Nanoparticle-Driven Assembly of Block Copolymers: A Simple Route to Ordered Hybrid Materials
Journal of the American Chemical Society2011Vol. 133(17), pp. 6513–6516
Citations Over TimeTop 10% of 2011 papers
Abstract
The addition of nanoparticles that selectively hydrogen bond with one of the segments of a block copolymer is shown to induce order in otherwise disordered systems. This enables the fabrication of well-ordered hybrid materials with spherical, cylindrical, or lamellar domains at particle loadings of more than 40%, as evidenced by TEM and SAXS. The approach described is simple and applicable to a wide range of nanoparticles and block copolymers, and it lays the groundwork for the design of cooperatively assembled functional devices.
Related Papers
- → Crystallization induced microstructure of crystalline/crystalline poly(vinylidenefluoride)/poly(3-hydroxybutyrate) blends probed by small angle X-ray scattering(2001)66 cited
- → How to calculate starch lamellar features with improved accuracy by small angle X-ray scattering(2019)21 cited
- → Synchrotron SAXS and WAXS Studies on Changes in Structural and Thermal Properties of Poly[(R)‐3‐hydroxybutyrate] Single Crystals during Heating(2005)25 cited
- → Small‐angle X‐ray scattering from polyethylene: Distorted lamellar structures(2003)18 cited
- → Macrostructure of Melt-Crystallized Vinylidene Fluoride /Trifluoroethylene Copolymers (37/63, 65/35, 73/27 mol%)(1995)4 cited