Duan Yichen, Rani Sana, Zhang Yuying, Ni Chaoying, Newberg John T, Teplyakov Andrew V
Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
Department of Materials Science and Engineering, University of Delaware, Newark, Delaware 19716, United States.
J Phys Chem C Nanomater Interfaces. 2017 Apr 6;121(13):7240-7247. doi: 10.1021/acs.jpcc.6b12896. Epub 2017 Mar 13.
Trimethylphosphine(hexafluoroacetylacetonato)silver(I) was used as a precursor to deposit silver onto silicon surfaces. The deposition was performed on silicon-based substrates including silica, H-terminated Si(100), and OH-terminated (oxidized) Si(100). The deposition processes at room temperature and elevated temperature (350 °C) were compared. The successful deposition resulted in nanostructures or nanostructured films as confirmed by atomic force microscopy (AFM) and scanning electron microscopy (SEM) with metallic silver being the majority deposited species as confirmed by X-ray photoelectron spectroscopy (XPS). The reactivity of the precursor depends drastically not only on the temperature of the process but also on the type of substrate. Density functional theory (DFT) was used to explain these differences and to propose the mechanisms for the initial deposition steps.
三甲基膦(六氟乙酰丙酮)银(I)被用作在硅表面沉积银的前驱体。沉积过程在包括二氧化硅、氢终止的Si(100)和羟基终止(氧化)的Si(100)在内的硅基衬底上进行。比较了室温及高温(350°C)下的沉积过程。通过原子力显微镜(AFM)和扫描电子显微镜(SEM)确认成功沉积得到了纳米结构或纳米结构薄膜,通过X射线光电子能谱(XPS)确认大部分沉积物种为金属银。前驱体的反应活性不仅极大地取决于过程温度,还取决于衬底类型。采用密度泛函理论(DFT)来解释这些差异并提出初始沉积步骤的机制。