms
28.7K
An atom comprises protons and neutrons, which are contained inside the dense, central core called the nucleus, with electrons present around the nucleus. Taking into account the wave–particle duality of electrons and the uncertainty in position around the nucleus, quantum mechanics provides a more accurate model for the atomic structure. It describes atomic orbitals as the regions around the nucleus where electrons of discrete energy exist, characterized by four quantum...
28.7K
Overview of Electron Microscopy
14.6K
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
14.6K
Scanning Electron Microscopy
5.5K
A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
Fundamental Principles
Accelerated...
5.5K
Immunogold Electron Microscopy
5.5K
Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
5.5K
Cryo-electron Microscopy
4.3K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
4.3K

