Electrostatic Interaction between Nonuniformly Charged Colloids: Experimental and Numerical Study

被引:1
|
作者
Derot, Claire [1 ]
Porcar, Lionel [2 ]
Lee, YongJin [3 ,4 ]
Pincus, Phillip A. [5 ,6 ]
Jho, YongSeok [4 ,5 ,6 ]
In, Martin [1 ]
机构
[1] Univ Montpellier, UMR CNRS 5221, Lab Charles Coulomb L2C, F-34059 Montpellier, France
[2] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[3] Asia Pacific Ctr Theoret Phys, Pohang 790784, Gyeongbuk, South Korea
[4] Pohang Univ Sci & Technol, Dept Phys, Pohang 790784, Gyeongbuk, South Korea
[5] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[6] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
基金
新加坡国家研究基金会;
关键词
DOUBLE-LAYER FORCES; POISSON-BOLTZMANN; LATEX-PARTICLES; SURFACES; MICROEMULSION; COUNTERIONS; ATTRACTION; AGGREGATION; RENORMALIZATION; ELECTROLYTES;
D O I
10.1021/la504579c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The influence of the surface charge distribution on the interaction between nanosized particles in water is reported. The distribution of charges at the surface of initially neutral microemulsion droplets has been modulated by additions of various oligomeric cationic surfactants. The osmotic compressibility of the doped microemulsions was measured by light and small-angle neutrons scattering and reveals that the overall effective interaction induced by the ionic groups is repulsive. However, particular charge distributions decrease the osmotic compressibility much less than others. Independent measurements of the activity of the bromide counterions with specific electrodes evidence a significant decrease in the effective charge, which, however, cannot account for the osmotic compressibility in the framework of the primitive model. The q dependence of the structure factor reveals an attractive contribution over a short distance. Numerical studies assign this attractive contribution to the overlap of hydration shells that are extended as a result of the charge localization.
引用
收藏
页码:1649 / 1659
页数:11
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