4.4 Article

Surface assembly and nanofabrication of 1,1,1-tris(mercaptomethyl)heptadecane on Au(111) studied with time-lapse atomic force microscopy

期刊

BEILSTEIN JOURNAL OF NANOTECHNOLOGY
卷 5, 期 -, 页码 26-35

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjnano.5.3

关键词

liquid AFM; multidentate; nanografting; nanolithography; self-assembly

资金

  1. National Science Foundation [DMR-0906873, DMR-0906727]
  2. American Chemical Society Petroleum Research Fund New Directions Program
  3. Camille Dreyfus Teacher-Scholar award
  4. Robert A. Welch Foundation [E-1320]
  5. Texas Center for Superconductivity at the University of Houston

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The solution self-assembly of multidentate organothiols onto Au(111) was studied in situ using scanning probe nanolithography and time-lapse atomic force microscopy (AFM). Self-assembled monolayers (SAMs) prepared from dilute solutions of multidentate thiols were found to assemble slowly, requiring more than six hours to generate films. A clean gold substrate was first imaged in ethanolic media using liquid AFM. Next, a 0.01 mM solution of multidentate thiol was injected into the liquid cell. As time progressed, molecular-level details of the surface changes at different time intervals were captured by successive AFM images. Scanning probe based nanofabrication was accomplished using protocols of nanografting and nanoshaving with n-alkanethiols and a tridentate molecule, 1,1,1-tris(mercaptomethyl) heptadecane (TMMH). Nanografted patterns of TMMH could be inscribed within n-alkanethiol SAMs; however, the molecular packing of the nanopatterns was less homogeneous compared to nanopatterns produced with monothiolates. The multidentate molecules have a more complex assembly pathway than monothiol counterparts, mediated by sequential steps of forming S-Au bonds to the substrate.

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