We study the cylinder to sphere morphological transition of diblock copolymers in aqueous solution with a hydrophobic block and a charged block. We find a metastable undulated cylinder configuration for a range of charge and salt concentrations which, nevertheless, occurs above the threshold where spheres are thermodynamically favorable. By modeling the shape of the cylinder ends, we find that the free-energy barrier for the transition from cylinders to spheres is quite large and that this barrier falls significantly in the limit of high polymer charge and low solution salinity. This suggests that observed undulated cylinder phases are kinetically trapped structures
The morphological transition from vesicles to inverted hexagonally packed (hollow) rods was studied ...
ABSTRACT: We have developed a scaling theory for a salt-free solution of diblock polyampholytes. A c...
We report on the structures exhibited by two different diblock poly(styrene)-b-poly(acrylic acid) (P...
We study the cylinder to sphere morphological transition of diblock copolymers in aqueous solution w...
Using scaling arguments, we consider dilute solutions of diblock-copolymers consisting of a strongl...
We investigate the structural behavior of a poly(styrene)-block-poly(acrylic acid) diblock copolymer...
We present a mean-field theory to describe micelles formed by diblock copolymer with one neutral and...
The structure of diblock copolymers micelles depends on a delicate balance of thermodynamic forces d...
Direct visualization of Morphological evolution remains extremely challenging despite its critical i...
Aggregate morphologies as a function of apparent pH (PH*) have been studied for PS-b-P4VP diblocks i...
Assemblies of block copolymer amphiphiles are sometimes viewed as glassy, frozen, or static colloids...
Direct visualization of morphological evolution remains extremely challenging despite its critical i...
The influence of confinement on morphology formation in copolymer systems is an important area of in...
(Communicated by the associate editor name) Abstract. We study the evolution of diblock copolymer me...
The phase behavior of a symmetric styrene−isoprene (SI) diblock copolymer in a styrene-selective sol...
The morphological transition from vesicles to inverted hexagonally packed (hollow) rods was studied ...
ABSTRACT: We have developed a scaling theory for a salt-free solution of diblock polyampholytes. A c...
We report on the structures exhibited by two different diblock poly(styrene)-b-poly(acrylic acid) (P...
We study the cylinder to sphere morphological transition of diblock copolymers in aqueous solution w...
Using scaling arguments, we consider dilute solutions of diblock-copolymers consisting of a strongl...
We investigate the structural behavior of a poly(styrene)-block-poly(acrylic acid) diblock copolymer...
We present a mean-field theory to describe micelles formed by diblock copolymer with one neutral and...
The structure of diblock copolymers micelles depends on a delicate balance of thermodynamic forces d...
Direct visualization of Morphological evolution remains extremely challenging despite its critical i...
Aggregate morphologies as a function of apparent pH (PH*) have been studied for PS-b-P4VP diblocks i...
Assemblies of block copolymer amphiphiles are sometimes viewed as glassy, frozen, or static colloids...
Direct visualization of morphological evolution remains extremely challenging despite its critical i...
The influence of confinement on morphology formation in copolymer systems is an important area of in...
(Communicated by the associate editor name) Abstract. We study the evolution of diblock copolymer me...
The phase behavior of a symmetric styrene−isoprene (SI) diblock copolymer in a styrene-selective sol...
The morphological transition from vesicles to inverted hexagonally packed (hollow) rods was studied ...
ABSTRACT: We have developed a scaling theory for a salt-free solution of diblock polyampholytes. A c...
We report on the structures exhibited by two different diblock poly(styrene)-b-poly(acrylic acid) (P...