Formation of High-Quality Self-Assembled Monolayers of Conjugated Dithiols on Gold: Base Matters

被引:94
|
作者
Valkenier, Hennie [1 ,2 ]
Huisman, Everardus H. [2 ]
van Hal, Paul A. [3 ]
de Leeuw, Dago M. [2 ,3 ]
Chiechi, Ryan C. [1 ,2 ]
Hummelen, Jan C. [1 ,2 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
[2] Univ Groningen, Zernike Inst Adv Mat, NL-9747 AG Groningen, Netherlands
[3] Philips Res Labs, NL-5656 AE Eindhoven, Netherlands
关键词
MOLECULE-METAL JUNCTIONS; BIPHENYL ETHYNYL THIOLS; OLIGO(PHENYLENE ETHYNYLENE)S; ELECTRICAL CHARACTERIZATION; CONDUCTANCE; FABRICATION; MICROSCOPY; OLIGOMERS; LENGTH; TERPHENYLDITHIOL;
D O I
10.1021/ja110358t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This Article reports a systematic study on the formation of self-assembled monolayers (SAMs) of conjugated molecules for molecular electronic (ME) devices. We monitored the deprotection reaction of acetyl protected dithiols of oligophenylene ethynylenes (OPEs) in solution using two different bases and studied the quality of the resulting SAMs on gold. We found that the optimal conditions to reproducibly form dense, high-quality monolayers are 9-15% triethylamine (Et3N) in THF. The deprotection base tetrabutylammonium hydroxide (Bu4NOH) leads to less dense SAMs and the incorporation of Bu4N into the monolayer. Furthermore, our results show the importance of the equilibrium concentrations of (di)thiolate in solution on the quality of the SAM. To demonstrate the relevance of these results for molecular electronics applications, large-area molecular junctions were fabricated using no base, Et3N, and Bu4NOH. The magnitude of the current-densities in these devices is highly dependent on the base. A value of beta = 0.15 angstrom(-1) for the exponential decay of the current-density of OPEs of varying length formed using Et3N was obtained.
引用
收藏
页码:4930 / 4939
页数:10
相关论文
共 50 条
  • [1] Self-assembled monolayers based on chelating aromatic dithiols on gold
    Garg, N
    Lee, TR
    [J]. LANGMUIR, 1998, 14 (14) : 3815 - 3819
  • [2] Rapid formation of high-quality self-assembled monolayers of dodecanethiol on polycrystalline gold under ultrasonic irradiation
    Dai, Hanyuan
    Cheng, Jiongjia
    Li, Zhiguo
    Jin, Jinc
    Bi, Shuping
    [J]. ELECTROCHIMICA ACTA, 2008, 53 (09) : 3479 - 3483
  • [3] Dielectric properties of self-assembled monolayers of dithiols
    Luo, Jiang-long
    Xia, Chen
    [J]. CHINESE JOURNAL OF CHEMICAL PHYSICS, 2006, 19 (06) : 515 - 518
  • [4] Formation of gold-methanethiyl self-assembled monolayers
    Wang, Yun
    Hush, Noel S.
    Reimers, Jeffrey R.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (47) : 14532 - +
  • [5] Self-assembled monolayers on gold of thiols incorporating conjugated terminal groups
    Reese, S
    Fox, MA
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (49): : 9820 - 9824
  • [6] New semifluorinated dithiols self-assembled monolayers on a copper platform
    Amato, Claire
    Devillers, Sebastien
    Calas, Patrick
    Delhalle, Joseph
    Mekhalif, Zineb
    [J]. LANGMUIR, 2008, 24 (19) : 10879 - 10886
  • [7] New self-assembled monolayers (SAMs) on gold derived from chelating aromatic dithiols.
    Garg, N
    Lee, TR
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 215 : U417 - U417
  • [8] Self-assembled monolayers of thiols and dithiols on gold: new challenges for a well-known system
    Vericat, C.
    Vela, M. E.
    Benitez, G.
    Carro, P.
    Salvarezza, R. C.
    [J]. CHEMICAL SOCIETY REVIEWS, 2010, 39 (05) : 1805 - 1834
  • [9] Formation of alkanethiolate self-assembled monolayers on oxidized gold surfaces
    Yan, C
    Gölzhäuser, A
    Grunze, M
    Wöll, C
    [J]. LANGMUIR, 1999, 15 (07) : 2414 - 2419
  • [10] Self-assembled monolayers of carceplexes on gold
    Huisman, BH
    Rudkevich, DM
    vanVeggel, FCJM
    Reinhoudt, DN
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (14) : 3523 - 3524