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Preparation of Fe(3)O(4)-Ag Nanocomposites with Silver Petals for SERS Application

The formation of silver nanopetal-Fe(3)O(4) poly-nanocrystals assemblies and the use of the resulting hetero-nanostructures as active substrates for Surface Enhanced Raman Spectroscopy (SERS) application are here reported. In practice, about 180 nm sized polyol-made Fe(3)O(4) spheres, constituted by...

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Detalles Bibliográficos
Autores principales: Nguyen, Thi Thuy, Mammeri, Fayna, Ammar, Souad, Nguyen, Thi Bich Ngoc, Nguyen, Trong Nghia, Nghiem, Thi Ha Lien, Thuy, Nguyen Thi, Ho, Thi Anh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153338/
https://www.ncbi.nlm.nih.gov/pubmed/34068287
http://dx.doi.org/10.3390/nano11051288
Descripción
Sumario:The formation of silver nanopetal-Fe(3)O(4) poly-nanocrystals assemblies and the use of the resulting hetero-nanostructures as active substrates for Surface Enhanced Raman Spectroscopy (SERS) application are here reported. In practice, about 180 nm sized polyol-made Fe(3)O(4) spheres, constituted by 10 nm sized crystals, were functionalized by (3-aminopropyl)triethoxysilane (APTES) to become positively charged, which can then electrostatically interact with negatively charged silver seeds. Silver petals were formed by seed-mediated growth in presence of Ag(+) cations and self-assembly, using L-ascorbic acid (L-AA) and polyvinyl pyrrolidone (PVP) as mid-reducing and stabilizing agents, respectively. The resulting plasmonic structure provides a rough surface with plenty of hot spots able to locally enhance significantly any applied electrical field. Additionally, they exhibited a high enough saturation magnetization with M(s) = 9.7 emu g(−1) to be reversibly collected by an external magnetic field, which shortened the detection time. The plasmonic property makes the engineered Fe(3)O(4)-Ag architectures particularly valuable for magnetically assisted ultra-sensitive SERS sensing. This was unambiguously established through the successful detection, in water, of traces, (down to 10(−10) M) of Rhodamine 6G (R6G), at room temperature.