combined electrostatic-covalent building of au nps multilayers and their size-enhanced cohesive and sers properties结合electrostatic-covalent建设非盟nps多层膜及其size-enhanced凝聚力和ser属性.pdfVIP
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combined electrostatic-covalent building of au nps multilayers and their size-enhanced cohesive and sers properties结合electrostatic-covalent建设非盟nps多层膜及其size-enhanced凝聚力和ser属性
Hindawi Publishing Corporation
Advances in Physical Chemistry
Volume 2010, Article ID 289371, 11 pages
doi:10.1155/2010/289371
Research Article
Combined Electrostatic-Covalent Building of Au NPs Multilayers
and Their Size-Enhanced Cohesive and SERS Properties
K. Mougin, S. Darwich, L. Vidal, and H. Haidara
Institut de Science des Mat´eriaux de Mulhouse, IS2M-CNRS/UHA, 15 Rue Jean Starcky, 68057 Mulhouse, France
Correspondence should be addressed to K. Mougin, karine.mougin@uha.fr
Received 21 September 2010; Revised 9 November 2010; Accepted 30 December 2010
Academic Editor: Konstantin Neyman
Copyright © 2010 K. Mougin et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Multilayers of well-ordered and close-packed 2D nanostructures of gold nanoparticles (NPs) were fabricated using a layer-by-layer
technique. Colloidal spherical Au NPs of 5 and 15 nm diameters were synthesized and, respectively, self-assembled in multilayers.
The robustness of these systems was insured by a combination of electrostatic and covalent bonds between nanoparticles and linker
molecules. The compacity of the superlattice was characterized by AFM observation and ellipsometry measurements. Evidence of
stronger cohesion of multilayers of smaller NPs size was brought by submitting the systems to sonication test. The multilayers
have also proved analytical potential when used to detect low concentration methylene blue molecules adsorbed on the Au
nanoparticles, by surface-enhanced Raman spectroscopy (SERS). The detection sensitivity of these two sized Au NPs architectures
was directly compared to an evaporated “bulk” Au thin film o
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