TY - JOUR
T1 - Two-Dimensional van der Waals Polar Metal MoOBr2
AU - Sun, Xuzhou
AU - Ye, Fengfeng
AU - Fang, Yuqiang
AU - Wang, Jiapeng
AU - Xu, Lixuan
AU - Lin, Yongliang
AU - Li, Yiwei
AU - Lu, Ruize
AU - Li, Zhiqin
AU - Li, Hui
AU - Gou, Gaoyang
AU - Li, Yang
AU - Huang, Fuqiang
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/7/22
Y1 - 2026/7/22
N2 - Two-dimensional (2D) van der Waals (vdW) polar metals, which integrate long-range polar order and metallic conductivity, have garnered enormous interest for their extraordinary properties, including non-reciprocal charge transport and nonlinear optical effects. However, intrinsic 2D vdW polar metals remain exceedingly rare, as the dense itinerant electrons strongly screen internal electric fields and destabilize the macroscopic polarization needed for polar order. Herein, we report the discovery of MoOBr2, the first 2D vdW polar metal stacked by polar atomic layers. Single-crystal X-ray diffraction and atomic-resolution scanning transmission electron microscopy reveal that MoOBr2 crystallizes in the non-centrosymmetric space group C2, with polarity originating from asymmetric [MoO2Br4] octahedral distortions. Angle-resolved photoemission spectroscopy and electrical transport measurements confirm its metallic behavior with a room-temperature resistivity of 5.13 × 10–5 Ω m and a carrier concentration of 1.34 × 1020 cm–3. The broken spatial inversion symmetry of MoOBr2 was further demonstrated by both second-harmonic generation and second-order nonlinear electrical transport measurement, providing the complementary signatures of the polar metallic state. Remarkably, MoOBr2 exhibits a high thermal conductivity of 219 W m–1 K–1, enabling efficient heat dissipation in high-power-density nanoscale devices. This work not only benefits next-generation multifunctional spintronic and nonlinear optoelectronic applications but also offers a rational chemical design strategy for new polar metals.
AB - Two-dimensional (2D) van der Waals (vdW) polar metals, which integrate long-range polar order and metallic conductivity, have garnered enormous interest for their extraordinary properties, including non-reciprocal charge transport and nonlinear optical effects. However, intrinsic 2D vdW polar metals remain exceedingly rare, as the dense itinerant electrons strongly screen internal electric fields and destabilize the macroscopic polarization needed for polar order. Herein, we report the discovery of MoOBr2, the first 2D vdW polar metal stacked by polar atomic layers. Single-crystal X-ray diffraction and atomic-resolution scanning transmission electron microscopy reveal that MoOBr2 crystallizes in the non-centrosymmetric space group C2, with polarity originating from asymmetric [MoO2Br4] octahedral distortions. Angle-resolved photoemission spectroscopy and electrical transport measurements confirm its metallic behavior with a room-temperature resistivity of 5.13 × 10–5 Ω m and a carrier concentration of 1.34 × 1020 cm–3. The broken spatial inversion symmetry of MoOBr2 was further demonstrated by both second-harmonic generation and second-order nonlinear electrical transport measurement, providing the complementary signatures of the polar metallic state. Remarkably, MoOBr2 exhibits a high thermal conductivity of 219 W m–1 K–1, enabling efficient heat dissipation in high-power-density nanoscale devices. This work not only benefits next-generation multifunctional spintronic and nonlinear optoelectronic applications but also offers a rational chemical design strategy for new polar metals.
UR - https://www.scopus.com/pages/publications/105045588824
U2 - 10.1021/jacs.6c08223
DO - 10.1021/jacs.6c08223
M3 - 文章
C2 - 42406431
AN - SCOPUS:105045588824
SN - 0002-7863
VL - 148
SP - 30278
EP - 30286
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 28
ER -