Grant: Discovery Grants Program - Individual
Memorial University of Newfoundland
$43,613.00
Control and tunability of self assembly in colloidal soft matter: novel structures, materials science, and kinetics.
FY 2010-11
Summary
How materials self-organize into ordered structures, and how they get stuck in disordered states are among the most profound problems in condensed matter and biophysics. Monodisperse colloids in suspension can be conceived of as ""big atoms"" to study these fundamental problems. Self-assembly in colloids closely mimics thermodynamic phase behavior in atomic fluids. Tunability of colloidal interactions allows one to ""tune"" the colloidal free energy: external fields can tune the energetic contributions to the free energy while size and shape polydispersity can be used to control the entropic contributions.
New forms of experimental control lead to novel phenomena. In this proposal, complementary experimental techniques will be combined with an unprecedented control over interparticle interactions (via novel electric field geometries) and polydispersity to create novel equilibrium microscale and nanoscale colloidal structures, with applications in materials science and biophysics. Electric fields will be used as thermodynamic variables to traverse colloidal phase transitions, providing insights into fundamental non-equilibrium problems in condensed matter, such as the kinetics of crystallization and the glass transition.
We are studying colloidal suspensions in novel electric field geometries as well as anisotropic liquid-crystalline media in order to achieve greater control over crystal formation and impurity defect suppression. This will allow us to obtain more detailed information about kinetics in rare, extremely quick or extremely slow processes (crystal nucleation, crystal growth and the glass transition). External fields also enable us to make new kinds of nano-patterned materials, with applications as magnetic films, photonic crystals or electrorheological fluids. Advances in this field will thus result in materials with improved functionality.
Program
Discovery Grants Program - Individual
Recipient
Location
Newfoundland and Labrador, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
312443-2008
Name nom
Yethiraj, Anand
Department département
Physics and Physical Oceanography
Organization id
89
Institution établissement
Memorial University of Newfoundland
Province en
Newfoundland and Labrador
Province fr
Terre-Neuve-et-Labrador
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2008
Award amount
43613
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
28
Committee name en
Condensed Matter Physics
Committee name fr
Phys. de la matière condensée
Area of application code
1208
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Materials sciences
Area of application fr
Sciences des matériaux
Research subject code
3311
Research subject group en
Condensed matterphysics
Research subject group fr
Physique de la matière condensée
Research subject en
Soft condensed matter
Research subject fr
Matière condensée molle
Partie
3
Nb partie
5
Application title
Control and tunability of self assembly in colloidal soft matter: novel structures, materials science, and kinetics.
Keyword
NSERC
Application summary
How materials self-organize into ordered structures, and how they get stuck in disordered states are among the most profound problems in condensed matter and biophysics. Monodisperse colloids in suspension can be conceived of as ""big atoms"" to study these fundamental problems. Self-assembly in colloids closely mimics thermodynamic phase behavior in atomic fluids. Tunability of colloidal interactions allows one to ""tune"" the colloidal free energy: external fields can tune the energetic contributions to the free energy while size and shape polydispersity can be used to control the entropic contributions.
New forms of experimental control lead to novel phenomena. In this proposal, complementary experimental techniques will be combined with an unprecedented control over interparticle interactions (via novel electric field geometries) and polydispersity to create novel equilibrium microscale and nanoscale colloidal structures, with applications in materials science and biophysics. Electric fields will be used as thermodynamic variables to traverse colloidal phase transitions, providing insights into fundamental non-equilibrium problems in condensed matter, such as the kinetics of crystallization and the glass transition.
We are studying colloidal suspensions in novel electric field geometries as well as anisotropic liquid-crystalline media in order to achieve greater control over crystal formation and impurity defect suppression. This will allow us to obtain more detailed information about kinetics in rare, extremely quick or extremely slow processes (crystal nucleation, crystal growth and the glass transition). External fields also enable us to make new kinds of nano-patterned materials, with applications as magnetic films, photonic crystals or electrorheological fluids. Advances in this field will thus result in materials with improved functionality.