Experimental Determination of Particle Size-Dependent Surface Charge Density for Silica Nanospheres

被引:35
|
作者
Shi, Ya-Rong [1 ,2 ]
Ye, Man-Ping [2 ]
Du, Lu-Chao [1 ]
Weng, Yu-Xiang [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, CAS Key Lab Soft Matter Phys, Beijing 100190, Peoples R China
[2] China Jiliang Univ, Coll Opt & Elect Technol, Hangzhou 310018, Zhejiang, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
SPHERICAL COLLOIDAL PARTICLE; ELECTROPHORETIC MOBILITY; ANALYTIC EXPRESSIONS; OXIDE NANOPARTICLES; INTERFACE; CARRIERS; MODEL; LAYER; FUNCTIONALITY; CONSTANTS;
D O I
10.1021/acs.jpcc.8b07566
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Surface charge densities of spherical silica nanoparticles of varied size spanning from 4.1 to 495.7 nm in NaCl solution with a concentration from 0.003 to 1.2 mM at a pH value of 8.0 were determined by converting their corresponding measured zeta potential with Poisson-Boltzmann model. The magnitude of the derived surface charge density (negative) at a given NaCl concentration of 0.225 mM decreases monotonically with the increasing particle size and reaches almost a steady value when the size exceeds 30 nm, revealing clearly the effect of the nanoparticle curvature on the surface charge density. The experimental data provide a consensus for the validity of different models describing the relation between the surface charge density and the electric potential, that is, the surface complexation model and the Poisson-Boltzmann model for the charged nanospheres in electrolyte solution. We found that if the former includes the curvature-dependent deprotonation constant of the surface silanol groups, both models would give a consistent result.
引用
收藏
页码:23764 / 23771
页数:8
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