The article (see below) appeared on the website (http://www.nsls.bnl.gov/newsroom/science/2010/07-419.asp) on 15 July 2010 with the headline: "Lessening the Penalty for Creating Block Copolymer Nanostructures": How do you make a material that has the elasticity of a rubber band and the thermal insulation of a Styrofoam cup? Connect two distinct polymer chains - poly(isoprene) and poly(styrene) - end to end like a series of children's building blocks. The result is an appropriately named "block copolymer" that boasts the properties of both materials and is commonly used in the tires of automobiles and the soles of athletic shoes. But the most impressive trait of a block copolymer is its ability to self-assemble. Imagine, for example, dropping a mixture of poly(isoprene) and poly(styrene) on the floor. The two incompatible blocks will "phase separate" like oil and water. However, connect the ends of the two polymers together and the material usually can assemble into a well-defined material with nanoscale structure. The natural assembly is extremely valuable for emerging nanoscale applications, including materials for fuel cells, lithium ion batteries, and organic photovoltaics. "Block copolymers can create well-defined nanostructures without traditional nanoscale processing," said University of Delaware researcher Thomas Epps. "The usage of block copolymers can help augment or replace lithographic and other techniques, meaning one can make nanoscale materials without the expensive tools." In order to take full advantage of a block copolymer's molecular architecture, researchers are looking for ways to control the interactions between polymer blocks through means such as high temperatures and selective solvents. "When I make a copolymer of a certain composition and molecular weight, I have typically locked myself into a processing temperature based on those chemical factors," Epps said. "We want to find a way to tune these materials so that, no matter what blocks are being combined, we can control the processing conditions." To do this, Epps and fellow University of Delaware researchers Nripen Singh and Maeva Tureau are exploring tuning with tapering, which increases the compatibility of the polymer by smoothing out the chemical interface between the two blocks. Tapering conceptualized: think of a block of purple beads linked to a block of blue beads. A regular block copolymer will have a sharp interface separating the two types of beads. In a tapered block copolymer, a region between the two blocks has been inserted such that the number of purple beads will slowly decrease as the number of blue beads increases. In an inverse tapered block copolymer, the opposite occurs (see figure). Tapering the interface is thought to reduce the "penalty" of mixing between the two very different blocks. The result is a lower processing temperature, which is easier and cheaper to achieve, and greater chemical compatibility. To test this idea, the researchers synthesized a number of tapered poly(isoprene-b-styrene) block copolymer samples at the University of Delaware: samples with different taper lengths (from 15-35 percent tapered material) with either normal or inverse tapering. The samples were then heated and cooled while researchers observed the changes in the material with small-angle x-ray scattering at the NSLS (beamline X27C) and Argonne's Advanced Photon Source, and transmission electron microscopy and dynamic mechanical analysis at the University of Delaware. Their results, which appeared in the December 7, 2009 issue of Soft Matter, proved that researchers can tune the compatibility of block copolymers (via tapering) with no detriment to the ordering or mechanical properties of the material. The research also revealed that inverse tapering gives the greatest increase in compatibility. "The inverse tapering forces more unfavorable interactions in the as-synthesized copolymer so the penalty for creating more interactions through self-assembly or mixing is smaller," Epps said. Funding for this study was provided by the National Science Foundation and the Department of Commerce. The NSLS is supported by the U.S. Department of Energy Office of Science." [PUBLICATION: N. Singh, M.S. Tureau, T.H. Epps, III, "Manipulating Ordering Transitions in Interfacially Modified Block Copolymers,"Soft Matter, 5, 4757-4762 (2009)] (The copolyolefins with tapered block structure are subject of USP 7,758,832.)
The National Synchrotron Light Source at Brookhaven National Laboratory in New York, is a national user research facility funded by the U.S. Department of Energy's Office of Basic Energy Science. The NSLS operates two electron storage rings: an X-Ray ring and a Vacuum UltraViolet (VUV) ring which provide intense light spanning the electromagnetic spectrum from the infrared through x-rays.