Department of Materials, Imperial College London, London, SW7 2AZ, UK.
Nat Commun. 2019 Feb 12;10(1):712. doi: 10.1038/s41467-019-08594-3.
Crystal phase control in layered transition metal dichalcogenides is central for exploiting their different electronic properties. Access to metastable crystal phases is limited as their direct synthesis is challenging, restricting the spectrum of reachable materials. Here, we demonstrate the solution phase synthesis of the metastable distorted octahedrally coordinated structure (1T' phase) of WSe nanosheets. We design a kinetically-controlled regime of colloidal synthesis to enable the formation of the metastable phase. 1T' WSe branched few-layered nanosheets are produced in high yield and in a reproducible and controlled manner. The 1T' phase is fully convertible into the semiconducting 2H phase upon thermal annealing at 400 °C. The 1T' WSe nanosheets demonstrate a metallic nature exhibited by an enhanced electrocatalytic activity for hydrogen evolution reaction as compared to the 2H WSe nanosheets and comparable to other 1T' phases. This synthesis design can potentially be extended to different materials providing direct access of metastable phases.
层状过渡金属二卤族化合物的晶体相控制对于开发其不同的电子性质至关重要。由于其直接合成具有挑战性,因此获得亚稳晶体相的途径受到限制,从而限制了可达到的材料范围。在这里,我们展示了通过溶液相合成 WSe 纳米片的亚稳扭曲八面体配位结构(1T'相)。我们设计了一种动力学控制的胶体合成方案,以实现亚稳相的形成。以高产率和可重复且可控的方式制备了 1T' WSe 支化少层纳米片。在 400°C 下进行热退火时,1T'相完全可转化为半导体 2H 相。与 2H WSe 纳米片相比,1T' WSe 纳米片表现出金属性质,其析氢反应的电催化活性更高,与其他 1T'相相当。这种合成设计有可能扩展到不同的材料,为亚稳相的直接获得提供了可能。