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Emergence of two distinct phase transitions in monolayer CoSe2 on graphene

Authors :
Tae Gyu Rhee
Nguyen Huu Lam
Yeong Gwang Kim
Minseon Gu
Jinwoong Hwang
Aaron Bostwick
Sung-Kwan Mo
Seung-Hyun Chun
Jungdae Kim
Young Jun Chang
Byoung Ki Choi
Source :
Nano Convergence, Vol 11, Iss 1, Pp 1-8 (2024)
Publication Year :
2024
Publisher :
SpringerOpen, 2024.

Abstract

Abstract Dimensional modifications play a crucial role in various applications, especially in the context of device miniaturization, giving rise to novel quantum phenomena. The many-body dynamics induced by dimensional modifications, including electron-electron, electron-phonon, electron-magnon and electron-plasmon coupling, are known to significantly affect the atomic and electronic properties of the materials. By reducing the dimensionality of orthorhombic CoSe2 and forming heterostructure with bilayer graphene using molecular beam epitaxy, we unveil the emergence of two types of phase transitions through angle-resolved photoemission spectroscopy and scanning tunneling microscopy measurements. We disclose that the 2 × 1 superstructure is associated with charge density wave induced by Fermi surface nesting, characterized by a transition temperature of 340 K. Additionally, another phase transition at temperature of 160 K based on temperature dependent gap evolution are observed with renormalized electronic structure induced by electron-boson coupling. These discoveries of the electronic and atomic modifications, influenced by electron-electron and electron-boson interactions, underscore that many-body physics play significant roles in understanding low-dimensional properties of non-van der Waals Co-chalcogenides and related heterostructures. Graphical Abstract

Details

Language :
English
ISSN :
21965404
Volume :
11
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nano Convergence
Publication Type :
Academic Journal
Accession number :
edsdoj.1a97dc4b8bc490da8849bd456ed2b5e
Document Type :
article
Full Text :
https://doi.org/10.1186/s40580-024-00427-4