Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Fukuoka 816-8580, Japan.
Phys Chem Chem Phys. 2018 Dec 5;20(47):29790-29797. doi: 10.1039/c8cp04418j.
Recently, transition metal dichalcogenides (TMDCs) have attracted great interest due to their unique electronic and optical properties. Chemical vapor deposition (CVD) has been regarded as the most promising method for the synthesis of large-area TMDCs with high reproducibility. Having similar hexagonal crystal structures with many TMDCs, c-plane sapphire is commonly used as a growth substrate in CVD. However, few studies have been reported on the influence of the sapphire substrate on the growth behavior and physical properties of TMDCs. In this work, we demonstrate that higher strain is induced in epitaxially grown WS2 grains via van der Waals interactions with sapphire as compared with misaligned WS2 grains. In addition, this strain was found to enhance overlayer deposition on monolayer WS2, while multilayer growth was not observed in non-epitaxial WS2. Photoluminescence (PL) of the epitaxially grown WS2 grains was reduced, reflecting the effective van der Waals interaction with sapphire. Moreover, low-temperature PL measurements revealed strong influence of the c-plane sapphire surface on the optical properties of WS2. Density functional theory (DFT) calculation supports that the aligned WS2 grains are more strongly bound to the sapphire surface, as compared with misaligned WS2. Our work offers a new insight into the understanding of the influence of the substrate on the CVD-grown TMDC materials.
最近,由于过渡金属二卤化物(TMDCs)具有独特的电子和光学特性,因此引起了极大的兴趣。化学气相沉积(CVD)被认为是合成大面积 TMDCs 的最有前途的方法,具有高重复性。具有与许多 TMDCs 相似的六方晶体结构,c 面蓝宝石通常用作 CVD 中的生长衬底。然而,关于蓝宝石衬底对 TMDCs 生长行为和物理性质的影响的研究很少。在这项工作中,我们证明了与未对准的 WS2 晶粒相比,通过范德华相互作用与蓝宝石外延生长的 WS2 晶粒中诱导了更高的应变。此外,发现这种应变增强了在单层 WS2 上的覆盖层沉积,而在非外延 WS2 中未观察到多层生长。外延生长的 WS2 晶粒的光致发光(PL)减少,反映了与蓝宝石的有效范德华相互作用。此外,低温 PL 测量揭示了 c 面蓝宝石表面对 WS2 光学性质的强烈影响。密度泛函理论(DFT)计算支持与未对准的 WS2 相比,对准的 WS2 晶粒与蓝宝石表面的结合更强。我们的工作为理解衬底对 CVD 生长的 TMDC 材料的影响提供了新的见解。