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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Analysis of adsorption and binding behaviors of silver nanoparticles onto a pyridyl-terminated surface using XPS and AFM
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Analysis of adsorption and binding behaviors of silver nanoparticles onto a pyridyl-terminated surface using XPS and AFM

机译:使用XPS和AFM分析银纳米颗粒在吡啶基末端表面的吸附和结合行为

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In this study, we analyzed adsorption and binding behaviors of citrate-capped silver nanoparticles (AgNPs) on a pyridyl-terminated surface using X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Adsorption of the AgNPs onto the pyridyl-terminated silicon wafer surface was completed through pH-controlled sol immersion. The adsorption occurred predominantly at a pH less than the pK_b value of the pyridyl group and more than the pK_(a1) of citric acid, indicating that the driving force behind adsorption was electrostatic interaction. Adsorption of citrate onto the pyridyl group also occurred at pK_(a1) < pH < pK _b without AgNPs. According to XPS in the N1s region, larger deprotonation from the pyridinium-formed pyridyl groups was demonstrated subsequent to adsorption of the AgNPs. The deprotonation from the pyridinium indicates the formation of the neutral pyridyl group as the counterpart of hydrogen bonding with the carboxyl group of citrate. The binding state between the pyridyl group and citrate surrounding AgNPs is expected to be kept stable through hydrogen bonding and van der Waals force derived from the AgNPs approach to the pyridyl surface.
机译:在这项研究中,我们使用X射线光电子能谱(XPS)和原子力显微镜(AFM)分析了柠檬酸封端的银纳米颗粒(AgNPs)在吡啶基封端的表面上的吸附和结合行为。通过控制pH值的溶胶浸没法将AgNPs吸附到吡啶基封端的硅片表面上。吸附主要在小于吡啶基的pK_b值和大于柠檬酸的pK_(a1)的pH值下发生,表明吸附背后的驱动力是静电相互作用。在没有AgNP的情况下,柠檬酸在吡啶基上的吸附也发生在pK_(a1)H K_b。根据N1s区域的XPS,在吸附AgNP之后,证明了吡啶鎓形成的吡啶基具有更大的去质子作用。吡啶鎓的去质子化表明形成中性吡啶基,作为氢与柠檬酸盐的羧基键合的对应物。吡啶基与周围AgNPs的柠檬酸盐之间的结合状态有望通过氢键和源自AgNPs的吡啶基表面的范德华力保持稳定。

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