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Assessing Pair Interaction Potentials of Nanoparticles on Liquid Interfaces

机译:评估纳米颗粒对液体界面的对相互作用电位

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The pair interaction potentials of polymer-grafted silica nanoparticles (NPs) at liquid surfaces were determined by scanning electron microscopy, exploiting the nonvolatility of ionic liquids to stabilize the specimens against microscope vacuum. Even at near contact, individual, two-dimensionally well-dispersed NPs were resolved. The potential of mean force, reduced to the pair interaction potential for dilute NPs, was extracted with good accuracy from the radial distribution function, as both NP diameter and grafted polymer chain length were varied. While NP polydispersity somewhat broadened the core repulsion, the pair potential well-approximated a hard sphere interaction, making these systems suitable for model studies of interfacially bound NPs. For short (5 kDa) poly(ethylene glycol) ligands, a weak (
机译:通过扫描电子显微镜测定聚合物接枝二氧化硅纳米颗粒(NPS)的对相互作用电位(NPS),利用离子液体的非易失性来稳定对显微镜真空的非易失性。即使在接近接触时,也可以解决个体,二维分散的NPS。从径向分布函数的良好精度提取到稀释NP的对相互作用电位的平均力的潜力,随着NP直径和接枝的聚合物链长度的变化。虽然NP多分散性稍微拓宽了核心排斥,但这对势率近似的硬球相互作用,使这些系统适用于界面结合的NPS的模型研究。对于短(5kDa)聚(乙二醇)配体,辨别出弱(

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