Yoo GunWoo, Mo TaeJoon, Kim Yong-Sung, Choi Chang-Won, Moon Gunho, Lee Sumin, Hwang Chan-Cuk, Lee Woo-Ju, Choi Min-Yeong, Choi Jongyun, Choi Si-Young, Jo Moon-Ho, Kim Cheol-Joo
Center for Epitaxial van der Waals Quantum Solids, Institute for Basic Science (IBS), Pohang 37673, Republic of Korea.
Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
ACS Nano. 2025 Aug 12;19(31):28491-28501. doi: 10.1021/acsnano.5c07577. Epub 2025 Jul 29.
van der Waals (vdW) crystals are prone to twisting, sliding, and buckling due to inherently weak interlayer interactions. While thickness-controlled vdW structures have attracted considerable attention as ultrathin semiconducting channels, the deterministic synthesis of stacking-fault-free multilayers remains a persistent challenge. Here, we report the epitaxial growth of single-crystalline hexagonal bilayer MoS, enabled by the incorporation of Mo interstitials between layers during layer-by-layer deposition. The resulting bilayers exhibit exceptional structural robustness, maintaining their crystallinity and suppressing both rotational and translational interlayer misalignments even after transfer processes. Atomic-resolution analysis reveals that the Mo interstitials are located at a single sublattice site within the hexagonal lattice, where they form tetrahedral bonds with sulfur atoms from both MoS layers, effectively anchoring the interlayer registry. Density functional theory calculations further indicate that these Mo atoms act as nucleation centers, promoting the selective formation of the hexagonal bilayer phase. This approach offers a robust strategy for the deterministic growth of multilayer vdW crystals with precisely controlled stacking order and enhanced interlayer coupling.