Materials Science and Engineering, Rutgers University, 607 Taylor Road, Piscataway, New Jersey 08854, USA.
1] Department of Chemistry and Chemical Biology, Rutgers University, 610 Taylor Road, Piscataway, New Jersey 08854, USA [2] Department of Chemical and Biochemical Engineering, Rutgers University, 98 Brett Road, Piscataway, New Jersey 08854, USA.
Nat Chem. 2015 Jan;7(1):45-9. doi: 10.1038/nchem.2108. Epub 2014 Nov 10.
Chemical functionalization of low-dimensional materials such as nanotubes, nanowires and graphene leads to profound changes in their properties and is essential for solubilizing them in common solvents. Covalent attachment of functional groups is generally achieved at defect sites, which facilitate electron transfer. Here, we describe a simple and general method for covalent functionalization of two-dimensional transition metal dichalcogenide nanosheets (MoS₂, WS₂ and MoSe₂), which does not rely on defect engineering. The functionalization reaction is instead facilitated by electron transfer between the electron-rich metallic 1T phase and an organohalide reactant, resulting in functional groups that are covalently attached to the chalcogen atoms of the transition metal dichalcogenide. The attachment of functional groups leads to dramatic changes in the optoelectronic properties of the material. For example, we show that it renders the metallic 1T phase semiconducting, and gives it strong and tunable photoluminescence and gate modulation in field-effect transistors.
化学功能化的低维材料,如纳米管、纳米线和石墨烯,会导致它们的性质发生深刻的变化,这对于将它们溶解在常见溶剂中是必不可少的。官能团的共价附着通常在缺陷部位实现,这有利于电子转移。在这里,我们描述了一种简单而通用的方法,用于二维过渡金属二卤化物纳米片(MoS₂、WS₂和 MoSe₂)的共价功能化,该方法不依赖于缺陷工程。相反,功能化反应是通过富电子的 1T 相和有机卤化物反应物之间的电子转移来促进的,导致官能团与过渡金属二卤化物的硫属原子共价连接。官能团的附着导致材料的光电性质发生剧烈变化。例如,我们表明它使金属 1T 相半导体化,并赋予其在晶体管中强且可调谐的光致发光和栅极调制。