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How Circular Dichroism in time- and angle-resolved photoemission can be used to spectroscopically detect transient topological states in graphene

137   0   0.0 ( 0 )
 Added by Michael Sch\\\"uler
 Publication date 2020
  fields Physics
and research's language is English




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Pumping graphene with circularly polarized light is the archetype of light-tailoring topological bands. Realizing the induced Floquet-Chern insulator state and tracing clear experimental manifestions has been a challenge, and it has become clear that scattering effects play a crucial role. We tackle this gap between theory and experiment by employing microscopic quantum kinetic calculations including realistic electron-electron and electron-phonon scattering. Our theory provides a direct link to the build-up of the Floquet-Chern insulator state in light-driven graphene and its detection in time- and angle-resolved photoemission spectroscopy (ARPES). This allows us to study the stability of the Floquet features due to dephasing and thermalization effects. We also discuss the ultrafast Hall response in the laser-heated state. Furthermore, the induced pseudospin texture and the associated Berry curvature gives rise to momentum-dependent orbital magnetization, which is reflected in circular dichroism in ARPES (CD-ARPES). Combining our nonequilibrium calculations with an accurate one-step theory of photoemission allows us to establish a direct link between the build-up of the topological state and the dichroic pump-probe photoemission signal. The characteristic features in CD-ARPES are further corroborated to be stable against heating and dephasing effects. Thus, tracing circular dichroism in time-resolve photoemission provides new insights into transient topological properties.



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158 - Yihua Wang , Nuh Gedik 2012
Topological insulators are a new phase of matter that exhibits exotic surface electronic properties. Determining the spin texture of this class of material is of paramount importance for both fundamental understanding of its topological order and future spin-based applications. In this article, we review the recent experimental and theoretical studies on the differential coupling of left- versus right-circularly polarized light to the topological surface states in angle-resolved photoemission spectroscopy. These studies have shown that the polarization of light and the experimental geometry plays a very important role in both photocurrent intensity and spin polarization of photoelectrons emitted from the topological surface states. A general photoemission matrix element calculation with spin-orbit coupling can quantitatively explain the observations and is also applicable to topologically trivial systems. These experimental and theoretical investigations suggest that optical excitation with circularly polarized light is a promising route towards mapping the spin-orbit texture and manipulating the spin orientation in topological and other spin-orbit coupled materials.
We use angle-resolved photoemission with circularly polarized excitation to demonstrate that in the 5x1 superstructure-free Pb-Bi2212 material there are no signatures of time-reversal symmetry breaking in the sense of the criteria developed earlier (Kaminski et al. Nature {bf 416}, 610 (2002)). In addition to the existing technique, we suggest and apply an independent experimental approach to prove the absence of the effect in the studied compounds. The dichroic signal retains reflection antisymmetry as a function of temperature and doping and in all mirror planes, precisely defined by the experimental dispersion at low energies. The obtained results demonstrate that the signatures of time-reversal symmetry violation in pristine Bi2212, as determined by ARPES, are not a universal feature of all cuprate superconductors.
The helical Dirac fermions at the surface of topological insulators show a strong circular dichroism which has been explained as being due to either the initial-state spin angular momentum, the initial-state orbital angular momentum, or the handedness of the experimental setup. All of these interpretations conflict with our data from Bi2Te3 which depend on the photon energy and show several sign changes. Our one-step photoemission calculations coupled to ab initio theory confirm the sign change and assign the dichroism to a final-state effect. The spin polarization of the photoelectrons, instead, remains a reliable probe for the spin in the initial state.
162 - Y. H. Wang , D. Hsieh , D. Pilon 2011
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139 - Baiqing Lv , Tian Qian , 2021
Angle-resolved photoemission spectroscopy (ARPES), an experimental technique based on the photoelectric effect, is arguably the most powerful method for probing the electronic structure of solids. The past decade has witnessed notable progress in ARPES, including the rapid development of soft-X-ray ARPES, time-resolved ARPES, spin-resolved ARPES and spatially resolved ARPES, as well as considerable improvements in energy and momentum resolution. Consequently , ARPES has emerged as an indispensable experimental probe in the study of topological materials, which have characteristic non-trivial bulk and surface electronic structures that can be directly detected by ARPES. Over the past few years, ARPES has had a crucial role in several landmark discoveries in topological materials, including the identification of topological insulators and topological Dirac and Weyl semimetals. In this Technical Review , we assess the latest developments in different ARPES techniques and illustrate the capabilities of these techniques with applications in the study of topological materials.
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