电解质
反离子
纳米颗粒
分子动力学
溶剂化
化学物理
平均力势
表面电荷
吸附
偶极子
水溶液
无定形固体
分子
化学
溶剂化壳
化学工程
双层(生物学)
静电学
材料科学
计算化学
物理化学
离子
纳米技术
图层(电子)
结晶学
有机化学
工程类
电极
作者
Samantha Jenkins,Steven R. Kirk,Michael Persson,J. Carlen,Zareen Abbas
摘要
Explicit molecular dynamics simulations were applied to a pair of amorphous silica nanoparticles in aqueous solution, with diameter of 4.4 nm and with four different background electrolyte concentrations, to extract the mean force acting between the two silica nanoparticles. Dependences of the interparticle forces on the separation and the background electrolyte concentration were demonstrated. The nature of the interaction of the counterions with charged silica surface sites (deprotonated silanols) was investigated. A "patchy" double layer of adsorbed sodium counterions was observed. Dependences of the interparticle potential of mean force on the separation and the background electrolyte concentration were demonstrated. Direct evidence of the solvation forces is presented in terms of changes of the water ordering at the surfaces of the isolated and double nanoparticles. The nature of the interaction of the counterions with charged silica surface sites (deprotonated silanols) was investigated in terms of quantifying the effects of the number of water molecules separately inside each pair of nanoparticles by defining an impermeability measure. A direct correlation was found between the impermeability (related to the silica surface "hairiness") and the disruption of water ordering. Differences in the impermeability between the two nanoparticles are attributed to differences in the calculated electric dipole moment.
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