4.3 Article

Kinetics and Mechanism of In Situ Metallization of Bulk DNA Films

Journal

NANOSCALE RESEARCH LETTERS
Volume 17, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1186/s11671-022-03658-8

Keywords

DNA; Resistive switching; Metallization

Funding

  1. Ministry of Science and Technology (MOST) in Taiwan [108-2221-E-007-101-MY2, 110-2628-E-007-006-]

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This study presents the in situ synthesis of metallic structures in a natural DNA complex bulk film by UV light irradiation and resolves the growth process of silver particles using time-resolved small-angle X-ray scattering and dielectric spectroscopy. The research provides important insights into the kinetics and mechanisms of natural DNA metallization, correlated with multi-stage switching operations in the bulk phase, paving the way for the development of versatile biomaterial composites with tunable physical properties for optical storage, plasmonics, and catalytic applications.
DNA-templated metallization is broadly investigated in the fabrication of metallic structures by virtue of the unique DNA-metal ion interaction. However, current DNA-templated synthesis is primarily carried out based on pure DNA in an aqueous solution. In this study, we present in situ synthesis of metallic structures in a natural DNA complex bulk film by UV light irradiation, where the growth of silver particles is resolved by in situ time-resolved small-angle X-ray scattering and dielectric spectroscopy. Our studies provide physical insights into the kinetics and mechanisms of natural DNA metallization, in correlation with the multi-stage switching operations in the bulk phase, paving the way towards the development of versatile biomaterial composites with tunable physical properties for optical storage, plasmonics, and catalytic applications.

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