Atomically Flat, 2D Edge-Directed Self-Assembly of Block Copolymers

被引:4
|
作者
Kim, Jang Hwan [1 ,2 ]
Jeong, Hyeon U. [3 ]
Yeom, Hye-In [4 ]
Han, Kyu Hyo [1 ,2 ]
Yang, Geon Gug [1 ,2 ]
Choi, Hee Jae [1 ,2 ]
Kim, Jong Min [4 ]
Park, Sang-Hee Ko [4 ]
Jin, Hyeong Min [5 ]
Kim, Jaeup U. U. [3 ]
Kim, Sang Ouk [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Natl Creat Res Initiat CRI, Ctr Multidimens Directed Nanoscale Assembly, Dept Mat Sci & Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol KAIST, KAIST Inst NanoCentury, Daejeon 34141, South Korea
[3] UNIST, Dept Phys, Ulsan 44919, South Korea
[4] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Daejeon 34141, South Korea
[5] Chungnam Natl Univ, Dept Organ Mat Engn, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
2D materials; block copolymers; directed self-assembly; graphene nanoribbons; BORON-NITRIDE NANOSHEETS; RAMAN-SPECTROSCOPY; SURFACE-ENERGY; SINGLE-LAYER; GRAPHENE; TRANSISTORS; TRANSPORT;
D O I
10.1002/adma.202207338
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoscale shape engineering is an essential requirement for the practical use of 2D materials, aiming at precisely customizing optimal structures and properties. In this work, sub-10-nm-scale block copolymer (BCP) self-assembled nanopatterns finely aligned along the atomic edge of 2D flakes, including graphene, MoS2, and h-BN, are exploited for reliable nanopatterning of 2D materials. The underlying mechanism for the alignment of the self-assembled nanodomains is elucidated based on the wetting layer alternation of the BCP film in the presence of intermediate 2D flakes. The resultant highly aligned nanocylinder templates with remarkably low levels of line edge roughness (LER) and line-width roughness (LWR) yield a sub-10-nm-wide graphene nanoribbon (GNR) array with noticeable switching characteristics (on-to-off ratio up to approximate to 6 x 10(4)).
引用
收藏
页数:8
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