Multicompartment and multigeometry nanoparticle assembly
Author(s) -
Darrin J. Pochan,
Jiahua Zhu,
Ke Zhang,
Karen L. Wooley,
Caroline Miesch,
Todd Emrick
Publication year - 2011
Publication title -
soft matter
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 170
eISSN - 1744-6848
pISSN - 1744-683X
DOI - 10.1039/c0sm00960a
Subject(s) - nanoparticle , copolymer , particle (ecology) , nanoscopic scale , materials science , block (permutation group theory) , nanotechnology , phase (matter) , kinetic energy , chemical physics , self assembly , nanostructure , molecular dynamics , chemistry , polymer , physics , computational chemistry , composite material , geometry , oceanography , mathematics , organic chemistry , quantum mechanics , geology
The directed or dynamic assembly of molecular components in solution is a simple and effective strategy to confine materials in desired geometries and length scales. We use a kinetic control strategy with block copolymer blending to construct complex nanoparticles through the demixing of unlike block copolymers within the same nanoscale particle. Successful nanoparticle construction relies on kinetic trapping of unlike block copolymers into the same nanoparticle with solution processing. Not only can we make nanoparticles with multiple internal compartments of a desired size, but we can also make nanoparticles of hybrid geometries (e.g. a blend of cylindrical and spherical geometries). These combination particles are kinetically trapped, non-equilibrium structures. However, the block copolymers are able to phase separate locally within the nanoscale particle, thus producing internal compartments and hybrid geometries.
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