Journal
NANOSCALE RESEARCH LETTERS
Volume 17, Issue 1, Pages -Publisher
SPRINGER
DOI: 10.1186/s11671-022-03658-8
Keywords
DNA; Resistive switching; Metallization
Funding
- 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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