Electric field-reversible three-dimensional colloidal crystals

被引:63
作者
Gong, TY
Wu, DT
Marr, DWM [1 ]
机构
[1] Colorado Sch Mines, Dept Chem, Golden, CO 80401 USA
[2] Colorado Sch Mines, Dept Chem Engn, Golden, CO 80401 USA
关键词
D O I
10.1021/la0340697
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed a general method of ordering colloidal particles into three-dimensional crystals rapidly and reversibly using electric fields. The novel mechanisms involved appear to rely on a combination of induced dipole interactions and hydrodynamic flows to create close-packed, mechanically stable crystals. Because the effective interactions can be moderated using the applied field, colloids in a wide variety of size ranges can be crystallized. We show here the ordering of particles of diameter 200-450 nm and illustrate how the nucleation of these crystals can be directed through the selective application of the electric field. Since the time scale for crystallization is minutes, significantly faster than in previous methods, the crystallization method present here is expected to allow development of practical devices for photonics and other applications.
引用
收藏
页码:5967 / 5970
页数:4
相关论文
共 24 条
[1]   CLASSICAL GROWTH OF HARD-SPHERE COLLOIDAL CRYSTALS [J].
ACKERSON, BJ ;
SCHATZEL, K .
PHYSICAL REVIEW E, 1995, 52 (06) :6448-6460
[2]   Mesoscopically periodic photonic-crystal materials for linear and nonlinear optics and chemical sensing [J].
Asher, SA ;
Holtz, J ;
Weissman, J ;
Pan, GS .
MRS BULLETIN, 1998, 23 (10) :44-50
[3]   Large-scale synthesis of a silicon photonic crystal with a complete three-dimensional bandgap near 1.5 micrometres [J].
Blanco, A ;
Chomski, E ;
Grabtchak, S ;
Ibisate, M ;
John, S ;
Leonard, SW ;
Lopez, C ;
Meseguer, F ;
Miguez, H ;
Mondia, JP ;
Ozin, GA ;
Toader, O ;
van Driel, HM .
NATURE, 2000, 405 (6785) :437-440
[4]   Controlled growth of hard-sphere colloidal crystals [J].
Cheng, ZD ;
Russell, WB ;
Chaikin, PM .
NATURE, 1999, 401 (6756) :893-895
[5]   Crystallization kinetics of hard spheres in microgravity in the coexistence regime: Interactions between growing crystallites [J].
Cheng, ZD ;
Chaikin, PM ;
Zhu, JX ;
Russel, WB ;
Meyer, WV .
PHYSICAL REVIEW LETTERS, 2002, 88 (01) :4
[6]   SINGLE COLLOIDAL CRYSTALS [J].
CLARK, NA ;
HURD, AJ ;
ACKERSON, BJ .
NATURE, 1979, 281 (5726) :57-60
[7]   Structure of electrorheological fluids [J].
Dassanayake, U ;
Fraden, S ;
van Blaaderen, A .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (08) :3851-3858
[8]   Real-space imaging of nucleation and growth in colloidal crystallization [J].
Gasser, U ;
Weeks, ER ;
Schofield, A ;
Pusey, PN ;
Weitz, DA .
SCIENCE, 2001, 292 (5515) :258-262
[9]   Electrically switchable colloidal ordering in confined geometries [J].
Gong, T ;
Marr, DWM .
LANGMUIR, 2001, 17 (08) :2301-2304
[10]   Two-dimensional electrohydrodynamically induced colloidal phases [J].
Gong, TY ;
Wu, DT ;
Marr, DWM .
LANGMUIR, 2002, 18 (26) :10064-10067