Using block copolymer micellar thin films as templates for the production of catalysts for carbon nanotube growth

被引:51
作者
Bennett, RD
Xiong, GY
Ren, ZF
Cohen, RE [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02140 USA
[2] Boston Coll, Dept Phys, Chestnut Hill, MA 02467 USA
关键词
D O I
10.1021/cm048992l
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
We report a novel approach that uses block copolymer micelles as a means to create large area arrays of iron-containing nanoclusters capable of catalyzing the growth of carbon nanotubes (CNTs). The amphiphilic block copolymer poly(styrene-block-acrylic acid) (PS-b-PAA) forms micelles in solution which are capable of self-organizing into ordered structures on surfaces. By spin-coating these solutions onto a variety of substrates. we can create. quasi-hexagonal arrays of PAA spheres within a PS matrix. The carboxylic acids groups in the PAA domains can be utilized in an ion-exchange protocol to selectively sequester iron ions.. which results in iron-containing nanoclusters that are nearly monodisperse in size (diameter similar to8 nm) and patterned at a density of approximately 10(11) particles per cm(2) . In principle, this route for synthesizing iron-containing nanoclusters offers the capability of controlling the cluster size and spacing by altering the molecular weight of the block copolymer. In this. report, we demonstrate the ability of these block-copolymer-templated iron-containing nanocluster arrays to catalyze the growth of CNTs in a thermal chemical vapor deposition (CVD) process. We present transmission electron microscope (TEM) and scanning electron microscope (SEM) images of the as-grown CNTs still attached to their growth Substrate, which allows us to characterize both the CNTs and the catalytic nanoclusters after CVD growth.
引用
收藏
页码:5589 / 5595
页数:7
相关论文
共 17 条
  • [1] Cavitated block copolymer micellar thin films: Lateral arrays of open nanoreactors
    Boontongkong, Y
    Cohen, RE
    [J]. MACROMOLECULES, 2002, 35 (09) : 3647 - 3652
  • [2] Diameter-controlled synthesis of carbon nanotubes
    Cheung, CL
    Kurtz, A
    Park, H
    Lieber, CM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (10) : 2429 - 2433
  • [3] Efficient formation of iron nanoparticle catalysts on silicon oxide by hydroxylamine for carbon nanotube synthesis and electronics
    Choi, HC
    Kundaria, S
    Wang, DW
    Javey, A
    Wang, Q
    Rolandi, M
    Dai, HJ
    [J]. NANO LETTERS, 2003, 3 (02) : 157 - 161
  • [4] Synthesis of metal nanoclusters within microphase-separated diblock copolymers: sodium carboxylate vs carboxylic acid functionalization
    Clay, RT
    Cohen, RE
    [J]. SUPRAMOLECULAR SCIENCE, 1998, 5 (1-2): : 41 - 48
  • [5] A CARBON NANOTUBE FIELD-EMISSION ELECTRON SOURCE
    DEHEER, WA
    CHATELAIN, A
    UGARTE, D
    [J]. SCIENCE, 1995, 270 (5239) : 1179 - 1180
  • [6] Storage of hydrogen in single-walled carbon nanotubes
    Dillon, AC
    Jones, KM
    Bekkedahl, TA
    Kiang, CH
    Bethune, DS
    Heben, MJ
    [J]. NATURE, 1997, 386 (6623) : 377 - 379
  • [7] HAUNG ZP, 2002, APPL PHYS A, V74, P337
  • [8] Organometallic block copolymers as catalyst precursors for templated carbon nanotube growth
    Hinderling, C
    Keles, Y
    Stöckli, T
    Knapp, HE
    de los Arcos, T
    Oelhafen, P
    Korczagin, I
    Hempenius, MA
    Vancso, GJ
    Pugin, RL
    Heinzelmann, H
    [J]. ADVANCED MATERIALS, 2004, 16 (11) : 876 - 879
  • [9] Low-temperature growth of carbon nanotubes by plasma-enhanced chemical vapor deposition
    Hofmann, S
    Ducati, C
    Robertson, J
    Kleinsorge, B
    [J]. APPLIED PHYSICS LETTERS, 2003, 83 (01) : 135 - 137
  • [10] Growth of large periodic arrays of carbon nanotubes
    Huang, ZP
    Carnahan, DL
    Rybczynski, J
    Giersig, M
    Sennett, M
    Wang, DZ
    Wen, JG
    Kempa, K
    Ren, ZF
    [J]. APPLIED PHYSICS LETTERS, 2003, 82 (03) : 460 - 462