Selective chain reaction of acetone leading to the successive growth of mutually perpendicular molecular lines on the Si(100)-(2x1)-H surface

被引:30
作者
Hossain, Md. Zakir [1 ]
Kato, Hiroyuki S.
Kawai, Maki
机构
[1] RIKEN, Inst Phys & Chem Res, Wako, Saitama 35101, Japan
[2] Univ Tokyo, Dept Adv Mat, Chiba 277, Japan
关键词
D O I
10.1021/ja074464+
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The successive growth of mutually perpendicular molecular lines from one dangling-bond (DB) site on the Si(100)-(2x1)-H surface has been realized through a substrate-mediated chain reaction at 300 K. Among various molecules, acetone molecules undergo the most facile chain reaction with a DB site, which proceeds selectively on the Si(100)-(2x1)-H surface, resulting in only single molecular lines in the parallel-row (parallel to the dimer row) direction. The smaller size and higher reactivity of acetone molecules enable us to successively grow a parallel-row acetone line from the end of a cross-row (perpendicular to the dimer row) allylmercaptan line simply by changing the feed of gas molecules into the reaction chamber. Since the length of a molecular line is controlled by the number of gas molecules impinged, it is possible to turn a chain reaction from the cross-row direction to the parallel-row direction at any desired point on the surface. The reaction path of the adsorbing molecules is discussed. The present study provides a new means of fabricating mutually perpendicular molecular lines through a chain reaction initiating at a preselected DB site on the Si(100)-(2x1) surface.
引用
收藏
页码:12304 / 12309
页数:6
相关论文
共 23 条
[1]   Room temperature nanofabrication of atomically registered heteromolecular organosilicon nanostructures using multistep feedback controlled lithography [J].
Basu, R ;
Guisinger, NP ;
Greene, ME ;
Hersam, MC .
APPLIED PHYSICS LETTERS, 2004, 85 (13) :2619-2621
[2]   Organic functionalization of group IV semiconductor surfaces: principles, examples, applications, and prospects [J].
Bent, SF .
SURFACE SCIENCE, 2002, 500 (1-3) :879-903
[3]   SCANNING TUNNELING MICROSCOPY STUDY OF THE ADSORPTION AND RECOMBINATIVE DESORPTION OF HYDROGEN FROM THE SI(100)-2X1 SURFACE [J].
BOLAND, JJ .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1992, 10 (04) :2458-2464
[4]   Dispersion interactions enable the self-directed growth of linear alkane nanostructures covalently bound to silicon [J].
DiLabio, GA ;
Piva, PG ;
Kruse, P ;
Wolkow, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (49) :16048-16050
[5]   Probing charge transport at the single-molecule level on silicon by using cryogenic ultra-high vacuum scanning tunneling microscopy [J].
Guisinger, NP ;
Yoder, NL ;
Hersam, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (25) :8838-8843
[6]   Flexible electronic futures [J].
Hamers, RJ .
NATURE, 2001, 412 (6846) :489-490
[7]   Competing forward and reversed chain reactions in one-dimensional molecular line growth on the Si(100)-(2 x 1)-H surface [J].
Hossain, Md. Zakir ;
Kato, Hiroyuki S. ;
Kawai, Maki .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (11) :3328-3332
[8]   Fabrication of interconnected 1D molecular lines along and across the dimer rows on the Si(100)-(2 x 1)-H surface through the radical chain reaction [J].
Hossain, MZ ;
Kato, HS ;
Kawai, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (49) :23129-23133
[9]   Controlled fabrication of 1D molecular lines across the dimer rows on the Si(100)-(2x1)-H surface through the radical chain reaction [J].
Hossain, Z ;
Kato, HS ;
Kawai, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (43) :15030-15031
[10]   A quantum chemical study of the self-directed growth mechanism of styrene and propylene molecular nanowires on the silicon (100) 2X1 surface [J].
Kang, JK ;
Musgrave, CB .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (22) :9907-9913