Observation of a Novel Charge Density Wave Superstructure in Monolayer 1T-VS2 at Room Temperature and its Evolution in Multilayers
Abstract
Spontaneous formation of charge density wave (CDW) superstructures in monolayers (MLs) of a two-dimensional (2D) crystal lattice is fundamental in understanding its complex quantum states. We report a successful top-down liquid phase exfoliation and stamp transfer process (LPESTP) to create ML VS2, undergoing a CDW transition at room temperature. Using high-resolution transmission electron microscopy (HRTEM) and electron diffraction (ED), we observed the coexistence of 1T and 2H polymorphic phases in VS2 at room temperature, and only the 1T phase undergoes CDW transition. We discovered a novel incommensurate CDW superstructure (7 × 7) R19.1o in ML 1T-VS2. With an increase in the number of layers, the CDW order changes to a commensurate (2 × 2× 1) superstructure. Using angle-dependent photoelectron spectroscopy and TEM, we have shown that vanadium atoms self-intercalate as V3+ ions in multilayer VS2 and are responsible for the evolution of the CDW superstructure from the incommensurate (7 × 7) R 19.1o to the commensurate (2×2×1) order. We also report the observation of novel Moir\'e superlattices in twisted bilayer 1T-VS2 flakes with trapped CDW superstructure of the monolayer. The density functional theory (DFT) calculation performed on ML 1T-VS2 show that the observed (7 × 7) R 19.1o CDW superstructure has lower energy compared to that of the pristine undistorted ML and the CDW instability is driven by formation of strong soft-phonon modes. Our findings provide an important platform for understanding the evolution of CDW superstructures in 1T-VS2 with layer numbers and V self-intercalation.
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