Quantum Confined Tomonaga-Luttinger Liquid in Mo<sub>6</sub>Se<sub>6</sub> Nanowires Converted from an Epitaxial MoSe<sub>2</sub> Monolayer.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32092277.
- Also identified by DOI 10.1021/acs.nanolett.0c00090.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Confining interacting particles in one-dimension (1D) changes the electronic behavior of the system fundamentally, which has been studied extensively in the past. Examples of 1D metallic systems include carbon nanotubes, quasi-1D organic conductors, metal chains, and domain boundary defects in monolayer thick transition-metal dichalcogenides such as MoSe<sub>2</sub>. Here single and bundles of Mo<sub>6</sub>Se<sub>6</sub> nanowires were fabricated through annealing a MoSe<sub>2</sub> monolayer grown by molecular-beam epitaxy on graphene. Conversion from two-dimensional (2D) MoSe<sub>2</sub> film to 1D Mo<sub>6</sub>Se<sub>6</sub> nanowire is reversible. Mo<sub>6</sub>Se<sub>6</sub> nanowires form preferentially at the Se-terminated zigzag edges of MoSe<sub>2</sub> and stitch to it via two distinct atomic configurations. The Mo<sub>6</sub>Se<sub>6</sub> wire is metallic and its length is tunable, which represents one of few 1D systems that exhibit properties pertinent to quantum confined Tomonaga-Luttinger liquid, as evidenced by scanning tunneling microscopic and spectroscopic studies.