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| Autori principali: | , , , , , , |
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| Natura: | Preprint |
| Pubblicazione: |
2025
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| Soggetti: | |
| Accesso online: | https://arxiv.org/abs/2512.23264 |
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| _version_ | 1866918265288130560 |
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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 |