Ali Umar Akrajas, Md Saad Siti Khatijah, Mat Salleh Muhamad
Institute of Microengineering and Nanoelectronics, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Malaysia.
Department of Physics, Faculty of Mathematics and Natural Sciences, Universitas Andalas, Kampus Unand Limau Manis, 25163 Padang, Indonesia.
ACS Omega. 2017 Jul 10;2(7):3325-3332. doi: 10.1021/acsomega.7b00580. eCollection 2017 Jul 31.
Newly discovered two-dimensional (2D) atomic crystals (nanosheet) of platinum diselenide (PtSe) have progressively attracted attention due to their expected high performance in catalysis, sensing, electronics, and optoelectronics applications. Further extraordinary physicochemical properties are expected if these nanosheets of platinum diselenide can possess mesoporosity as this may enable a high range of molecular adsorption, enhancing their functionalities in catalysis, batteries, supercapacitors, and sensing. Here, we present for the first time a straightforward, aqueous-phase synthetic strategy for the preparation of scalable nanosheets of platinum diselenide with mesoporous structure via a surfactant-templated self-assembly followed by a thermal annealing phase-transformation process. We used hexamethylenetetramine as a hexagonal honeycomb (sp-sp orbital) scaffold for assembling the Pt and Se organic complexes to form the nanosheet structure, which is stable, preserving the 2D structure and mesoporosity during a thermal annealing at 500 °C. Density functional theory analysis then indicated that the mesoporous nanosheets of platinum diselenide exhibit a high free-energy and large density of π electrons crossing the Fermi level, inferring a high-catalytic performance. This effortless strategy is currently being extended to the synthesis of other transition metal dichalcogenides, including the preparation of multi-metal atomic dichalcogenide nanosheets, for a wide variety of scientific and technological applications.
新发现的二维(2D)二硒化铂(PtSe₂)原子晶体(纳米片)因其在催化、传感、电子和光电子应用中预期的高性能而逐渐受到关注。如果这些二硒化铂纳米片能够具有介孔结构,预计会展现出非凡的物理化学性质,因为这可能会实现高范围的分子吸附,增强它们在催化、电池、超级电容器和传感方面的功能。在此,我们首次展示了一种直接的水相合成策略,通过表面活性剂模板自组装,随后进行热退火相变过程,制备具有介孔结构的可扩展二硒化铂纳米片。我们使用六亚甲基四胺作为六边形蜂窝状(sp-sp轨道)支架来组装Pt和Se有机配合物,以形成纳米片结构,该结构在500℃热退火过程中稳定,保留了二维结构和介孔性。密度泛函理论分析表明,二硒化铂介孔纳米片表现出高自由能和跨越费米能级的大π电子密度,这意味着其具有高催化性能。这种简便的策略目前正在扩展到其他过渡金属二硫属化物的合成,包括制备多金属原子二硫属化物纳米片,以用于广泛的科学和技术应用。