Shi Jianping, Wang Xina, Zhang Shuai, Xiao Lingfeng, Huan Yahuan, Gong Yue, Zhang Zhepeng, Li Yuanchang, Zhou Xiebo, Hong Min, Fang Qiyi, Zhang Qing, Liu Xinfeng, Gu Lin, Liu Zhongfan, Zhang Yanfeng
Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing, 100871, China.
Center for Nanochemistry (CNC), Beijing Science and Engineering Center for Nanocarbons, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.
Nat Commun. 2017 Oct 16;8(1):958. doi: 10.1038/s41467-017-01089-z.
Two-dimensional metallic transition metal dichalcogenides are emerging as prototypes for uncovering fundamental physical phenomena, such as superconductivity and charge-density waves, as well as for engineering-related applications. However, the batch production of such envisioned transition metal dichalcogenides remains challenging, which has hindered the aforementioned explorations. Herein, we fabricate thickness-tunable tantalum disulfide flakes and centimetre-sized ultrathin films on an electrode material of gold foil via a facile chemical vapour deposition route. Through temperature-dependent Raman characterization, we observe the transition from nearly commensurate to commensurate charge-density wave phases with our ultrathin tantalum disulfide flakes. We have obtained high hydrogen evolution reaction efficiency with the as-grown tantalum disulfide flakes directly synthesized on gold foils comparable to traditional platinum catalysts. This work could promote further efforts for exploring new efficient catalysts in the large materials family of metallic transition metal dichalcogenides, as well as exploiting their applications towards more versatile applications.Metallic transition metal dichalcogenides are important materials for catalysis, but scalable and controllable preparation methods are scarce. Here, the authors synthesize 2H-TaS as centimetre-scale films of tunable thickness and show they are an efficient catalyst for hydrogen evolution.
二维金属过渡金属二硫属化物正在成为揭示诸如超导性和电荷密度波等基本物理现象以及工程相关应用的原型材料。然而,批量生产这种预想的过渡金属二硫属化物仍然具有挑战性,这阻碍了上述探索。在此,我们通过一种简便的化学气相沉积路线,在金箔电极材料上制备了厚度可调的二硫化钽薄片和厘米级超薄薄膜。通过与温度相关的拉曼表征,我们观察到我们的超薄二硫化钽薄片从近相称到相称的电荷密度波相的转变。我们直接在金箔上合成的生长态二硫化钽薄片获得了与传统铂催化剂相当的高析氢反应效率。这项工作可以推动在金属过渡金属二硫属化物这一大型材料家族中探索新型高效催化剂的进一步努力,以及开发它们在更多样化应用方面的应用。金属过渡金属二硫属化物是催化领域的重要材料,但可扩展且可控的制备方法稀缺。在此,作者合成了具有可调厚度的厘米级薄膜形式的2H-TaS,并表明它们是析氢的高效催化剂。