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

被引:151
作者
Carbone, Fabrizio [1 ]
Kwon, Oh-Hoon [1 ]
Zewail, Ahmed H. [1 ]
机构
[1] CALTECH, Arthur Amos Noyes Lab Chem Phys, Phys Biol Ctr Ultrafast Sci & Technol, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
LOSS SPECTROSCOPY; TIME; REAL; XANES; SPACE; EELS;
D O I
10.1126/science.1175005
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 sp(2) [two-dimensional (2D) graphene] to sp(3) (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.
引用
收藏
页码:181 / 184
页数:4
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