Grant: Discovery Grants Program - Individual
St. Francis Xavier University
$18,780.00
Theoretical study of block copolymer self-assembly
EF 2007-08
Résumé
Polymers are long, chain-like molecules that can occur naturally (e.g., DNA) or can be produced in the lab via synthetic techniques (e.g., polystyrene). The rubber and plastics in our everyday lives are made of polymers. Block copolymers are produced by specialized synthetic techniques that chemically bond the end of one polymer species, or block (e.g., polystyrene) to a different polymer species (e.g., polyisoprene). The tendency for unlike blocks to repel would lead the system to separate into macroscopic domains of each species, if it weren't for the chemical bond between the blocks. The best the block copolymer can do is to separate its blocks into domain structures on a scale set by the size of the polymer, that is, tens of nanometers. The ability to spontaneously organize (self-assemble) into these microstructures make these materials potentially useful in applications requiring such resolution. For example, there is an ongoing, world-wide effort to investigate the use of block copolymers as structural templates for lithography, and for the production of ordered arrays of metallic nano-dots and nano-wires. These templates hold the promise of shrinking microelectronic circuits to the 10 nm scale, below that accessible to traditional photolithography. One aspect of my research centres on understanding how confinement of a block copolymer into a cylindrical nanopore influences the self-assembly process and creates new microstructures. This may lead to potentially novel applications. When processing these materials it is also important to have a fundamental understanding of the time it takes the system to form these structures, that is, the kinetics of self-assembly. This is another research focus of my group. Key questions are: What is the relation between microstructure and dynamics? What are the kinetic pathways for, and barriers to, the formation of a given structure? How do we formulate a non-equilibrium theory to answer these questions? My group tackles these problems using a combination of sophisticated analytical methods and high-performance computing. This work is expected to result in major advances in our understanding of the dynamics of block copolymers, and will enhance Canada's overall research effort in novel, soft-materials.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Nova Scotia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
288213-2007
Name nom
Wickham, Robert
Department département
Physics
Organization id
83
Institution établissement
St. Francis Xavier University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2007
Award amount
18780
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
508
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Polymers, rubber and plastics
Area of application fr
Polymères, caoutchouc et plastiques
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
1
Nb partie
5
Application title
Theoretical study of block copolymer self-assembly
Keyword
NA
Application summary
Polymers are long, chain-like molecules that can occur naturally (e.g., DNA) or can be produced in the lab via synthetic techniques (e.g., polystyrene). The rubber and plastics in our everyday lives are made of polymers. Block copolymers are produced by specialized synthetic techniques that chemically bond the end of one polymer species, or block (e.g., polystyrene) to a different polymer species (e.g., polyisoprene). The tendency for unlike blocks to repel would lead the system to separate into macroscopic domains of each species, if it weren't for the chemical bond between the blocks. The best the block copolymer can do is to separate its blocks into domain structures on a scale set by the size of the polymer, that is, tens of nanometers. The ability to spontaneously organize (self-assemble) into these microstructures make these materials potentially useful in applications requiring such resolution. For example, there is an ongoing, world-wide effort to investigate the use of block copolymers as structural templates for lithography, and for the production of ordered arrays of metallic nano-dots and nano-wires. These templates hold the promise of shrinking microelectronic circuits to the 10 nm scale, below that accessible to traditional photolithography. One aspect of my research centres on understanding how confinement of a block copolymer into a cylindrical nanopore influences the self-assembly process and creates new microstructures. This may lead to potentially novel applications. When processing these materials it is also important to have a fundamental understanding of the time it takes the system to form these structures, that is, the kinetics of self-assembly. This is another research focus of my group. Key questions are: What is the relation between microstructure and dynamics? What are the kinetic pathways for, and barriers to, the formation of a given structure? How do we formulate a non-equilibrium theory to answer these questions? My group tackles these problems using a combination of sophisticated analytical methods and high-performance computing. This work is expected to result in major advances in our understanding of the dynamics of block copolymers, and will enhance Canada's overall research effort in novel, soft-materials.