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High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways
Scanning transmission electron microscopy (STEM) provides structural analysis with sub-angstrom resolution. But the pixel-by-pixel scanning process is a limiting factor in acquiring high-speed data. Different strategies have been implemented to increase scanning speeds while at the same time minimiz...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8608981/ https://www.ncbi.nlm.nih.gov/pubmed/34811427 http://dx.doi.org/10.1038/s41598-021-02052-1 |
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author | Ortega, Eduardo Nicholls, Daniel Browning, Nigel D. de Jonge, Niels |
author_facet | Ortega, Eduardo Nicholls, Daniel Browning, Nigel D. de Jonge, Niels |
author_sort | Ortega, Eduardo |
collection | PubMed |
description | Scanning transmission electron microscopy (STEM) provides structural analysis with sub-angstrom resolution. But the pixel-by-pixel scanning process is a limiting factor in acquiring high-speed data. Different strategies have been implemented to increase scanning speeds while at the same time minimizing beam damage via optimizing the scanning strategy. Here, we achieve the highest possible scanning speed by eliminating the image acquisition dead time induced by the beam flyback time combined with reducing the amount of scanning pixels via sparse imaging. A calibration procedure was developed to compensate for the hysteresis of the magnetic scan coils. A combination of sparse and serpentine scanning routines was tested for a crystalline thin film, gold nanoparticles, and in an in-situ liquid phase STEM experiment. Frame rates of 92, 23 and 5.8 s(-1) were achieved for images of a width of 128, 256, and 512 pixels, respectively. The methods described here can be applied to single-particle tracking and analysis of radiation sensitive materials. |
format | Online Article Text |
id | pubmed-8608981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86089812021-11-24 High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways Ortega, Eduardo Nicholls, Daniel Browning, Nigel D. de Jonge, Niels Sci Rep Article Scanning transmission electron microscopy (STEM) provides structural analysis with sub-angstrom resolution. But the pixel-by-pixel scanning process is a limiting factor in acquiring high-speed data. Different strategies have been implemented to increase scanning speeds while at the same time minimizing beam damage via optimizing the scanning strategy. Here, we achieve the highest possible scanning speed by eliminating the image acquisition dead time induced by the beam flyback time combined with reducing the amount of scanning pixels via sparse imaging. A calibration procedure was developed to compensate for the hysteresis of the magnetic scan coils. A combination of sparse and serpentine scanning routines was tested for a crystalline thin film, gold nanoparticles, and in an in-situ liquid phase STEM experiment. Frame rates of 92, 23 and 5.8 s(-1) were achieved for images of a width of 128, 256, and 512 pixels, respectively. The methods described here can be applied to single-particle tracking and analysis of radiation sensitive materials. Nature Publishing Group UK 2021-11-22 /pmc/articles/PMC8608981/ /pubmed/34811427 http://dx.doi.org/10.1038/s41598-021-02052-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ortega, Eduardo Nicholls, Daniel Browning, Nigel D. de Jonge, Niels High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title | High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title_full | High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title_fullStr | High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title_full_unstemmed | High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title_short | High temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
title_sort | high temporal-resolution scanning transmission electron microscopy using sparse-serpentine scan pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8608981/ https://www.ncbi.nlm.nih.gov/pubmed/34811427 http://dx.doi.org/10.1038/s41598-021-02052-1 |
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