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Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate.

Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Research Abstract Details 

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  • Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Abstract Text:

    chongyang pengChongyang Peng,yonghai songYonghai Song,gang weiGang Wei,wanxi zhangWanxi Zhang,zhuang liZhuang Li,wen-fei dongWen-Fei Dong,chongyang pengChongyang Peng,yonghai songYonghai Song,gang weiGang Wei,wanxi zhangWanxi Zhang,zhuang liZhuang Li,wen-fei dongWen-Fei Dong,

    In this article, highly rough and stable surface enhanced Raman scattering (SERS)-active substrates had been fabricated by a facile layer-by-layer technique. Unique lambda-DNA networks and CTAB capped silver nanoparticles (AgNP) were alternatively self-assembled on the charged mica surface until a desirable number of bilayers were reached. The as-prepared hybrid architectures were characterized by UV-vis spectroscopy, tapping mode atomic force microscopy (AFM) and confocal Raman microscopy, respectively. Linear increases of the maximum absorbance of DNA band with the number of bilayers present a common LBL assembly feature. The red-shift of surface plasmon of silver nanoparticles within the hybrid films was mainly due to the aggregation effect. With the increase of number of bilayers, the surface coverage of nanoparticles on the substrate became larger, as well as the rising of total amount of nanoparticles and the surface roughness of hybrid films. These rough metallic hybrid architectures could be utilized as SERS-active substrates. A significant enhanced Raman scattering effect of the adsorbed analytes, e.g., methylene blue (MB), on these hybrid films was easily exploited by the confocal Raman microscopy. The enhancement factor depended on the surface coverage of nanoparticles and number of bilayers of lambda-DNA/AgNP.

    Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Publishing Authors By Initials

    c pengC Peng,y songY Song,g weiG Wei,w zhangW Zhang,z liZ Li,wf dongWF Dong,c pengC Peng,y songY Song,g weiG Wei,w zhangW Zhang,z liZ Li,wf dongWF Dong,

    For similar natural sciences: chemistry: chemistry, physical: surface properties research abstracts see: natural sciences: chemistry: chemistry, physical: surface properties research

    PUBMED ID PMID:

    MEDLINE DATE:

    Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of colloid and interface science

    VOLUME: 317

    Page Numbers: 183-90

    Journal Abbreviation:

    ISSN: 0021-9797

    DAY: 14

    MONTH: 09

    YEAR: 2007

    Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 43125

    Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Keywords Mesh Terms:

    KEYWORDS: Surface Properties

    MESH TERMS: methods

    Chemical & Substance for Abstract: Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate. Information

    Substance Name: Silver

    Registry Number: 7440-22-4

    Grant and Affiliation Information for Self-assembly of lambda-DNA networks/Ag nanoparticles: hybrid architecture and active-SERS substrate.

    AFFILIATION: State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Graduate School of the Chinese Academy of Sciences, Chinese Academy of Sciences, Changchun 130022, PR China.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Colloid Interface Sci

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