Sunday, October 26, 2008

NC State engineers discover nanoparticles can break on through

Jan Genzer

Jan Genzer, Ph. D., Materials Science and Engineering, University of Pennsylvania (1996).

Areas of Interest: Behavior of polymers at surfaces and interfaces, Polymer thermodynamics, Materials self-assembly.

Email: Research Group:, Phone: 919-515-2069
In a finding that could speed the use of sensors or barcodes at the nanoscale, North Carolina State University engineers have shown that certain types of tiny organic particles, when heated to the proper temperature, bob to the surface of a layer of a thin polymer film and then can reversibly recede below the surface when heated a second time.

Selectively bringing a number of particles to a surface and then sinking them back below it results in controllable surface patterns. According to NC State researchers involved in the project, patterning surfaces is one of the holy grails of current nanotechnology research, and is difficult to do with certain particles. They add that the finding could result in tiny reusable bar codes, or in small fluorescent features that turn off when they sense too much heat or the presence of a certain chemical.
Dr. Jan Genzer, professor of chemical and biomolecular engineering, and Dr. Richard Spontak, professor of chemical and biomolecular engineering and materials science and engineering, published their finding along with graduate students Arif Gozen and Bin Wei in the journal Nano Letters.
They worked with engineers who designed the unique particles at the University of Melbourne in Australia.
The researchers used a special type of organic nanoparticle called a core-shell microgel in which the core of a cross-linked, or networked, polymer is surrounded by a shell of a different polymer.
Richard J. Spontak

Richard J. Spontak, Professor, Ph.D., Chemical Engineering, University of California at Berkeley 1988, B.S., Chemical Engineering, Pennsylvania State University 1983.

Areas of interest: Polymer morphology and phase stability, Multifunctional and nanostructured polymers, blends and networks. Application of microscopy techniques to polymer science and engineering.

Email:, Phone: 919.515.4200
"Most polymers are chain-like macromolecules that are like very long, cooked spaghetti noodles, but these special core-shell particles are shaped more like squash balls of one polymer with a fuzzy surface of a different polymer," Spontak says.

Heating these approximately 30-nanometer particles - which are hundreds of times smaller than a human hair - allows them to break through a polymer/polymer interface like a submarine coming to the surface of water. Reheating the particles at a polymer surface sinks them back below the surface. "This technique allows us to place the particles right where we want them - on the surface of a thin film," Genzer says. "It can be used to create a reusable bar code, for instance, or other functional polymer surfaces." ###
Note to editors: The abstract of the paper follows.

"Autophobicity-Driven Surface Segregation and Patterning of Core-Shell Microgel Nanoparticles"

Authors: Bin Wei, Arif O. Gozen, Richard J. Spontak and Jan Genzer, North Carolina State University; Paul A. Gurr, Anton Blencowe, David H. Solomon and Greg G. Qiao, University of Melbourne. Published: Online Aug. 8, 2008, in Nano Letters

Abstract: Core-shell microgel (CSMG) nanoparticles, also referred to as core-cross-linked star (CCS) polymers, can be envisaged as permanently cross-linked block copolymer micelles and, as such, afford novel opportunities for chemical functionalization, templating, and encapsulation. In this study, we explore the behavior of CSMG nanoparticles comprising a poly(methyl methacrylate) (PMMA) shell in molten PMMA thin films. Because of the autophobicity between the densely packed, short PMMA arms of the CSMG shell and the long PMMA chains in the matrix, the nanoparticles migrate to the film surface.

They cannot, however, break through the surface because of the inherently high surface energy of PMMA. Similar thermal treatment of CSMG-containing PMMA thin films with a polystyrene (PS) capping layer replaces surface energy at the PMMA/air interface by interfacial energy at the PMMA/PS interface, which reduces the energy barrier by an order of magnitude, thereby permitting the nanoparticles to emerge out of the PMMA bulk. This nanoscale process is reversible and can be captured at intermediate degrees of completion. Moreover, it is fundamentally general and can be exploited as an alternative means by which to reversibly pattern or functionalize polymer surfaces for applications requiring responsive nanolithography.

Contact: Mick Kulikowski 919-515-8387 North Carolina State University

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