Three-Tone Chemical Patterns for Block Copolymer Directed Self-Assembly.

Chemical patterns for directed self-assembly (DSA) of lamellae-forming block copolymers (BCP) with density multiplication can be fabricated by patterning resist on a cross-linked polystyrene layer, etching to create guide stripes, and depositing end-grafted brushes in between the stripes as background. To date, two-tone chemical patterns have been targeted with the guide stripes preferentially wet by one block of the copolymer and the background chemistry weakly preferentially wet by the other block. In the course of fabricating chemical patterns in an all-track process using 300 mm wafers, it was discovered that the etching process followed by brush grafting could produce a three-tone pattern. We characterized the three regions of the chemical patterns with a combination of SEM, grazing-incidence small-angle X-ray scattering (GISAXS), and assessment of BCP-wetting behavior, and evaluated the DSA behavior on patterns over a range of guide stripe widths. In its best form, the three-tone pattern consists of guide stripes preferentially wet by one block of the copolymer, each flanked by two additional stripes that wet the other block of the copolymer, with a third chemistry as the background. Three-tone patterns guide three times as many BCP domains as two-tone patterns and thus have the potential to provide a larger driving force for the system to assemble into the desired architecture with fewer defects in shorter time and over a larger process window.

[1]  Johner,et al.  Can a polymer brush trap a wetting layer? , 1992, Physical review letters.

[2]  F. Bates,et al.  Polyisoprene-Polystyrene Diblock Copolymer Phase Diagram near the Order-Disorder Transition , 1995 .

[3]  Craig J. Hawker,et al.  Interfacial Segregation in Disordered Block Copolymers: Effect of Tunable Surface Potentials , 1997 .

[4]  G. Fredrickson,et al.  Block Copolymers—Designer Soft Materials , 1999 .

[5]  A. Mayes,et al.  Block copolymer thin films : Physics and applications , 2001 .

[6]  P. Nealey,et al.  Epitaxial self-assembly of block copolymers on lithographically defined nanopatterned substrates , 2003, Nature.

[7]  E. W. Edwards,et al.  Precise Control over Molecular Dimensions of Block‐Copolymer Domains Using the Interfacial Energy of Chemically Nanopatterned Substrates , 2004 .

[8]  Juan J. de Pablo,et al.  Dimensions and Shapes of Block Copolymer Domains Assembled on Lithographically Defined Chemically Patterned Substrates , 2007 .

[9]  R. Ruiz,et al.  Density Multiplication and Improved Lithography by Directed Block Copolymer Assembly , 2008, Science.

[10]  E. Han,et al.  Effect of Composition of Substrate-Modifying Random Copolymers on the Orientation of Symmetric and Asymmetric Diblock Copolymer Domains , 2008 .

[11]  Mark Wylie,et al.  Critical dimension uniformity using reticle inspection tool , 2009, Photomask Technology.

[12]  김지은,et al.  Spontaneous Lamellar Alignment in Thickness-Modulated Block Copolymer Films , 2009 .

[13]  Hyo Seon Suh,et al.  Thickness Dependence of Neutral Parameter Windows for Perpendicularly Oriented Block Copolymer Thin Films , 2010 .

[14]  Juan J. de Pablo,et al.  Interpolation in the Directed Assembly of Block Copolymers on Nanopatterned Substrates: Simulation and Experiments , 2010 .

[15]  Joy Y. Cheng,et al.  Simple and versatile methods to integrate directed self-assembly with optical lithography using a polarity-switched photoresist. , 2010, ACS nano.

[16]  Juan J. de Pablo,et al.  Mechanism and dynamics of block copolymer directed assembly with density multiplication on chemically patterned surfaces , 2010 .

[17]  Eungnak Han,et al.  Fabrication of Lithographically Defined Chemically Patterned Polymer Brushes and Mats , 2011 .

[18]  Jo Finders,et al.  Toward 22 nm: fast and effective intrafield monitoring and optimization of process windows and critical dimension uniformity , 2011 .

[19]  Mark Neisser,et al.  Implementation of a chemo-epitaxy flow for directed self-assembly on 300-mm wafer processing equipment , 2012 .

[20]  X. Gu,et al.  Unidirectionally aligned line patterns driven by entropic effects on faceted surfaces , 2012, Proceedings of the National Academy of Sciences.

[21]  Juan J. de Pablo,et al.  Chemical Patterns for Directed Self-Assembly of Lamellae-Forming Block Copolymers with Density Multiplication of Features , 2013 .

[22]  Marcus Müller,et al.  Computational Approaches for the Dynamics of Structure Formation in Self-Assembling Polymeric Materials , 2013 .

[23]  Frank S Bates,et al.  Directed assembly of lamellae forming block copolymer thin films near the order-disorder transition. , 2014, Nano letters.

[24]  Lei Wan,et al.  Evolutionary Optimization of Directed Self-Assembly of Triblock Copolymers on Chemically Patterned Substrates. , 2014, ACS macro letters.

[25]  M. Perego,et al.  Ordering dynamics in symmetric PS-b-PMMA diblock copolymer thin films during rapid thermal processing , 2014 .

[26]  Yi Cao,et al.  Tuning the strength of chemical patterns for directed self-assembly of block copolymers , 2014, Advanced Lithography.

[27]  Marcus Müller,et al.  Defect removal in the course of directed self-assembly is facilitated in the vicinity of the order-disorder transition. , 2014, Physical review letters.

[28]  Roel Gronheid,et al.  Grazing-incidence small angle x-ray scattering studies of nanoscale polymer gratings , 2015, Advanced Lithography.

[29]  Lei Wan,et al.  Double-Patterned Sidewall Directed Self-Assembly and Pattern Transfer of Sub-10 nm PTMSS-b-PMOST. , 2015, ACS applied materials & interfaces.

[30]  Jianhui Shan,et al.  Toward high-performance quality meeting IC device manufacturing requirements with AZ SMART DSA process , 2015, Advanced Lithography.