Patchy Polymer Colloids with Tunable Anisotropy Dimensions

被引:88
作者
Kraft, Daniela J. [1 ]
Hilhorst, Jan [1 ]
Heinen, Maria A. P. [1 ]
Hoogenraad, Mathijs J. [1 ]
Luigjes, Bob [1 ]
Kegel, Willem K. [1 ]
机构
[1] Univ Utrecht, Vant Hoff Lab Phys & Colloid Chem, Debye Inst NanoMat Sci, NL-3508 TC Utrecht, Netherlands
关键词
SEEDED EMULSION POLYMERIZATION; JANUS PARTICLES; NANOPARTICLES; MONODISPERSE; NETWORKS; SHAPE;
D O I
10.1021/jp108760g
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 the synthesis of polymer colloids with continuously tunable anisotropy dimensions: patchiness, roughness, and branching. Our method makes use of controlled fusion of multiple protrusions on highly cross-linked polymer particles produced by seeded emulsion polymerization. Carefully changing the synthesis conditions, we can tune the number of protrusions, or branching, of the obtained particles from spheres with one to three patches to raspberry-like particles with multiple protrusions. In addition to that, roughness is generated on the seed particles by adsorption of secondary nucleated particles during synthesis. The size of the roughness relative to the smooth patches can be continuously tuned by the initiator, surfactant, and styrene concentrations. Seed colloids chemically different from the protrusions induce patches of different chemical nature. The underlying generality of the synthesis procedure allows for application to a variety of seed particle sizes and materials. We demonstrate the use of differently sized polyNIPAM (poly-N-isopropylacrylamide), as well as polystyrene and magnetite filled polyNIPAM seed particles, the latter giving rise to magnetically anisotropic colloids. The high yield together with the uniform, anisotropic shape make them interesting candidates for use as smart building blocks in self-assembling systems.
引用
收藏
页码:7175 / 7181
页数:7
相关论文
共 32 条
[1]   Experimental Investigation of Selective Colloidal Interactions Controlled by Shape, Surface Roughness, and Steric Layers [J].
Badaire, Stephane ;
Cottin-Bizonne, Cecile ;
Stroock, Abraham D. .
LANGMUIR, 2008, 24 (20) :11451-11463
[2]   Shape selectivity in the assembly of lithographically designed colloidal particles [J].
Badaire, Stephane ;
Cottin-Bizonne, Cecile ;
Woody, Joseph W. ;
Yang, Allen ;
Stroock, Abraham D. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (01) :40-41
[3]   Hierarchical organization of colloidal particles:: From colloidal crystallization to supraparticle chemistry [J].
Edwards, Erik W. ;
Wang, Dayang ;
Mohwald, Helmuth .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2007, 208 (05) :439-445
[4]   Dielectrophoretic Assembly of Metallodielectric Janus Particles in AC Electric Fields [J].
Gangwal, Sumit ;
Cayre, Olivier J. ;
Velev, Orlin D. .
LANGMUIR, 2008, 24 (23) :13312-13320
[5]   Superparamagnetic composite colloids with anisotropic structures [J].
Ge, Jianping ;
Hu, Yongxing ;
Zhang, Tierui ;
Yin, Yadong .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (29) :8974-+
[6]   Self-assembly: From nanoscale to microscale colloids [J].
Glotzer, SC ;
Solomon, MJ ;
Kotov, NA .
AICHE JOURNAL, 2004, 50 (12) :2978-2985
[7]   Anisotropy of building blocks and their assembly into complex structures [J].
Glotzer, Sharon C. ;
Solomon, Michael J. .
NATURE MATERIALS, 2007, 6 (08) :557-562
[8]   Clusters of amphiphilic colloidal spheres [J].
Hong, Liang ;
Cacciuto, Angelo ;
Luijten, Erik ;
Granick, Steve .
LANGMUIR, 2008, 24 (03) :621-625
[9]   Formation of anisotropic polymer colloids by disparate relaxation times [J].
Kegel, Willem K. ;
Breed, Dana ;
Elsesser, Mark ;
Pine, David J. .
LANGMUIR, 2006, 22 (17) :7135-7136
[10]   Uniform nonspherical colloidal particles with tunable shapes [J].
Kim, Jin-Woong ;
Larsen, Ryan J. ;
Weitz, David A. .
ADVANCED MATERIALS, 2007, 19 (15) :2005-+