Bulk 1T-NbSe2 Superconductor Stabilized by the Doped Ti-3d0 Electronic Configuration

Abstract Metastable 1T-phase transition-metal dichalcogenides host rich strongly correlated electronic phenomena, yet the synthesis of bulk 1T-NbSe2 remains a challenge. This difficulty stems from the energetic penalty associated with the octahedral coordination of Nb4+, whose 4d1 electronic configuration drives the 1T phase to relax into the thermodynamically stable 2H phase. Herein, we successfully synthesized 1T-Nb0.92Ti0.08Se2 crystals through a chemical vapor transport method. The intralayer Ti atoms induce the Nb4+ d-electron configuration to favor octahedral coordination, while a minority of intercalated Ti covalently pins the 1T layers. Angle-resolved photoemission spectroscopy reveals an intact metallic Fermi surface and a narrow band near the Fermi level, indicating the suppression of charge-density-wave reconstruction and an enhanced density of electronic states. In contrast to the Mott-insulating monolayer 1T NbSe2, bulk 1T-Nb0.92Ti0.08Se2 exhibits robust type-II superconductivity with a transition temperature of 7.2 K and an in-plane upper critical field of 13.46 T, exceeding the Pauli paramagnetic limit. Furthermore, angle-dependent magnetotransport shows an anomalous 4-fold in-plane superconducting anisotropy that is unexpected for a trigonal lattice. This work establishes heteroatom doping as a powerful strategy for unlocking metastable 1T polymorphs, providing a highly versatile platform for exploring quantum physics.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-09-25
DOI
https://doi.org/10.1021/jacs.6c14384
Primary Topic
2D Materials and Applications
Type
article
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article

Bulk 1T-NbSe2 Superconductor Stabilized by the Doped Ti-3d0 Electronic Configuration

Fuqiang Huang, Xueyang Tu, Linchen Zhou, Yifan Zhou et al.
Journal of the American Chemical Society
2D Materials and Applications
article

Bulk 1T-NbSe2 Superconductor Stabilized by the Doped Ti-3d0 Electronic Configuration

Fuqiang Huang, Xueyang Tu, Linchen Zhou, Yifan Zhou, Yiwei Li, Xuzhou Sun, Yuqiang Fang, Zhongxun Tian, Hui Bi, Wei Zhao, Kunqi Li
article en

Abstract

Abstract Metastable 1T-phase transition-metal dichalcogenides host rich strongly correlated electronic phenomena, yet the synthesis of bulk 1T-NbSe2 remains a challenge. This difficulty stems from the energetic penalty associated with the octahedral coordination of Nb4+, whose 4d1 electronic configuration drives the 1T phase to relax into the thermodynamically stable 2H phase. Herein, we successfully synthesized 1T-Nb0.92Ti0.08Se2 crystals through a chemical vapor transport method. The intralayer Ti atoms induce the Nb4+ d-electron configuration to favor octahedral coordination, while a minority of intercalated Ti covalently pins the 1T layers. Angle-resolved photoemission spectroscopy reveals an intact metallic Fermi surface and a narrow band near the Fermi level, indicating the suppression of charge-density-wave reconstruction and an enhanced density of electronic states. In contrast to the Mott-insulating monolayer 1T NbSe2, bulk 1T-Nb0.92Ti0.08Se2 exhibits robust type-II superconductivity with a transition temperature of 7.2 K and an in-plane upper critical field of 13.46 T, exceeding the Pauli paramagnetic limit. Furthermore, angle-dependent magnetotransport shows an anomalous 4-fold in-plane superconducting anisotropy that is unexpected for a trigonal lattice. This work establishes heteroatom doping as a powerful strategy for unlocking metastable 1T polymorphs, providing a highly versatile platform for exploring quantum physics.

Journal of the American Chemical Society
Shanghai Jiao Tong University (CN), Wuhan University (CN), Shanghai Institute of Ceramics (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 26%
2D Materials and Applications
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Bulk 1T-NbSe2 Superconductor Stabilized by the Doped Ti-3d0 Electronic Configuration — Fuqiang Huang, Xueyang Tu, et al. · Journal of the American Chemical Society (2026) | TGRS Research Map | TGRS