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Tuning adhesion forces between functionalized gold colloidal nanoparticles and silicon AFM tips: role of ligands and capillary forces

机译:调节功能化的金胶体纳米颗粒和硅原子力显微镜针尖之间的粘附力:配体和毛细管力的作用

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摘要

Adhesion forces between functionalized gold colloidal nanoparticles (Au NPs) and scanning probe microscope silicon tips were experimentally investigated by atomic force microscopy (AFM) equipped with PeakForce QNM (Quantitative Nanoscale Mechanics) module. Au NPs were synthesized by a seed-mediated process and then functionalized with thiols containing different functional groups: amino, hydroxy, methoxy, carboxy, methyl, and thiol. Adhesion measurements showed strong differences between NPs and silicon tip depending on the nature of the tail functional group. The dependence of the adhesion on ligand density for different thiols with identical functional tail-group was also demonstrated. The calculated contribution of the van der Waals (vdW) forces between particles was in good agreement with experimentally measured adhesive values. In addition, the adhesion forces were evaluated between flat Au films functionalized with the same molecular components and silicon tips to exclude the effect of particle shape on the adhesion values. Although adhesion values on flat substrates were higher than on their nanoparticle counterparts, the dependance on functional groups remained the same.
机译:通过配备PeakForce QNM(定量纳米尺度力学)模块的原子力显微镜(AFM),对功能化的金胶体纳米颗粒(Au NPs)和扫描探针显微镜硅尖端之间的粘附力进行了实验研究。金纳米颗粒通过种子介导的方法合成,然后用含有不同官能团的巯基官能化:氨基,羟基,甲氧基,羧基,甲基和硫醇。粘合力测量结果表明,NPs和硅尖端之间的差异很大,具体取决于尾部官能团的性质。还证明了具有相同功能性尾基的不同硫醇的粘附力对配体密度的依赖性。颗粒之间的范德华力(vdW)的计算贡献与实验测得的粘合力值非常吻合。另外,在用相同分子组分官能化的平坦金膜和硅尖端之间评估了粘附力,以排除颗粒形状对粘附值的影响。尽管在平坦基材上的附着力值高于其在纳米基材上的附着力,但对官能团的依赖性保持不变。

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