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.
引用
收藏
页数:13
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