scholarly journals Local atomic structure determination using focused electron beams

2014 ◽  
Vol 70 (a1) ◽  
pp. C26-C26
Author(s):  
Joanne Etheridge
Keyword(s):  
Quantum Wells ◽  
Atomic Structure ◽  
Structural Information ◽  
Electron Beams ◽  
Focal Point ◽  
Local Atomic Structure ◽  
Atomic Scale ◽  
Chemical Information ◽  
Diffraction Patterns

This talk will give an overview of methods for solving the atomic structure of nanostructured materials using focused electron beams. It will illustrate these methods with a range of applications, such as the determination of the atomic structure and stability of nanoparticle facets [1]; the local atomic structure of "chessboard' nanostructures in lithium-based titanate perovskites; and the measurement of local polarity, dopant concentration and atomic-scale morphology in semiconducting nanowire quantum wells. These methods take advantage of the fact that electron wavefields can be brought to a focal point smaller than an Ångström in diameter, enabling small volumes of matter to be probed and characterized. The wealth of information contained in the resulting diffraction patterns can be interrogated selectively to isolate and `image' specific structural information. Several methods using small focused electron beams will be described in this talk, including; (i) An approach for the determination of centrosymmetric structures from the direct observation of structure factor phases by inspection of features in convergent beam electron diffraction patterns [2]. The method can achieve high resolution from just a few phase observations and no intensity measurements or iterative refinements are required; (ii) Methods for the quantitative interpretation of the intensity in atomic resolution imaging and diffraction data for the measurement of local atomic and electronic structure; (iii) Pseudo-confocal scanning transmission electron microscopy methods for obtaining depth and chemical information which record the scattered intensity in a plane conjugate to the specimen (as opposed to the diffraction plane) [3].

scholarly journals Reconstruction from limited single-particle diffraction data via simultaneous determination of state, orientation, intensity, and phase

2017 ◽  
Vol 114 (28) ◽  
pp. 7222-7227 ◽  
Author(s):  
Jeffrey J. Donatelli ◽  
James A. Sethian ◽  
Peter H. Zwart
Keyword(s):  
Diffraction Data ◽  
Single Particle ◽  
Structural Information ◽  
Real Space ◽  
Underlying Structure ◽  
X Ray Diffraction ◽  
Single Particles ◽  
State Orientation ◽  
Diffraction Patterns

Free-electron lasers now have the ability to collect X-ray diffraction patterns from individual molecules; however, each sample is delivered at unknown orientation and may be in one of several conformational states, each with a different molecular structure. Hit rates are often low, typically around 0.1%, limiting the number of useful images that can be collected. Determining accurate structural information requires classifying and orienting each image, accurately assembling them into a 3D diffraction intensity function, and determining missing phase information. Additionally, single particles typically scatter very few photons, leading to high image noise levels. We develop a multitiered iterative phasing algorithm to reconstruct structural information from single-particle diffraction data by simultaneously determining the states, orientations, intensities, phases, and underlying structure in a single iterative procedure. We leverage real-space constraints on the structure to help guide optimization and reconstruct underlying structure from very few images with excellent global convergence properties. We show that this approach can determine structural resolution beyond what is suggested by standard Shannon sampling arguments for ideal images and is also robust to noise.

EXAFS determination of local atomic structure of selected transition metals in CdSe matrix

1999 ◽  
Vol 286 (1-2) ◽  
pp. 89-92 ◽  
Author(s):  
K. Lawniczak–Jablonska ◽  
J. Libera ◽  
R.J. Iwanowski
Keyword(s):  
Transition Metals ◽  
Atomic Structure ◽  
Local Atomic Structure

scholarly journals Atomic Scale Structure and Chemistry of Interfaces by Z-Contrast Imaging and Electron Energy Loss Spectroscopy in the Stem

1994 ◽  
Vol 341 ◽  
Author(s):  
M. M. McGibbon ◽  
N. D. Browning ◽  
M. F. Chisholm ◽  
A. J. McGibbon ◽  
S. J. Pennycook ◽  
...  
Keyword(s):  
High Resolution ◽  
Energy Loss ◽  
Electron Energy ◽  
Atomic Structure ◽  
Electron Energy Loss Spectroscopy ◽  
Atomic Scale ◽  
Chemical Information ◽  
Contrast Imaging ◽  
Z Contrast ◽  
Electron Energy Loss

AbstractThe macroscopic properties of many materials are controlled by the structure and chemistry at grain boundaries. A basic understanding of the structure-property relationship requires a technique which probes both composition and chemical bonding on an atomic scale. High-resolution Z-contrast imaging in the scanning transmission electron microscope (STEM) forms an incoherent image in which changes in atomic structure and composition across an interface can be interpreted directly without the need for preconceived atomic structure models (1). Since the Z-contrast image is formed by electrons scattered through high angles, parallel detection electron energy loss spectroscopy (PEELS) can be used simultaneously to provide complementary chemical information on an atomic scale (2). The fine structure in the PEEL spectra can be used to investigate the local electronic structure and the nature of the bonding across the interface (3). In this paper we use the complimentary techniques of high resolution Zcontrast imaging and PEELS to investigate the atomic structure and chemistry of a 25° symmetric tilt boundary in a bicrystal of the electroceramic SrTiO3.

Coherent diffraction imaging: consistency of the assembled three-dimensional distribution

2016 ◽  
Vol 72 (4) ◽  
pp. 459-464 ◽  
Author(s):  
Miklós Tegze ◽  
Gábor Bortel
Keyword(s):  
Structural Information ◽  
Three Dimensional ◽  
Atomic Scale ◽  
Short Pulses ◽  
X Ray ◽  
Coherent Diffraction Imaging ◽  
Imaging Experiment ◽  
Dimensional Distribution ◽  
Diffraction Imaging ◽  
Diffraction Patterns

The short pulses of X-ray free-electron lasers can produce diffraction patterns with structural information before radiation damage destroys the particle. From the recorded diffraction patterns the structure of particles or molecules can be determined on the nano- or even atomic scale. In a coherent diffraction imaging experiment thousands of diffraction patterns of identical particles are recorded and assembled into a three-dimensional distribution which is subsequently used to solve the structure of the particle. It is essential to know, but not always obvious, that the assembled three-dimensional reciprocal-space intensity distribution is really consistent with the measured diffraction patterns. This paper shows that, with the use of correlation maps and a single parameter calculated from them, the consistency of the three-dimensional distribution can be reliably validated.

Development of a 200kV Atomic Resolution Analytical Electron Microscope

2009 ◽  
Vol 17 (3) ◽  
pp. 8-11 ◽  
Author(s):  
T. Isabell ◽  
J. Brink ◽  
M. Kawasaki ◽  
B. Armbruster ◽  
I. Ishikawa ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Atomic Structure ◽  
Spherical Aberration ◽  
Atomic Level ◽  
Atomic Scale ◽  
Atomic Resolution ◽  
Analytical Electron ◽  
Analytical Electron Microscope

Few electron optical inventions have revolutionized the TEM/ STEM as profoundly as the spherical aberration (Cs) corrector has. Characterization of technologically important materials increasingly needs to be done at the atomic or even sub-atomic level. This characterization includes determination of atomic structure as well as structural chemistry. With Cs correctors, the sub-Angstrom imaging barrier has been passed, and fast atomic scale spectroscopy is possible. In addition to improvements in resolution, Cs correctors offer a number of other significant improvements and benefits.

Atomic-resolution characterization of an SrTiO3 grain boundary in the STEM

1994 ◽  
Vol 52 ◽  
pp. 972-973
Author(s):  
M. M. McGibbon ◽  
N. D. Browning ◽  
M. F. Chisholm ◽  
A. J. McGibbon ◽  
S. J. Pennycook ◽  
...  
Keyword(s):  
High Resolution ◽  
Atomic Structure ◽  
Scanning Transmission Electron Microscope ◽  
Tilt Boundary ◽  
Atomic Scale ◽  
Chemical Information ◽  
Contrast Imaging ◽  
Scanning Transmission ◽  
Z Contrast ◽  
Contrast Image

High-resolution Z-contrast imaging in the scanning transmission electron microscope (STEM) forms an incoherent image in which changes in atomic structure and composition across an interface can be interpreted intuitively without the need for preconcieved atomic structure models. Since the Z-contrast image is formed by electrons scattered through high angles, parallel detection electron energy loss spectroscopy (PEELS) can be used simultaneously to provide complementary chemical information on an atomic scale. The fine structure in the PEEL spectra can be used to investigate the local electronic structure and the nature of the bonding across the interface. In this paper we use the complimentary techniques of high resolution Z-contrast imaging and PEELS to investigate the atomic structure and chemistry of a 25 degree symmetric tilt boundary in a bicrystal of the electroceramic SrTiO3.Figure 1(a) shows a Z-contrast image of a symmetric region of the tilt boundary. The brightest spots in the image correspond to the increased scattering power of the Sr atomic columns (Z=38) with theless bright spots corresponding to the Ti atomic columns (Z=22). The lighter O atomic columns are notvisible in a Z-contrast image.

Sign in / Sign up

Export Citation Format

Share Document