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High-order replica bands in monolayer FeSe/SrTiO3 revealed by polarization-dependent photoemission spectroscopy.

Authors :
Liu, Chong
Day, Ryan P.
Li, Fengmiao
Roemer, Ryan L.
Zhdanovich, Sergey
Gorovikov, Sergey
Pedersen, Tor M.
Jiang, Juan
Lee, Sangjae
Schneider, Michael
Wong, Doug
Dosanjh, Pinder
Walker, Frederick J.
Ahn, Charles H.
Levy, Giorgio
Damascelli, Andrea
Sawatzky, George A.
Zou, Ke
Source :
Nature Communications; 7/28/2021, Vol. 12 Issue 1, p1-8, 8p
Publication Year :
2021

Abstract

The mechanism of the enhanced superconductivity in monolayer FeSe/SrTiO<subscript>3</subscript> has been enthusiastically studied and debated over the past decade. One specific observation has been taken to be of central importance: the replica bands in the photoemission spectrum. Although suggestive of electron-phonon interaction in the material, the essence of these spectroscopic features remains highly controversial. In this work, we conduct angle-resolved photoemission spectroscopy measurements on monolayer FeSe/SrTiO<subscript>3</subscript> using linearly polarized photons. This configuration enables unambiguous characterization of the valence electronic structure with a suppression of the spectral background. We consistently observe high-order replica bands derived from various Fe 3d bands, similar to those observed on bare SrTiO<subscript>3</subscript>. The intensity of the replica bands is unexpectedly high and different between d<subscript>xy</subscript> and d<subscript>yz</subscript> bands. Our results provide new insights on the electronic structure of this high-temperature superconductor and the physical origin of the photoemission replica bands. The origin of the photoemission replica bands in monolayer FeSe/SrTiO<subscript>3</subscript> remains controversial. Here, the authors perform angle-resolved photoemission spectroscopy with polarized photon on FeSe/SrTiO<subscript>3</subscript> and observe high-order replica bands with high intensity from various Fe 3d bands, suggesting a mixed mechanism. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
12
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
151648305
Full Text :
https://doi.org/10.1038/s41467-021-24783-5