Bottom-up Synthesis of Highly Chiral 1T Molybdenum Disulfide Nanosheets

Chirality in inorganic nanostructures has recently stimulated the attention of many researchers, both to unravel fundamental questions on the origin of chirality in inorganic and hybrid materials, as well as to introduce novel promising properties that are originated by the symmetry breaking. MoS2 is one of the most investigated among the large family of layered transition metal dichalcogenides. In particular, the metastable metallic 1T-MoS2 phase is of large interest for potential applications. However, due to thermodynamic reasons, the synthesis of 1T-MoS2 phase is quite challenging. Herein, we present the first synthesis of chiral 1T-MoS2 phase which shows remarkably high chiroptical activity with a g-factor up to 0.01. Chiral 1T-MoS2 was produced using tartaric acid as a chiral ligand to induce symmetry breaking during the material's growth under hydrothermal conditions, leading to the formation of distorted hierarchical nanosheet assemblies exhibiting chiral morphology. Thorough optimization of the synthetic conditions was carried out to maximize chiroptical activity, which is strongly related to the nanostructures' morphology. Finally, the formation mechanism of the chiral 1T-MoS2 nanosheet assemblies was investigated, focusing on the role of molecular intermediates in the growth of the nanosheets and the transfer of chirality. Chiral 1T-MoS2 nanosheets were produced via hydrothermal synthesis in the presence of tartaric acid as a chiral ligand to control mirror symmetry breaking. This novel chiral inorganic nanomaterial exhibits a chiral morphology as well as remarkably high chiroptical activity, with a g-factor of up to 0.01. The optimization of the synthetic conditions and the material's formation mechanism revealed critical details on the transfer of chirality. image