Nanoscale determination of the metal-insulator transition in intercalated bulk VSe$_{2}$

Fuente: arXiv
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Auteurs principaux: Ma, Wanru, Yang, Ye, Liang, Zuowei, Wu, Ping, Meng, Fanbao, Wang, Zhenyu, Chen, Xianhui
Format: Preprint
Publié: 2025
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author Ma, Wanru
Yang, Ye
Liang, Zuowei
Wu, Ping
Meng, Fanbao
Wang, Zhenyu
Chen, Xianhui
author_facet Ma, Wanru
Yang, Ye
Liang, Zuowei
Wu, Ping
Meng, Fanbao
Wang, Zhenyu
Chen, Xianhui
contents Two-dimensional (2D) materials provide unique opportunities to realize emergent phenomena by reducing dimensionality. Using scanning tunneling microscopy combined with first-principles calculations, we determine an intriguing case of a metal-insulator transition (MIT) in a bulk compound, (TBA)$_{0.3}$VSe$_2$. Atomic-scale imaging reveals that the initial $4a_0 \times 4a_0$ charge density wave (CDW) order in 1T-VSe$_2$ transforms to $\sqrt{7}a_0 \times \sqrt{3}a_0$ ordering upon intercalation, which is associated with an insulating gap with a magnitude of up to approximately 115 meV. Our calculations reveal that this energy gap is highly tunable through electron doping introduced by the intercalant. Moreover, the robustness of the $\sqrt{7}a_0 \times \sqrt{3}a_0$ CDW order against the Lifshitz transition points to the key role of electron-phonon interactions in stabilizing the CDW state. Our work clarifies a rare example of a CDW-driven MIT in quasi-2D materials and establishes cation intercalation as an effective pathway for tuning both the dimensionality and the carrier concentration without inducing strain or disorder.
format Preprint
id arxiv_https___arxiv_org_abs_2512_23264
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Nanoscale determination of the metal-insulator transition in intercalated bulk VSe$_{2}$
Ma, Wanru
Yang, Ye
Liang, Zuowei
Wu, Ping
Meng, Fanbao
Wang, Zhenyu
Chen, Xianhui
Materials Science
Mesoscale and Nanoscale Physics
Two-dimensional (2D) materials provide unique opportunities to realize emergent phenomena by reducing dimensionality. Using scanning tunneling microscopy combined with first-principles calculations, we determine an intriguing case of a metal-insulator transition (MIT) in a bulk compound, (TBA)$_{0.3}$VSe$_2$. Atomic-scale imaging reveals that the initial $4a_0 \times 4a_0$ charge density wave (CDW) order in 1T-VSe$_2$ transforms to $\sqrt{7}a_0 \times \sqrt{3}a_0$ ordering upon intercalation, which is associated with an insulating gap with a magnitude of up to approximately 115 meV. Our calculations reveal that this energy gap is highly tunable through electron doping introduced by the intercalant. Moreover, the robustness of the $\sqrt{7}a_0 \times \sqrt{3}a_0$ CDW order against the Lifshitz transition points to the key role of electron-phonon interactions in stabilizing the CDW state. Our work clarifies a rare example of a CDW-driven MIT in quasi-2D materials and establishes cation intercalation as an effective pathway for tuning both the dimensionality and the carrier concentration without inducing strain or disorder.
title Nanoscale determination of the metal-insulator transition in intercalated bulk VSe$_{2}$
topic Materials Science
Mesoscale and Nanoscale Physics
url https://arxiv.org/abs/2512.23264