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Dynamics of Chemical Bonding Mapped by Energy-Resolved 4D Electron Microscopy

2009/07/09 by Fabrizio Carbone, Oh‐Hoon Kwon, Ahmed H. Zewail · 1 citation
Biochemistry, Genetics and Molecular Biology · Materials Science · Physics and Astronomy · #Advanced Electron Microscopy Techniques and Applications #Diamond and Carbon-based Materials Research #Quantum and electron transport phenomena

paper · doi:10.1126/science.1175005

openalex publication_date 2009/07/09 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/23

Abstract

Chemical bonding dynamics are fundamental to the understanding of properties and behavior of materials and molecules. Here, we demonstrate the potential of time-resolved, femtosecond electron energy loss spectroscopy (EELS) for mapping electronic structural changes in the course of nuclear motions. For graphite, it is found that changes of milli-electron volts in the energy range of up to 50 electron volts reveal the compression and expansion of layers on the subpicometer scale (for surface and bulk atoms). These nonequilibrium structural features are correlated with the direction of change from sp2 [two-dimensional (2D) graphene] to sp3 (3D-diamond) electronic hybridization, and the results are compared with theoretical charge-density calculations. The reported femtosecond time resolution of four-dimensional (4D) electron microscopy represents an advance of 10 orders of magnitude over that of conventional EELS methods.

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