Using electron energy-loss spectroscopy to measure nanoscale electronic and vibrational dynamics in a TEM

被引:5
|
作者
Kim, Ye-Jin [1 ]
Palmer, Levi D. D. [1 ]
Lee, Wonseok [1 ]
Heller, Nicholas J. J. [1 ]
Cushing, Scott K. K. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 159卷 / 05期
基金
美国国家科学基金会;
关键词
OXIDATION-STATE; ULTRAFAST; DENSITY; EXCITATIONS; RESOLUTION; DETECTORS; PLASMONS; CARRIERS; STEM;
D O I
10.1063/5.0147356
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electron energy-loss spectroscopy (EELS) can measure similar information to x-ray, UV-Vis, and IR spectroscopies but with atomic resolution and increased scattering cross-sections. Recent advances in electron monochromators have expanded EELS capabilities from chemical identification to the realms of synchrotron-level core-loss measurements and to low-loss, 10-100 meV excitations, such as phonons, excitons, and valence structures. EELS measurements are easily correlated with electron diffraction and atomic-scale real-space imaging in a transmission electron microscope (TEM) to provide detailed local pictures of quasiparticle and bonding states. This perspective provides an overview of existing high-resolution EELS (HR-EELS) capabilities while also motivating the powerful next step in the field-ultrafast EELS in a TEM. Ultrafast EELS aims to combine atomic-level, element-specific, and correlated temporal measurements to better understand spatially specific excited-state phenomena. Ultrafast EELS measurements also add to the abilities of steady-state HR-EELS by being able to image the electromagnetic field and use electrons to excite photon-forbidden and momentum-specific transitions. We discuss the technical challenges ultrafast HR-EELS currently faces, as well as how integration with in situ and cryo measurements could expand the technique to new systems of interest, especially molecular and biological samples.
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页数:13
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