2-D assembly of colloidal particles on a planar electrode

被引:94
作者
Prieve, Dennis C. [1 ]
Sides, Paul J. [1 ]
Wirth, Christopher L. [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
Electrokinetics; Electrochemistry; Photonic materials; 2-D aggregation; AMPHIFUNCTIONALLY ELECTRIFIED INTERFACES; IN-SITU OBSERVATION; ELECTROPHORETIC DEPOSITION; ELECTROHYDRODYNAMIC FLOW; DOUBLE-LAYERS; KHZ; FIELD; CRYSTALS; AGGREGATION; MOTION;
D O I
10.1016/j.cocis.2010.01.005
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
Electrical voltage externally applied between parallel-plate electrodes can cause colloidal particles located near one of the electrodes to aggregate: thus monodisperse particles can be driven to form hexagonally close-packed arrays which can be useful in the fabrication of photonic materials. The mechanism for lateral motion of particles on the electrode surface is electroosmotic flow driven by the action of the applied electric field acting either on the equilibrium charges in the diffuse layer of the particles (ECEO) or on charge induced by the electric field on the surface of the electrode (ICEO). For steady currents. ECEO dominates whereas ICEO dominates for high-frequency alternating current. For intermediate frequencies (10 Hz to 1 kHz) both mechanisms are active. This critical review attempts to integrate concepts from electrochemistry and colloid chemistry to understand this electrokinetic phenomenon. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:160 / 174
页数:15
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