Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Fermiology and Band Structure of Oxygen-Terminated Ti3 C2 T x MXene

Magnuson, Martin ; Eklund, Per and Polley, Craig LU (2025) In Physical Review Letters 134(10).
Abstract

The class of two-dimensional carbides and nitrides known as MXenes exhibit remarkable electronic properties. Tailoring these properties, however, requires an in-depth understanding of the band structure and Fermi-surface topology. Surface oxidation of MXenes has previously hampered the characterization of their Fermi surface, which is crucial for understanding the topology and anisotropy in the electronic structure and, ultimately, for tailoring electronic properties. Here, we reveal the Fermi surface topology and band structure of purely oxygen-terminated Ti3C2Tx MXene achieved through rigorous thin film sample preparation and ultrahigh vacuum annealing. Polarized synchrotron radiation-based angle-resolved photoemission spectroscopy... (More)

The class of two-dimensional carbides and nitrides known as MXenes exhibit remarkable electronic properties. Tailoring these properties, however, requires an in-depth understanding of the band structure and Fermi-surface topology. Surface oxidation of MXenes has previously hampered the characterization of their Fermi surface, which is crucial for understanding the topology and anisotropy in the electronic structure and, ultimately, for tailoring electronic properties. Here, we reveal the Fermi surface topology and band structure of purely oxygen-terminated Ti3C2Tx MXene achieved through rigorous thin film sample preparation and ultrahigh vacuum annealing. Polarized synchrotron radiation-based angle-resolved photoemission spectroscopy reveals electron pockets, bulk band gaps, and a Dirac-like feature in the anisotropic electronic band structure. This paves the way for a fundamental understanding of band engineering of electronic transport properties, providing insights of importance for energy storage devices, transparent conductors, and catalysis.

(Less)
Please use this url to cite or link to this publication:
author
; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Physical Review Letters
volume
134
issue
10
article number
106201
publisher
American Physical Society
external identifiers
  • scopus:86000526765
  • pmid:40153641
ISSN
0031-9007
DOI
10.1103/PhysRevLett.134.106201
language
English
LU publication?
yes
id
a3932428-4eec-4708-b199-8ec64be55b6e
date added to LUP
2025-06-17 12:45:10
date last changed
2025-07-15 15:39:15
@article{a3932428-4eec-4708-b199-8ec64be55b6e,
  abstract     = {{<p>The class of two-dimensional carbides and nitrides known as MXenes exhibit remarkable electronic properties. Tailoring these properties, however, requires an in-depth understanding of the band structure and Fermi-surface topology. Surface oxidation of MXenes has previously hampered the characterization of their Fermi surface, which is crucial for understanding the topology and anisotropy in the electronic structure and, ultimately, for tailoring electronic properties. Here, we reveal the Fermi surface topology and band structure of purely oxygen-terminated Ti3C2Tx MXene achieved through rigorous thin film sample preparation and ultrahigh vacuum annealing. Polarized synchrotron radiation-based angle-resolved photoemission spectroscopy reveals electron pockets, bulk band gaps, and a Dirac-like feature in the anisotropic electronic band structure. This paves the way for a fundamental understanding of band engineering of electronic transport properties, providing insights of importance for energy storage devices, transparent conductors, and catalysis.</p>}},
  author       = {{Magnuson, Martin and Eklund, Per and Polley, Craig}},
  issn         = {{0031-9007}},
  language     = {{eng}},
  number       = {{10}},
  publisher    = {{American Physical Society}},
  series       = {{Physical Review Letters}},
  title        = {{Fermiology and Band Structure of Oxygen-Terminated Ti3 C2 T x MXene}},
  url          = {{http://dx.doi.org/10.1103/PhysRevLett.134.106201}},
  doi          = {{10.1103/PhysRevLett.134.106201}},
  volume       = {{134}},
  year         = {{2025}},
}