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      Ultralarge-area block copolymer lithography via soft graphoepitaxy

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      Journal of Materials Chemistry
      Royal Society of Chemistry (RSC)

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          Epitaxial self-assembly of block copolymers on lithographically defined nanopatterned substrates.

          Parallel processes for patterning densely packed nanometre-scale structures are critical for many diverse areas of nanotechnology. Thin films of diblock copolymers can self-assemble into ordered periodic structures at the molecular scale (approximately 5 to 50 nm), and have been used as templates to fabricate quantum dots, nanowires, magnetic storage media, nanopores and silicon capacitors. Unfortunately, perfect periodic domain ordering can only be achieved over micrometre-scale areas at best and defects exist at the edges of grain boundaries. These limitations preclude the use of block-copolymer lithography for many advanced applications. Graphoepitaxy, in-plane electric fields, temperature gradients, and directional solidification have also been demonstrated to induce orientation or long-range order with varying degrees of success. Here we demonstrate the integration of thin films of block copolymer with advanced lithographic techniques to induce epitaxial self-assembly of domains. The resulting patterns are defect-free, are oriented and registered with the underlying substrate and can be created over arbitrarily large areas. These structures are determined by the size and quality of the lithographically defined surface pattern rather than by the inherent limitations of the self-assembly process. Our results illustrate how hybrid strategies to nanofabrication allow for molecular level control in existing manufacturing processes.
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            Block Copolymer Lithography: Periodic Arrays of 1011 Holes in 1 Square Centimeter

            M. Park (1997)
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              Density multiplication and improved lithography by directed block copolymer assembly.

              Self-assembling materials spontaneously form structures at length scales of interest in nanotechnology. In the particular case of block copolymers, the thermodynamic driving forces for self-assembly are small, and low-energy defects can get easily trapped. We directed the assembly of defect-free arrays of isolated block copolymer domains at densities up to 1 terabit per square inch on chemically patterned surfaces. In comparing the assembled structures to the chemical pattern, the density is increased by a factor of four, the size is reduced by a factor of two, and the dimensional uniformity is vastly improved.
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                Author and article information

                Journal
                JMACEP
                Journal of Materials Chemistry
                J. Mater. Chem.
                Royal Society of Chemistry (RSC)
                0959-9428
                1364-5501
                2011
                2011
                : 21
                : 16
                : 5856
                Article
                10.1039/c0jm04248j
                2fa747ad-f909-4cc5-baf6-9d1adc1ae5ca
                © 2011
                History

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