Related Experiment Video
Updated: Apr 15, 2026

Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication
Published on: November 28, 2017
Topotactic Conversion to High-Valent Metastable 2D Semimetallic W2N3 via Lateral Anion Exchange of Bilayer WS2
Jeong-Hwan Park1,2, Je Oh Choi1,2, Hyo Gyeong Shin2
1Center for Van der Waals Quantum Solids, Institute for Basic Science, Pohang 37673, Republic of Korea.
Abstract:
Phase control in the vapor-phase growth of transition metal nitrides is typically restricted by substantial kinetic barriers during precursor dissociation and an inherent thermodynamic instability towards nitrogen loss. Consequently, extreme growth conditions such as high pressure or plasma environments are often required. Here, we circumvent these limitations to stabilize high-valent, metastable 2D semimetallic tungsten nitride (W2N3) by employing a tailored topotactic conversion of a bilayer WS2 van der Waals template. In particular, we preserve the structural symmetry and stacking order of the W metal sublattice, while leveraging thermodynamic control to suppress vacancy aggregation, enabling homogeneous and synchronous nitrogen substitution across the layers. This uniform transformation facilitates "hyper-stoichiometric" nitrogen incorporation, inducing subtle structural distortions to trigger the electronic phase transition from a semiconductor to a semimetal. Beyond W2N3, our approach provides a universal route to synthesize nitrogen-rich, nonequilibrium 2D semimetallic nitrides from the broader family of transition metal dichalcogenides, advancing the development of functional 2D material engineering.
Related Concept Videos
Valence Bond Theory
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than...

