Applied Physics A

, Volume 76, Issue 4, pp 541–543

Self-assembly of length-tunable gold nanoparticle chains in organic solvents

  • J.H. Liao
  • K.J. Chen
  • L.N. Xu
  • C.W. Ge
  • J. Wang
  • L. Huang
  • N. Gu

DOI: 10.1007/s00339-002-1716-x

Cite this article as:
Liao, J., Chen, K., Xu, L. et al. Appl Phys A (2003) 76: 541. doi:10.1007/s00339-002-1716-x

Abstract.

The one-dimensional coagulation of gold colloidal particles dispersed in organic solvent was investigated with transmission electron microscopy. The results indicate that the length of the nanoparticle chains can be modulated by changing the concentration of the solutions. It was also demonstrated that the wetting of the substrate surface hardly influenced the morphology of the nanoparticle chains, which revealed that the particle chains had been formed in the solution before deposition on the substrates. A general theoretical interpretation is provided to explain the linear coagulation of gold colloidal particles, on the basis of the asymmetrical distribution of the charges absorbed on the surface of the gold colloidal particles, as well as the action of the solvent molecules.

PACS: 81.07.-b; 82.70.Dd; 85.65.+h; 81.16.Dn; 85.35.Gv 

Copyright information

© Springer-Verlag 2002

Authors and Affiliations

  • J.H. Liao
    • 1
  • K.J. Chen
    • 2
  • L.N. Xu
    • 1
  • C.W. Ge
    • 1
  • J. Wang
    • 1
  • L. Huang
    • 1
  • N. Gu
    • 1
  1. 1.National Laboratory of Molecular and Biomolecular Electronics, Southeast University, Nanjing, 210096, P.R. ChinaCN
  2. 2.Laboratory of Solid State Microstructures, Nanjing University, Nanjing, 210008, P.R. ChinaCN