Perpendicular Emission, Dichroism, and Energy Dependence in Angle-Resolved Photoemission: The Importance of The Final State

被引:33
|
作者
Dauth, M. [1 ]
Graus, M. [2 ]
Schelter, I. [1 ]
Wiessner, M. [2 ]
Schoell, A. [2 ]
Reinert, F. [2 ]
Kummel, S. [1 ]
机构
[1] Univ Bayreuth, Theoret Phys 4, D-95440 Bayreuth, Germany
[2] Univ Wurzburg, Expt Phys 7, D-97074 Wurzburg, Germany
关键词
PHOTOELECTRON ANGULAR-DISTRIBUTION; DENSITY-FUNCTIONAL THEORY; CIRCULAR-DICHROISM; ELECTRONIC-STRUCTURE; MOLECULES; SPECTROSCOPY; SURFACE; TIME; PHOTOIONIZATION; SCATTERING;
D O I
10.1103/PhysRevLett.117.183001
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Angle-resolved photoemission spectroscopy has been developed to a very high accuracy. However, effects that depend sensitively on the state of the emitted photoelectron were so far hard to compute for real molecules. We here show that the real-time propagation approach to time-dependent density functional theory allows us to obtain final-state effects consistently from first principles and with an accuracy that allows for the interpretation of experimental data. In a combined theoretical and experimental study we demonstrate that the approach captures three hallmark effects that are beyond the final-state plane-wave approximation: emission perpendicular to the light polarization, circular dichroism in the photoelectron angular distribution, and a pronounced energy dependence of the photoemission intensity.
引用
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页数:6
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