It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Advances in electron microscopy have enabled visualizations of the three-dimensional (3D) atom arrangements in nano-scale objects. The observations are, however, prone to electron-beam-induced object alterations, so tracking of single atoms in space and time becomes key to unravel inherent structures and properties. Here, we introduce an analytical approach to quantitatively account for atom dynamics in 3D atomic-resolution imaging. The approach is showcased for a Co-Mo-S nanocrystal by analysis of time-resolved in-line holograms achieving ~1.5 Å resolution in 3D. The analysis reveals a decay of phase image contrast towards the nanocrystal edges and meta-stable edge motifs with crystallographic dependence. These findings are explained by beam-stimulated vibrations that exceed Debye-Waller factors and cause chemical transformations at catalytically relevant edges. This ability to simultaneously probe atom vibrations and displacements enables a recovery of the pristine Co-Mo-S structure and establishes, in turn, a foundation to understand heterogeneous chemical functionality of nanostructures, surfaces and molecules.
The authors introduce an analytical approach for quantitative analysis of 3D atom dynamics during electron microscopy. They image a Co-Mo-S nanocrystal with 1.5 Å resolution, and observe chemical transformations caused by beam-stimulated vibrations.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details




1 City University of Hong Kong, Department of Materials Science and Engineering, Kowloon Tong, Hong Kong, SAR (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846)
2 EMAT, University of Antwerp, Antwerp, Belgium (GRID:grid.5284.b) (ISNI:0000 0001 0790 3681)
3 Lawrence Berkeley National Laboratory, The Molecular Foundry, Berkeley, USA (GRID:grid.184769.5) (ISNI:0000 0001 2231 4551)
4 Haldor Topsoe A/S, Haldor Topsøes Allé 1, Kgs. Lyngby, Denmark (GRID:grid.424590.e) (ISNI:0000 0004 0607 9629)
5 Haldor Topsoe A/S, Haldor Topsøes Allé 1, Kgs. Lyngby, Denmark (GRID:grid.424590.e) (ISNI:0000 0004 0607 9629); Technical University of Denmark, Center for Visualizing Catalytic Processes (VISION), Department of Physics, Kgs. Lyngby, Denmark (GRID:grid.5170.3) (ISNI:0000 0001 2181 8870)