A "grow-in-place" architecture and methodology for electrochemical synthesis of conducting polymer nanoribbon device arrays

被引:22
作者
Peng, CY
Kalkan, AK
Fonash, SJ [1 ]
Gu, B
Sen, A
机构
[1] Penn State Univ, Ctr Nanotechnol Educ & Utilizat, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
关键词
D O I
10.1021/nl048083v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fully enclosed horizontal nanochannels, in a prearranged array on a substrate and with built-in electrical contacts and chemical access regions, were used as growth templates for electrochemical synthesis of conducting polymer nanoribbons. In this "grow-in-place" approach, the nanochannel templates are part of the final array structure and remain after fabrication of the nanoribbons. The built-in electrical contacts, which provide the electrical potential for electrochemical polymerization, also remain and become contacts/interconnects to the array components. The grow-in-place architecture and methodology remove the need for template dissolution, any post-synthesis nanoribbon "grow-and-then-place" manipulation, and any post-synthesis electrical contacting. The fact that the templates are fully enclosed prohibits dendrite formation during growth, ensures precise dimensionality, and gives the encapsulation needed in any real device application. In this report the grow-in-place approach to electrochemical polymerization is used to produce polyaniline nanoribbons. These were found to be fibrils and not tubes and to grow from the central region of the growth-template cross-section and not from the template walls. Two-point and four-point electrical characterization of these polyaniline nanoribbons, obtained using the built-in electrodes, was employed to yield the true polyaniline conductivity and to assess the ohmicity of the contacting approach. Conductivity studies, done as a function of nanoribbon width, show conductivity increases as the width decreases. We also show that our grow-in-place approach may be used for chemical polymerization. However, at least for polyaniline, electrochemical polymerization is superior since it does not suffer from diffusion-limited growth and allows precise placement of the nanoribbons in the growth channel.
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收藏
页码:439 / 444
页数:6
相关论文
共 38 条
[21]   TEMPLATE-SYNTHESIZED POLYANILINE MICROTUBULES [J].
PARTHASARATHY, RV ;
MARTIN, CR .
CHEMISTRY OF MATERIALS, 1994, 6 (10) :1627-1632
[22]   Formation of nanostructured polymer filaments in nanochannels [J].
Peng, CY ;
Nam, WJ ;
Fonash, SJ ;
Gu, B ;
Sen, A ;
Strawhecker, K ;
Natarajan, S ;
Foley, HC ;
Kim, SH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (31) :9298-9299
[23]  
RAMANATHAN K, 2004, 206 EL SOC M HON HAW, P34436
[24]   Single-electron transistor made of multiwalled carbon nanotube using scanning probe manipulation [J].
Roschier, L ;
Penttilä, J ;
Martin, M ;
Hakonen, P ;
Paalanen, M ;
Tapper, U ;
Kauppinen, EI ;
Journet, C ;
Bernier, P .
APPLIED PHYSICS LETTERS, 1999, 75 (05) :728-730
[25]   OPTICAL-PROPERTIES OF POLYANILINE THIN-FILMS [J].
SCULLY, M ;
PETTY, MC ;
MONKMAN, AP .
SYNTHETIC METALS, 1993, 55 (01) :183-187
[26]   From Si source gas directly to positioned, electrically contacted Si nanowires: The self-assembling "grow-in-place" approach [J].
Shan, YH ;
Kalkan, AK ;
Peng, CY ;
Fonash, SJ .
NANO LETTERS, 2004, 4 (11) :2085-2089
[27]  
SKOTHEIM TA, 1997, HDB CONDUCTING POLYM, P34436
[28]   Electric-field assisted assembly and alignment of metallic nanowires [J].
Smith, PA ;
Nordquist, CD ;
Jackson, TN ;
Mayer, TS ;
Martin, BR ;
Mbindyo, J ;
Mallouk, TE .
APPLIED PHYSICS LETTERS, 2000, 77 (09) :1399-1401
[29]   POLARON LATTICE IN HIGHLY CONDUCTING POLYANILINE - THEORETICAL AND OPTICAL STUDIES [J].
STAFSTROM, S ;
BREDAS, JL ;
EPSTEIN, AJ ;
WOO, HS ;
TANNER, DB ;
HUANG, WS ;
MACDIARMID, AG .
PHYSICAL REVIEW LETTERS, 1987, 59 (13) :1464-1467
[30]   Electric-field-aligned growth of single-walled carbon nanotubes on surfaces [J].
Ural, A ;
Li, YM ;
Dai, HJ .
APPLIED PHYSICS LETTERS, 2002, 81 (18) :3464-3466