Department of Chemistry, Korea University, Jochiwon 339-700, Republic of Korea.
Nanoscale. 2018 Jun 21;10(24):11349-11356. doi: 10.1039/c8nr02365d.
The novel properties of two-dimensional materials have motivated extensive studies focused on transition metal dichalcogenides (TMDs), which led to many interesting findings in recent years. Further advances in this area would require the development of effective methods for producing nanostructured TMDs with a controlled structure. Herein, we report unique MoS2 layered nanostructures intercalated with dimethyl-p-phenylenediamine (DMPD) with various concentrations, synthesized by a one-step hydrothermal reaction. The MoS2 layers possess a significantly expanded interlayer spacing. Remarkably, as the concentration of DMPD increases, the MoS2 preferentially adopts a unique metallic 1T' (distorted 1T) phase. The intercalated MoS2 exhibits excellent catalytic performance in the hydrogen evolution reaction. First-principles calculations show that the phase transition from 2H to 1T' phase occurs with increasing concentrations of DMPD, which can be accelerated by the S vacancies. A significant charge transfer from the DMPD molecules to MoS2 stabilizes the 1T' over the 2H phase, driving the 2H-1T' phase conversion. The DMPD and the S vacancies increased the carrier concentration, which leads to the enhanced catalytic performance. The present work illustrates how the phase control of TMDs can be effectively achieved by the intercalation of electron-donating molecules.
二维材料的新奇性质激发了人们对过渡金属二卤化物(TMDs)的广泛研究,近年来取得了许多有趣的发现。该领域的进一步进展需要开发有效方法来制备具有可控结构的纳米结构化 TMDs。在此,我们报告了一种独特的 MoS2 层状纳米结构,其通过一步水热反应合成,其中插层有不同浓度的二甲基对苯二胺(DMPD)。MoS2 层具有显著扩展的层间距。值得注意的是,随着 DMPD 浓度的增加,MoS2 优先采用独特的金属 1T'(扭曲 1T)相。插层 MoS2 在析氢反应中表现出优异的催化性能。第一性原理计算表明,随着 DMPD 浓度的增加,从 2H 相向 1T'相的转变可以通过 S 空位加速。来自 DMPD 分子的显著电荷转移将 MoS2 稳定在 1T'相中,从而驱动 2H-1T'相的转变。DMPD 和 S 空位增加了载流子浓度,从而提高了催化性能。本工作说明了如何通过电子供体分子的插层来有效控制 TMDs 的相。