扫描隧道显微镜
拉曼光谱
共价键
基质(水族馆)
纳米结构
材料科学
卟啉
纳米技术
制作
表面增强拉曼光谱
分子
自组装
光谱学
化学物理
化学
拉曼散射
光化学
光学
有机化学
地质学
病理
物理
海洋学
替代医学
医学
量子力学
作者
Jeremy F. Schultz,Linfei Li,Sayantan Mahapatra,Nan Jiang
标识
DOI:10.1088/1361-648x/ac57d8
摘要
Surface-bound reactions have become a viable method to develop nanoarchitectures through bottom-up assembly with near atomic precision. However, the bottom-up fabrication of nanostructures on surfaces requires careful consideration of the intrinsic properties of the precursors and substrate as well as the complex interplay of any interactions that arise in the heterogeneous two-dimensional (2D) system. Therefore, it becomes necessary to consider these systems with characterization methods sensitive to such properties with suitable spatial resolution. Here, low temperature ultrahigh vacuum scanning tunneling microscopy (STM) and tip-enhanced Raman spectroscopy (TERS) were used to investigate the formation of 2D covalent networks via coupling reactions of tetra(4-bromophenyl)porphyrin (Br4TPP) molecules on a Ag(100) substrate. Through the combination of STM topographic imaging and TERS vibrational fingerprints, the conformation of molecular precursors on the substrate was understood. Following the thermally activated coupling reaction, STM and TERS imaging confirm the covalent nature of the 2D networks and suggest that the apparent disorder arises from molecular flexibility.
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