Immobilization of Gold Nanoparticles in Localized Surface Plasmon Polariton-Coupled Hot Spots via Photolytic Dimerization of Aromatic Amine Groups for SERS Detection in a Microfluidic Regime

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F22%3A43924619" target="_blank" >RIV/60461373:22310/22:43924619 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/60461373:22330/22:43924619

Výsledek na webu

<a href="https://pubs.acs.org/doi/10.1021/acsanm.1c03413" target="_blank" >https://pubs.acs.org/doi/10.1021/acsanm.1c03413</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acsanm.1c03413" target="_blank" >10.1021/acsanm.1c03413</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Immobilization of Gold Nanoparticles in Localized Surface Plasmon Polariton-Coupled Hot Spots via Photolytic Dimerization of Aromatic Amine Groups for SERS Detection in a Microfluidic Regime

Popis výsledku v původním jazyce

Plasmon-assisted chemistry is an effective tool for triggering various chemical transformations that can be performed with high spatial precision. Plasmon-triggering efficiency is ensured by a high concentration of light energy near the plasmonic surface and the resulting enhancement of the local electric field (EF). The coupling of different plasmonic nanostructures by multimodal plasmonic hot spots can significantly enhance the EF, increasing plasmon-triggering efficiency. In this work, we demonstrate that the coupling between the traveled surface plasmon polariton (SPP) wave and the localized surface plasmon (LSP) resonance can be used to effectively realize plasmon-induced organic reactions, even in hot spots between SPP- and LSP-supported Au nanostructures. The periodically modulated surface of the gold grating was used as an SPP-active plasmonic support, with spherical Au nanoparticles (AuNPs) ensuring LSP excitation. To model the chemical transformation, we utilized the dimerization of amino groups (previously grafted to Au nanostructures) with azo bridges between the AuNPs and Au grating. The reaction was performed in a microfluidic regime and resulted in AuNP immobilization on the grating surface. Experiments and theoretical studies indicated that the azo-bridge formation and AuNP immobilization occurred only under illumination with the SPP wavelength and proceeded more effectively on the grating walls (particularly the inflection points), where the EF enhancement is greatest due to LSP-SPP coupling. Created structures were subsequently demonstrated as a promising substrate for the SERS-based detection in the microfluidic regime. © 2022 American Chemical Society. All rights reserved.

Název v anglickém jazyce

Immobilization of Gold Nanoparticles in Localized Surface Plasmon Polariton-Coupled Hot Spots via Photolytic Dimerization of Aromatic Amine Groups for SERS Detection in a Microfluidic Regime

Popis výsledku anglicky

Plasmon-assisted chemistry is an effective tool for triggering various chemical transformations that can be performed with high spatial precision. Plasmon-triggering efficiency is ensured by a high concentration of light energy near the plasmonic surface and the resulting enhancement of the local electric field (EF). The coupling of different plasmonic nanostructures by multimodal plasmonic hot spots can significantly enhance the EF, increasing plasmon-triggering efficiency. In this work, we demonstrate that the coupling between the traveled surface plasmon polariton (SPP) wave and the localized surface plasmon (LSP) resonance can be used to effectively realize plasmon-induced organic reactions, even in hot spots between SPP- and LSP-supported Au nanostructures. The periodically modulated surface of the gold grating was used as an SPP-active plasmonic support, with spherical Au nanoparticles (AuNPs) ensuring LSP excitation. To model the chemical transformation, we utilized the dimerization of amino groups (previously grafted to Au nanostructures) with azo bridges between the AuNPs and Au grating. The reaction was performed in a microfluidic regime and resulted in AuNP immobilization on the grating surface. Experiments and theoretical studies indicated that the azo-bridge formation and AuNP immobilization occurred only under illumination with the SPP wavelength and proceeded more effectively on the grating walls (particularly the inflection points), where the EF enhancement is greatest due to LSP-SPP coupling. Created structures were subsequently demonstrated as a promising substrate for the SERS-based detection in the microfluidic regime. © 2022 American Chemical Society. All rights reserved.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

20501 - Materials engineering

Projekt

<a href="/cs/project/GA21-02550S" target="_blank" >GA21-02550S: Plazmonem indukované zachycení excitovaného spinového stavu v komplexech se spinovým krosoverem</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2022

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

ACS Applied Nano Materials

ISSN

2574-0970

e-ISSN

—

Svazek periodika

5

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

9

Strana od-do

1836-1844

Kód UT WoS článku

000757907900001

EID výsledku v databázi Scopus

2-s2.0-85125122835