Controlling Materials Properties through Self-Assembly of Amphiphilic Polymers and Nanoparticles
소속 :
연사 : Prof. So-Jung Park (Department of Chemistry, University of Pennsylvania)
일시 : 2011-08-19 16:00 ~
장소 : 500동 목암홀
일 시 : 2011년 8월 19일, 4:00 PM
장 소 : 500동 목암홀
-Abstract-
  For the past few years, my group has made several important discoveries towards understanding how nanoparticles self-assemble with amphiphilic polymers. Based on these studies, we have developed new hybrid materials with interesting magnetic and optical properties (e.g., “superparamagnetic polymersomes”, “nanoparticle microcapsules”, “multicomponent spiky metal nanoshells”). Furthermore, we have incorporated functional polymers such as conjugated polymers and DNA into amphiphilic structures, and have shown that their properties can be drastically modified through self-assembly (e.g., tunable photoluminescent properties of conjugated polymers, and enhanced binding properties of DNA). In particular, our nanoparticle-encapsulating DNA block-copolymer assemblies possessed unprecedentedly high binding constants, demonstrating that self-assembly is a powerful tool not only for making elaborate nanoscale architectures but also for manipulating materials properties
장 소 : 500동 목암홀
-Abstract-
  For the past few years, my group has made several important discoveries towards understanding how nanoparticles self-assemble with amphiphilic polymers. Based on these studies, we have developed new hybrid materials with interesting magnetic and optical properties (e.g., “superparamagnetic polymersomes”, “nanoparticle microcapsules”, “multicomponent spiky metal nanoshells”). Furthermore, we have incorporated functional polymers such as conjugated polymers and DNA into amphiphilic structures, and have shown that their properties can be drastically modified through self-assembly (e.g., tunable photoluminescent properties of conjugated polymers, and enhanced binding properties of DNA). In particular, our nanoparticle-encapsulating DNA block-copolymer assemblies possessed unprecedentedly high binding constants, demonstrating that self-assembly is a powerful tool not only for making elaborate nanoscale architectures but also for manipulating materials properties