Bi Liya, Wang Yufei, Wang Zhe, Do Alexandria, Fuqua Alexander, Balto Krista P, Zhang Yanning, Figueroa Joshua S, Pascal Tod A, Tao Andrea R, Li Shaowei
Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0309, United States.
Program in Materials Science and Engineering, University of California, San Diego, La Jolla, California 92093-0418, United States.
Nano Lett. 2025 Feb 5;25(5):2027-2033. doi: 10.1021/acs.nanolett.4c05885. Epub 2025 Jan 23.
The structural and chemical properties of metal nanoparticles are often dictated by their interactions with molecular ligand shells. These interactions are highly material-specific and can vary significantly even among elements within the same group or materials with similar crystal structure. In this study, we surveyed the heterogeneous interactions between an -terphenyl isocyanide ligand and Au and Ag nanoparticles (NPs) at the single-molecule limit. Specifically, we found that the ligation behavior with this molecule differs significantly between that of Au and AgNPs. Surface-enhanced Raman spectroscopy measurements revealed unique enhancement factors for two molecular vibrational modes between two metal surfaces, indicating different ligand binding geometries. Molecular-level characterization using scanning tunneling microscopy allowed us to directly visualize these variations between Ag and Au surfaces, which we assign as two distinct binding mechanisms. This molecular-scale visualization provides clear insights into the different ligand-metal interactions as well as the chemical behavior and spectroscopic characteristics of isocyanide-functionalized NPs.
金属纳米粒子的结构和化学性质通常由它们与分子配体壳层的相互作用决定。这些相互作用具有高度的材料特异性,即使在同一族元素或具有相似晶体结构的材料之间也可能有显著差异。在本研究中,我们在单分子极限下研究了对三联苯异腈配体与金和银纳米粒子(NPs)之间的异质相互作用。具体而言,我们发现该分子与金和银纳米粒子的连接行为存在显著差异。表面增强拉曼光谱测量揭示了两种金属表面上两种分子振动模式的独特增强因子,表明配体结合几何结构不同。使用扫描隧道显微镜进行的分子水平表征使我们能够直接观察到银和金表面之间的这些差异,我们将其归因于两种不同的结合机制。这种分子尺度的可视化提供了对不同配体 - 金属相互作用以及异腈功能化纳米粒子的化学行为和光谱特征的清晰见解。