Surface-dependent chemical equilibrium constants and capacitances for bare and 3-cyanopropyldimethylchlorosilane coated silica nanochannels

被引:45
作者
Andersen, Mathias Baekbo [1 ]
Frey, Jared [2 ]
Pennathur, Sumita [2 ]
Bruus, Henrik [1 ]
机构
[1] Tech Univ Denmark, Dept Micro & Nanotechnol, DK-2800 Lyngby, Denmark
[2] Univ Calif Santa Barbara, Dept Mech Engn, Santa Barbara, CA 93106 USA
关键词
Nanofluidics; Gouy-Chapman-Stern triple-layer model; Silica nanochannels; Cyanosilane surface coating; Capillary filling; CHARGE REGULATION MODEL; OXIDE-WATER INTERFACE; ELECTROKINETIC TRANSPORT; ADSORPTION; COMPLEXATION; FLUORESCEIN; IONS; IONIZATION; PRINCIPLES; GLASS;
D O I
10.1016/j.jcis.2010.09.025
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
We present a combined theoretical and experimental analysis of the solid-liquid interface of fused-silica nanofabricated channels with and without a hydrophilic 3-cyanopropyldimethylchlorosilane (cyanosilane) coating. We develop a model that relaxes the assumption that the surface parameters C-1, C-2, and pK(+) are constant and independent of surface composition. Our theoretical model consists of three parts: (i) a chemical equilibrium model of the bare or coated wall, (ii) a chemical equilibrium model of the buffered bulk electrolyte, and (iii) a self-consistent Gouy-Chapman-Stern triple-layer model of the electro-chemical double layer coupling these two equilibrium models. To validate our model, we used both pH-sensitive dye-based capillary filling experiments as well as electro-osmotic current-monitoring measurements. Using our model we predict the dependence of potential, surface charge density, and capillary filling length ratio on ionic strength for different surface compositions, which can be difficult to achieve otherwise. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:301 / 310
页数:10
相关论文
共 50 条
[1]  
[Anonymous], 2009, J AM CHEM SOC, DOI DOI 10.1021/JA906434C
[2]   SURFACE HYDROXYLATION OF SILICA [J].
ARMISTEAD, CG ;
TYLER, AJ ;
HAMBLETON, FH ;
MITCHELL, SA ;
HOCKEY, JA .
JOURNAL OF PHYSICAL CHEMISTRY, 1969, 73 (11) :3947-+
[3]   Towards an understanding of induced-charge electrokinetics at large applied voltages in concentrated solutions [J].
Bazant, Martin Z. ;
Kilic, Mustafa Sabri ;
Storey, Brian D. ;
Ajdari, Armand .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2009, 152 (1-2) :48-88
[4]   The charge of glass and silica surfaces [J].
Behrens, SH ;
Grier, DG .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (14) :6716-6721
[5]   Electrostatic free energy of interacting ionizable double layers [J].
Biesheuvel, PM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2004, 275 (02) :514-522
[6]   Application of the charge regulation model to the separation of ions by hydrophilic membranes [J].
Biesheuvel, PM ;
de Lint, WBS .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 241 (02) :422-427
[7]   Nanofluidics, from bulk to interfaces [J].
Bocquet, Lyderic ;
Charlaix, Elisabeth .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (03) :1073-1095
[8]   4-LAYER COMPLEXATION MODEL FOR ION ADSORPTION AT ELECTROLYTE/OXIDE INTERFACE - THEORETICAL FOUNDATIONS [J].
CHARMAS, R ;
PIASECKI, W ;
RUDZINSKI, W .
LANGMUIR, 1995, 11 (08) :3199-3210
[9]   SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .2. SURFACE PROPERTIES OF AMORPHOUS IRON OXYHYDROXIDE AND ADSORPTION OF METAL-IONS [J].
DAVIS, JA ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 67 (01) :90-107
[10]   SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .1. COMPUTATION OF ELECTRICAL DOUBLE-LAYER PROPERTIES IN SIMPLE ELECTROLYTES [J].
DAVIS, JA ;
JAMES, RO ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 63 (03) :480-499