The new method is much faster, and reduces the number of steps in the process to just two: lithography and plasma etching.
Manufacturers constantly struggle to pack more transistors in less space, yet as the size of those transistors approaches the atomic scale, there are physical limits on how small they are able to make the patterns for the circuitry.
To achieve the incredibly tiny size required for the circuitry in future semiconductor electronics, computer chip makers are developing directed self-assembly, a large-scale, nano-patterning technique that can increase the density of circuit patterns and circumvent some limitations of conventional lithographic processes for printing circuits on wafers of semiconductors such as silicon. This enables the fabrication of intricate, perfectly ordered polymer patterns for circuitry.
Now, taking advantage of a germanium wafer coated with a layer of virtually pristine graphene—a sheet of carbon arranged just one atom thick—a team of engineers from the University of Wisconsin-Madison and the University of Chicago has devised a simpler, reproducible and less expensive manufacturing approach using directed self-assembly.
Electrical engineer Zhenqiang “Jack” Ma and materials engineer Michael Arnold of UW–Madison, chemical engineer Paul Nealey of the University of Chicago, and their students published details of the advance in the journal Scientific Reports.
For directed self-assembly, the researchers use conventional chemical techniques to define a pre-pattern. When chains of molecules known as block copolymers self-assemble on the pre-pattern, they follow the pattern to form well-ordered features. This new method is much faster, and reduces the number of steps in the process to just two: lithography and plasma etching.
In the first demonstration of their technique, the researchers used electron beam lithography and a mild plasma etching technique to pattern one-atom-thick graphene stripes on a germanium wafer. Then they spin-coated the wafer with a common block copolymer called polystyrene-block-poly(methyl methacrylate).
When heated, the block copolymer self-assembled completely in just 10 minutes—compared to 30 minutes using conventional chemical patterns—and with fewer defects. The researchers attribute this rapid assembly to the smooth, rigid, crystalline surfaces of germanium and graphene.
__Figure 1:__ *Chemical patterns consisting of alternating graphene and germanium stripes (left side) are used to direct the self-assembly of block copolymers into well-ordered patterns (right side). The top images are schematics and the bottom images are scanning electron micrographs. The scale bars are 200nm.*
Their new method takes advantage of a phenomenon called density multiplication. The researchers used electron beam lithography to first create a larger master template with sparse patterns that guide the orientation of their block copolymers.
When they directed the block copolymer to self-assemble, it did so in a way that enhanced the resolution of the original template—in this case, by a factor of 10. The best previous enhancement by density multiplication was a factor of four.
While the stripe pattern was a simple demonstration of their technique, the researchers also showed it works with more architecturally complex or irregular patterns, including those with abrupt 90-degree bends.
“These templates offer an exciting alternative to traditional chemical patterns composed of polymer mats and brushes, as they provide faster assembly kinetics and broaden the processing window, while also offering an inert, mechanically and chemically robust, and uniform template with well-defined and sharp material interfaces,” said Nealey.
The technique enables them to combine the uniformity and simpler processing of traditional “top-down” lithographic methods with the advantages of “bottom-up” assembly and greater density multiplication, and offers a promising route for large-scale production at significantly reduced cost.
“Using this one-atom-thick graphene template has never been done before. It’s a new template to guide the self-assembly of the polymers,” said Ma. “This is mass-production-compatible. We opened the door to even smaller features.”