Templated Self-Assembly of Square Symmetry Arrays from an ABC Triblock Terpolymer

被引:119
作者
Chuang, Vivian P. [2 ]
Gwyther, Jessica [1 ]
Mickiewicz, Rafal A. [2 ]
Manners, Ian [1 ]
Ross, Caroline A. [2 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[2] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
基金
英国工程与自然科学研究理事会;
关键词
BLOCK-COPOLYMER LITHOGRAPHY; THIN-FILMS; MORPHOLOGIES; GRAPHOEPITAXY; HOMOPOLYMER; CYLINDERS;
D O I
10.1021/nl902646e
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Self-assembly provides the ability to create well-controlled nanostructures with electronic or chemical functionality and enables the synthesis of a wide range of useful devices. Diblock copolymers self-assemble into periodic arrays of microdomains with feature sizes of typically 10-50 nm, and have been used to make a wide range of devices such as silicon capacitors and transistors, photonic crystals, and patterned magnetic media(1-3). However, the cylindrical or spherical microdomains in diblock copolymers generally form close-packed structures with hexagonal symmetry, limiting their device applications. Here we demonstrate self-assembly of square-symmetry patterns from a triblock terpolymer in which one organometallic block imparts high etch selectivity and etch resistance. Long-range order is imposed on the microdomain arrays by self-assembly on topographical substrates, and the orientation of both square lattices and in-plane cylinders is controlled by the substrate chemistry. Pattern transfer is demonstrated by making an array of square-packed 30 nm tall, 20 nm diameter silica pillars. Templated self-assembly of triblock terpolymers can generate nanostructures with geometries that are unattainable from diblock copolymers, significantly enhancing the capabilities of block copolymer lithography.
引用
收藏
页码:4364 / 4369
页数:6
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