Formation of ordered nanocluster arrays by self-assembly on nanopatterned Si(100) surfaces

被引:21
作者
Winningham, TA
Gillis, HP [1 ]
Choutov, DA
Martin, KP
Moore, JT
Douglas, K
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Colorado, Dept Phys, Boulder, CO 80309 USA
[3] Georgia Inst Technol, Ctr Microelect Res, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
adatoms; atomic force microscopy; clusters; etching; nucleation; self-assembly; silicon; surface diffusion;
D O I
10.1016/S0039-6028(98)00115-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A precisely ordered and precisely located array of 5 nm diameter nanoclusters has been fabricated by first etching into the substrate an array of holes with diameters comparable with the size of nanoclusters sought and then depositing adatoms on the substrate. The severely restricted diffusion field defined by the holes dominates nucleation and growth to produce a single nanocluster in each etched hole. Using low energy electron enhanced etching in a DC hydrogen plasma, we transferred an hexagonal array of 18 nm diameter holes with a 22 nm lattice constant from a biologically derived mask into Si(100). After etching, the mask was removed, and the patterned surface was intentionally oxidized in an oxygen plasma. Deposition of 1.2 nm of Ti on the oxidized surface produced an ordered array of 5 nm diameter metal nanoclusters positioned at the etched hole sites. Our methods achieved massively parallel processing at the key fabrication steps of pattern generation, pattern transfer, and nanocluster formation. Therefore, our methods enable rapid fabrication of arrays for fundamental studies and provide a route to manufacturability of nanostructure arrays for technological purposes. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:221 / 228
页数:8
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